Abstract
The cornea is more than just a transparent piece of collagen. All of its five anatomical layers are essential for maintaining an avascular, anti-inflammatory and transparent state of the cornea, thus enabling good visual acuity. Besides the five conventional layers of the cornea (i.e., epithelium, Bowman’s layer, stroma, Descemet’s membrane and corneal endothelium), there are several other (partly “invisible”) structures and cell populations residing in and around the normal cornea. These include stromal and epithelial antigen-presenting cells (APCs: dendritic cells and macrophages), stromal and epithelial stem cells, limbal blood and — clinically invisible — lymphatic vessels as well as corneal nerves. All of these structures and cell populations are relevant for corneal microsurgeons in one or another aspect. In the following chapter, first normal corneal anatomy will be discussed briefly with respect to corneal surgery. Then selected corneal pathologies will be outlined with respect to surgical procedures of the cornea. Finally, pathologic aspects of certain corneal surgical procedures and aspects of corneal wound healing will be described.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Bock F, Dietrich T, Zimmermann P, Onderka J, Baier M, Cursiefen C. Antiangiogene Therapie am vorderen Augenabschnitt. Ophthalmologe 2007; 104:336–344
Bock F, Onderka J, Zahn G, Dietrich T, Bachmann B, Kruse FE, Cursiefen C. Bevacizumab is a potent inhibitor of inflammatory corneal angiogenesis and lymphangiogenesis. Invest Ophthalmol Vis Sci. 2007; 48:2545–2552
Braun M, Holbach L, Naumann GOH. Die korneale Lipofuszinose — klinisch-pathologische Untersuchung von zehn Patienten. Klin Monatsbl Augenheilkd 1997; 210:121–123
Chen JJ, Tseng SC, 1991. Abnormal corneal epithelial wound healing in partial-thickness removal of limbal epithelium. Invest. Ophthalmol. Vis. Sci. 32, 2219–2233
Chen L, Hamrah P, Cursiefen C, Jackson D, Streilein JW, Dana MR. Vascular Endothelial Growth Factor Receptor-3 (VEGFR-3) mediates dendritic cell migration to lymph nodes and induction of immunity to corneal transplants. Nature Medicine 2004; 10:813–815
Chen Z, de Paiva CS, Luo L, Kretzer FL, Pflugfelder SC, Li D-Q, 2004. Characterization of putative stem cell phenotype in human limbal epithelia. Stem Cells 22, 355–366
Cursiefen C, Küchle M, Naumann GOH. Angiogenesis in corneal diseases: Histopathology of 254 human corneal buttons with neovascularization. Cornea 1998; 17: 611–613
Cursiefen C, Küchle M, Naumann GOH. Changing indications for penetrating keratoplasty: Histopathology of 1250 corneal buttons. Cornea 1998; 17: 468–470
Cursiefen C, Hofmann-Rummelt C, Schlötzer-Schrehardt U, Fischer DC, Küchle M. Immunphänotypische Klassifizierung der makulären Hornhautdystrophie: Erstbeschreibung des Immunphänotyps I A außerhalb Saudi-Arabiens. Klin Monatsbl Augenheilkd 2000;217:118–126
Cursiefen C, Rummelt C, Küchle M. Immunohistochemical localization of VEGF, TGFa andTGFβ1 in human corneas with neovascularization. Cornea 2000; 19: 526–533
Cursiefen C, Schlötzer-Schrehardt U, Holbach M, Vieth M, Kuchelmeister K, Stolte M. Ocular findings in Fryns syndrome. Acta Ophthalmol Scand 2000; 78: 710–713
Cursiefen C, Hofmann-Rummelt C, Schlötzer-Schrehardt U, Fischer D-C, Haubeck H-D, Küchle M, Naumann GOH. Immunohistochemical classification of primary and recurrent macular corneal dystrophy in Germany. Subclassification of immunophenotype I A using a novel keratan sulfate antibody. Exp Eye Res 2001; 73: 593–600
Cursiefen C, Wenkel H, Martus P, Langenbucher A, Seitz B, Nguyen N, Küchle M, Naumann GOH. Peripheral corneal neovascularization after non-high risk-keratoplasty: influence of shortversus longtime topical steroids. Graefe’s Arch Clin Exp Ophthalmol 2001; 239: 514–521
Cursiefen C, Martus P, Nguyen NX, Langenbucher A, Seitz B, Küchle M. Corneal neovascularization after nonmechanical versus mechanical corneal trephination for non-high-risk keratoplasty. Cornea 2002; 21: 648–652
Cursiefen C, Schlötzer-Schrehardt U, Küchle M, Sorokin L, Breitender-Geleff S, Alitalo K, Jackson D. Lymphatic vessels in vascularized human corneas: immunohistochemical investigation using LYVE-1 and Podoplanin. Invest Ophthalmol Vis Sci 2002; 43: 2127–2135
Cursiefen C, Chen L, Dana MR, Streilein JW. Corneal lymphangiogenesis: Evidence, mechanisms and implications for transplant immunology. Cornea 2003; 22: 273–281
Cursiefen C, Seitz B, Dana MR, Streilein JW. Angiogenese und Lymphangiogenese in der Hornhaut: Pathogenese, Klinik und Therapieoptionen. Ophthalmologe 2003; 100:292–299
Cursiefen C, Rummelt C, Küchle M, Schlötzer-Schrehardt U. Pericyte recruitment in human corneal angiogenesis. Br J Ophthalmol 2003; 87: 101–106
Cursiefen C, Chen L, Borges L, Jackson D, D’Amore PA, Dana MR, Wiegand SJ, Streilein JW. Via bone marrow-derived macrophages, VEGF A mediates lymphand hemangiogenesis in inflammatory neovascularization. J Clin Investigation 2004; 113:1040–1050
Cursiefen C, Maruyama K, Liu Y, Chen L, Jackson D, Wiegand S, Dana MR, Streilein JW. Inhibition of hemangiogenesis and lymphangiogenesis after normal-risk corneal transplantation by neutralizing VEGF promotes graft survival. Invest Ophthalmol Vis Sci 2004;45:2666–2673.
Cursiefen C, Masli S, Ng TF, Dana MR, Bornstein P, Lawler J, Streilein JW. Roles of thrombospondin 1 and 2 in regulating spontaneous and induced angiogenesis in the cornea and iris. Invest Ophthalmol Vis Sci 2004; 45:1117–1124
Cursiefen C, Ikeda S, Nishina PM, Smith RS, Ikeda A, Jackson D, Mo JS, Chen L, Dana RM, Pytowski B, Kruse FE, Streilein JW. Spontaneous corneal hemand lymphangiogenesis in mice with destrin-mutation depend on VEGFR3-signaling. Am J Pathol 2005; 166: 1367–1377
Cursiefen C, Seitz B, Kruse FE. Neurotrophe Keratopathie: Pathogenese, Klinik und Therapie. Ophthalmologe 2005;102: 7–14
Cursiefen C, Seitz B, Kruse FE. 100 Jahre Hornhauttrabsplantation. Eine Erfolgsgeschichte mit Zukunft. Deutsches Ärzteblatt 2005:45: Seite A-3078
Cursiefen C, Chen L, Saint-Geniez M, Hamrah P, Jin Y, Rashid S, Pytowski B, Streilein JW, Dana MR. Nonvascular VEGF receptor 3 expression by corneal epithelium maintains avascularity and vision. Proc Natl Acad Sci USA. 2006; 103: 11405–11410
Cursiefen C, Maruyama M, Jackson DG, Streilein W, Kruse FE. Time-course of angiogenesis and lymphangiogenesis after brief corneal inflammation. Cornea 2006;25:443–447
Cursiefen C, Rummelt C, Neuhuber W, Kruse FE, Schroedl F. Absence of blood and lymphatic vessels in the developing human cornea. Cornea 2006; 25:722–726
Cursiefen C, Rummelt C, Kruse FE. Amniotic membrane covered bi-onlay. Br J Ophthalmol 2007; 91:841–842
Daniels JT, Dart JKG, Tuft SJ, Khaw PT, 2001. Corneal stem cells in review. Wound Rep. Reg. 9, 483–494
Davanger M, Evensen A, 1971. Role of the pericorneal papillary structure in renewal of corneal epithelium. Nature 229, 560–561
Dua HS, Azuara-Blanco A, 2000. Limbal stem cells of the corneal epithelium. Surv. Ophthalmol. 44, 415–425
Dua HS, Joseph A, Shanmuganathan VA, Jones RE, 2003. Stem cell differentiation and the effects of deficiency. Eye 17, 877–885
Goldberg MF, Bron AJ, 1982. Limbal palisades of Vogt. Trans. Am. Ophthalmol. Soc. 80, 155–171
Gottschalk K, Rummelt C, Cursiefen C. Therapierefraktäre Bindehautchemosis. Klin Monatsbl Augenheilkd 2006; 223: 696–698
Grueterich M, Espana EM, Touhami A, Ti SE, Tseng SC, 2002. Phenotypic study of a case with successful transplantation of ex vivo expanded human limbal epithelium for unilateral total limbal stem cell deficiency. Ophthalmology 109, 1547–1552
Grueterich M, Espana EM, Tseng SCG, 2003. Ex vivo expansion of limbal epithelial stem cells: amniotic membrane serving as a stem cell niche. Surv. Ophthalmol. 48, 631–646
Hamrah P, Liu Y, Zhang Q, Dana MR. The corneal stroma is endowed with a significant number of resident dendritic cells. Invest Ophthalmol Vis Sci. 2003;44:581–589.
Holbach LM, Font RL, Baehr W, Pittler SJ. HSV antigen and HSV DNA in a vascular and vascularized lesion of Hornhautstroma keratitis. Curr Eye Res 1991; 10 Suppl. 63–68
Holbach LM, Seitz B, Rummelt C, Naumann GOH. An increasing optical density of stromal lesions is associated with a decrease of detectable HSV antigen in HS-keratitis. Invest Ophthalmol Vis Sci 1992; 33: 482
Holland EJ, Schwartz GS, 1996. The evolution of epithelial transplantation for severe ocular surface disease and a proposed classification system. Cornea 15, 549–556
Huang AJ, Tseng SC, 1991. Corneal epithelial wound healing in the absence of limbal epithelium. Invest. Ophthalmol. Vis. Sci. 32, 96–105
Inatomi T, Nakamura T, Koizumi N, Sotozono C, Kinoshita S, 2005. Current concepts and challenges in ocular surface reconstruction using cultivated mucosal epithelial transplantation. Cornea. 24, S32–S38
Kenyon KR, Tseng SC, 1989. Limbal autograft transplantation for ocular surface disorders. Ophthalmology 96, 709–722
Koizumi N, Inatomi T, Suzuki T, Sotozono C, Kinoshita S, 2001. Cultivated corneal epithelial stem cell transplantation in ocular surface disorders. Ophthalmology 108, 1569–1574
Kruse FE, Reinhard T, 2001. Limbal transplantation for ocular surface reconstruction. Ophthalmologe 98, 818–831
Kruse FE, Cursiefen C, Seitz B, Voelcker HE, Naumann GOH, Holbach L. Klassifikation von Erkrankungen der Augenoeberflaeche. Teil I. Ophthalmologe 2003; 100:899–915
Küchle M, Cursiefen C, Fischer D-C, Schlötzer-Schrehardt U, Naumann GOH. Recurrent macular corneal dystrophy type II 49 years after penetrating keratoplasty. Arch Ophthalmol 1999; 117:528–531
Küchle M, Cursiefen C, Nguyen NX, Langenbucher A, Seitz B, Wenkel H, Martus P, Naumann GOH. Risk factors for corneal allograft rejection: intermediate results of a prospective normal-risk keratoplasty study. Graefe’s Arch Clin Exp Ophthalmol 2002; 240: 580–584
Lavker RM, Dong G, Cheng SZ, Kudoh K, Cotsarelis G, Sun TT, 1991. Relative proliferative rates of limbal and corneal epithelia. Implications of corneal epithelial migration, circadian rhythm, and suprabasally located DNA-synthesizing keratinocytes. Invest. Ophthalmol. Vis. Sci. 32, 1864–1875
Lavker RM, Sun T-T, 2000. Epidermal stem cells: properties, markers, and location. Proc. Natl. Acad. Sci. USA. 97, 10960–10965
Lavker RM, Tseng SCG, Sun T-T, 2004. Corneal epithelial stem cells at the limbus: looking at some old problems from a new angle. Exp. Eye Res. 78, 433–446
Lehrer MS, Sun T-T, Lavker RM, 1998. Strategies of epithelial repair: modulation of stem cell and transit amplifying cell proliferation. J. Cell Sci. 111, 2867–2875
Lindberg K, Brown ME, Chaves HV, Kenyon KR, Rheinwald JG, 1993. In vitro propagation of human ocular surface epithelial cells for transplantation. Invest. Ophthalmol. Vis. Sci. 34, 2672–2679
Maruyama K, Li M, Cursiefen C, Keino H, Tomita M, Takenaka H, Jackson DG, Losordo DW, Streilein JW. Inflammatory lymphangiogenesis arises from CD1lb+ macrophages. J Clin Invest 2005; 115:2363–2372
Müller LF, Marfurt CF, Kruse FE, Tervo T. Corneal nerves: structure, contents and function. Exp Eye Res. 2003; 76: 521–542
Naumann GOH et al. Pathologie des Auges. Berlin: Springer 1980; 2. edition, 1997
Naumann GOH, Sautter H, (Mitwirkung von Bigar F) Surgical procedures of the Cornea, chapter 7 in: “Surgical Ophthalmology 1”, Blodi FC, Mackensen G, Neubauer H. (eds.), Heidelberg-New York, Springer Verlag, 433–508, 1991
Naumann GOH. The Bowman Lecture Nr. 56, Part II: Corneal Transplantation in Anterior Segment Diseases. Eye 1995; 9:398–421
Nguyen NX, Langenbucher A, Seitz B, Graupner M, Cursiefen C, Kuchle M, Naumann GOH. Blood-aqueous barrier breakdown after penetrating keratoplasty with simultaneous extracapsular cataract extraction and posterior chamber lens implantation. Graefe’s Arch Clin Exp Ophthalmol 2001; 239: 114–117
Nguyen NX, Seitz B, Langenbucher A, Wenkel H, Cursiefen C. [Clinical aspects and treatment of immunological endothelial graft rejection following penetrating normal-risk keratoplasty]. Klin Monatsbl Augenheilkd. 2004;221:467–472.
Pellegrini G, Traverso CE, Franzi AT, Zingirian M, Cancedda R, de Luca M, 1997. Long-term restoration of damaged corneal surface with autologous cultivated corneal epithelium. Lancet 349, 990–993
Puangsricharern V, Tseng SCG, 1995. Cytologic evidence of corneal diseases with limbal stem cell deficiency. Ophthalmology 102, 1476–1485
Sangwan VS, 2002. Limbal stem cells in health and disease. Biosci. Rep. 21, 385–405
Schermer A, Galvin S, Sun T-T, 1986. Differentiation-related expression of a major 64K corneal keratin in vivo and in culture. J. Cell Biol. 103, 49–62
Schlötzer-Schrehardt U, Kruse FE. Identification and characterization of limbal stem cells. Exp Eye Res. 2005;81:247–264
Schwab IR, Reyes M, Isseroff RR, 2000. Successful transplantation of bioengineered tissue replacements in patients with ocular surface disease. Cornea 19, 421–426
Seitz B, Grüterich M, Cursiefen C, Kruse FE. Konservative und chirurgische Therapie der neurotrophen Keratopathie. Ophthalmologe 2005;102:15–26
Streilein JW. Ocular immune privilege: therapeutic opportunities from an experiment of nature. Nat Rev Immunol. 2003; 3:879–889
Sun T-T, Lavker RM, 2004. Corneal epithelial stem cells: past, presence, and future. J. Invest. Dermatol. Symp. Proc, 1–6.
Tseng SCG, 1989. Concept and application of limbal stem cells. Eye 3, 141–157
Tseng SCG, 1996. Regulation and clinical implications of corneal epithelial stem cells. Mol. Biol. Rep. 23, 47–58
Tseng SC, Meller D, Anderson DF, Touhami A, Pires RT, Grueterich M, Solomon A, Espana E, Sandoval H, Ti SE, Goto E, 2002. Ex vivo preservation and expansion of human limbal epithelial stem cells on amniotic membrane for treating corneal diseases with total limbal stem cell deficiency. Adv. Exp. Med. Biol. 506, 1323–1334
Vinh L, Nguyen N, Martus P, Seitz B, Kruse FE, Cursiefen C. Surgery-related factors influencing corneal neovascularization after low-risk keratoplasty. Am J Ophthalmol 2006; 141:260–266
References
Alvarado J, Murphy C, Polansky J, Juster R. Age-related changes in trabecular meshwork cellularity. Invest Ophthalmol Vis Sci 1981; 21: 714–727
Auffarth GU, Blum M, Faller U, Tetz MR, Völcker HE. Relative anterior microphthalmos: morphometric analysis and its implications for cataract surgery. Ophthalmology 2000; 107: 1555–1560
Auffarth GU, Voelcker H-E. Cataract surgery in 79 patients with relative anterior microphthalmus (RAM). A review of anatomy, associated pathology and complications. Klin Monatsbl Augenheilk: 2006;216(6):369
CAT-1520102 Trabeculectomy Study Group, Khaw P, Grehn F, Hollo G, Overton B, Wilson R, Vogel R, Smith Z. A pahse III study of subconjunctival human anti-transforming growth factor beta (2) monoclonal antibody (CAT-152) to prevent scarring after first-time trabeculectomy. Ophthalmology 2007 Oct; 114(10):1822–1830
Debry PW, Perkins Trabekelwerk, Heatley G, Kaufmann P, Brumback LC. Incidence of late-onset bleb-related complications following trabeculectomy with mitomycin. Arch Ophthalmol 2002; 120:297–300
Grierson I, Howes RC, Wang Q. Age-related changes in the canal of Schlemm. Exp Eye Res 1984; 39: 505–512
He M, Foster PJ, Johnson GJ, Khaw PT. Angle-closure glaucoma in East Asia and European people. Different diseases? Eye 2006; 20:3–12
Holz HA, Lim MC. Glaucoma lasers: a Review of the Newer Techniques. Curr Opin Ophthalmol 2005; 16:89–93
Jonas JB, Budde WM, Panda-Jonas S. Ophthalmoscopic evaluation of the optic nerve head. Surv Ophthalmol 1999; 43:293–320
Jonas JB, Budde WM, Lang PJ. Parapapillary atrophy in the chronic open-angle glaucomas. Graefes Arch Clin Exp Ophthalmol 1999; 237: 793–799
Karlsberg, AMA Archiv Ophthalmology 1979: 86:287: Wilmer 292–294
Khaw PT, Occleston NL, Schultz G, Grierson I, Sherwood MB, Larkin G. Activation and suppression of fibroblast function. Eye 1994; 8(Pt 2): 188–195
Knorr HLJ, Jünemann A, Händel A, Strahwald H, Naumann GOH. Morphometrische und qualitative Veränderungen des Hornhautendothels beim Pseudoexfoliationssyndrom. Fortschr Ophthalmol 1991; 88: 786–789
Küchle M, Mardin C, Nguyen NX, Martus P, Naumann GOH. Quantification of Aqueous Melanin Granules in Primary Pigment Dispersion Syndrome. Am J Ophthalmol 1998; 126: 425–431
Küchle M, Nguyen NX, Mardin CY, Naumann G.O.H. Effect of neodymium:YAG laser iridotomy on number of aqueous melanin granules in primary pigment dispersion syndrome. Graefes Arch Clin Exp Ophthalmol. 2001 Jul;239(6):411–415
Kwong YY, Tham CC, Leung DY, Lam DS. Scleral perforation following diode laser transscleral cyclophotocoagulation. Eye 2006; 20: 1316–1317
Mardin CY, Küchle M, Nguyen NX, Martus P, Nauman GOH. Quantification of Aqueous Melanin Granules, Intraocular Pressure and Glaucomatous Damage in Primary Pigment Dispersion Syndrome. Ophthalmology 2000; 107: 435–440
Quigley HA. New paradigms in the mechanisms and management of glaucoma. Eye, 2005; 19:1241–1248
Rummelt V, Naumann GOH. Cystic Epithelial Ingrowth after Goniotomy for Congenital Glaucoma. J Glaucoma 1997; 6: 353–356
Ruprecht KW, Naumann GOH. Unilateral secondary open-angle glaucoma with idiopathically dilated episcleral vessels. Klin Monatsbl Augenheilkd 1984; 184:23–27
Schlötzer-Schrehardt U, Naumann GOH. Trabecular meshwork in pseudoexfoliation syndrome with and without open-angle glaucoma. A morphometric, ultrastructural study. Invest Ophthalmol Vis Sci 1995; 36: 1750–1764
References
Braun UC, Rummelt V, Naumann GOH. Diffuse maligne Melanome der Uvea. Eine klinisch-histopathologische Studie über 39 Patienten. Klin Monatsbl Augenheilkd 1998; 213: 1–10
Hinzpeter EN, Demeler U, Naumann G. Iriswundheilung nach zweifacher Naht einer experimentellen Iridotomie I. Lichtmikroskopische Betrachtungen am Kaninchen Albrecht v Graefes Arch Ophthmol 1974; 191: 215–229
Hinzpeter EN, Ortbauer R, Naumann G. Healing of a sutured iridotomy in man Ophthalmologica 1974; 169: 390–396
Jünemann A, Gusek GC, Naumann GOH Optische Sektoriridektomie: Eine Alternative zur perforierenden Keratoplastik bei Petersscher Anomalie Klin Monatsbl Augenheilkd 1996; 209: 117–124
Jünemann A, Holbach L, Naumann GOH. Leiomyom der Iris Klin Monatsbl Augenheilkd 1992; 201: 322–324
Küchle M, Naumann GOH. Varixknoten der Iris mit SpontanRegression Klin Monatsbl Augenheilkd 1992; 200:233–236
Mühlenweg I, Naumann GOH. Sekundäres Pigmentdispersions-Syndrom nach medikamentöser Dauer-Mydriasis über 24 Jahren Klin Monatsbl Augenheilkd 1981; 178:24–25
Naumann G, Font RL, Zimmerman LE. Primary Rhabdomyosarcoma of the Iris. Am J Ophthalmol 1972; 74:110–118
Naumann G, Ruprecht KW. Xanthom der Iris Ophthalmologica 1972; 164:293–305
Taban M, Behrens A, Newcomb RL, Nobe MY, Saedi G, Sweet PM, McDonnell PJ. Acute endophthalmitis following cataract surgery. Arch Ophthalmol 2005; 123: 613–620
Tetsumoto K, Küchle M, Naumann GOH. Late Histopathological Findings of Neodymium: YAG Laser Iridotomies in Humans. Arch Ophthalmol 1992; 110: 1119–1123
References
Cursiefen C, Schlötzer-Schrehardt U, Holbach LM, Naumann GOH. Adenoma of the nonpigmented ciliary epithelium mimicking a malignant melanoma of the iris. Arch Ophthalmol 1999; 117: 113–116
Enoch JM. Retinal receptor orientation. Am J Optom Physiol Optics 1975; 52:375
Groh MJM, Nguyen NX, Küchle M, Naumann GOH. Umwandlung der zystischen in eine diffuse Epithelinvasion durch Laser Zysteneröffnung. Bericht über 4 Patienten. Klin Monatsbl Augenheilkd 2002; 219: 37–39
Hillemann J, Naumann G. [Benign epithelioma (Fuchs) of the ciliary body] Ophthalmologica. 1972;164(4):321–325 (in German)
Holbach L, Völcker HE, Naumann GOH. Malignes teratoides Medulloepitheliom des Ziliarkörpers und saures Gliafaserprotein-Klinische, histochemische und immunhistochemische Befunde. Klin Monatsbl Augenheilkd 1985; 187: 282–286
Jonas JB, Groh MJM, Rummelt V, Naumann GOH. Rhegmatogenous retinal detachment after block excision of epithelial implantation cysts and tumors of the anterior uvea. Ophthalmology 1999; 106: 1942–1946
Küchle M, Holbach L, Schlötzer-Schrehardt U, Naumann GOH. Schwannoma of the ciliary body treated by block excision. Br J Ophthalmol 1994; 78: 397–400
Küchle M, Naumann GOH. Direct Cyclopexy for Traumatic Cyclodialysis with Persisting Hypotony Report in 29 Consecutive Patients Ophthalmology 1995; 102: 322–333
Küchle M, Naumann GOH. Mucogenic Secondary Open-Angle Glaucoma in Diffuse Epithelial Ingrowth Treated by Block-Excision. Am J Ophthalmol 1991; 111: 230–234
Machemer R (1972) Vitrectomy. A pars plana approach. Grune & Stratton, New York, pp 1–136
Naumann G. Über pigmentierte Naevi der Aderhaut und des Ciliarkörpers (eine klinische und histopathologische Untersuchungsreihe). Adv Ophthalmol 1970; 23: 187–282
Naumann GOH. Surgery of the Ciliary Body, chapter 3 in: Koch DD, Spaeth GL (eds.) Vol II “ Cornea Glaucoma Lens ” in: “0Atlas of Ophthalmic Surgery” (3 Vol), Heilmann K, Paton D. (eds), Stuttgart, Thieme Verlag, 3.1–3.40, 1987
Naumann G, Green WR. Spontaneous nonpigmented iris cysts. Arch Ophth 1967; 78: 496–500
Naumann G, Font RL, Zimmerman LE. Primary Rhabdomyosarcoma of the Iris. Am J Ophthalmol 1972; 74: 110–118
Naumann G. Blockexcision intraokularer Prozesse I. Tumoren der vorderen Uvea. Klin Monatsbl Augenheilkd 1975; 166: 436–448
Naumann GOH, Völcker HE, Lerche W. Adenom des pigmentierten Ziliarepithels. Albrecht v. Graefes Arch Klin exp Ophthalmol 1976; 198: 245
Naumann G, Völcker HE. Blockexcision intraokularer Prozesse II. Epitheleinwachsung in den vorderen Augenabschnitten. Klin Monatsbl Augenheilkd 1975; 166: 448–457
Naumann GOH, Völcker HE. Direkte Zyklopexie zur Behandlung des persistierenden Hypotonie-Syndroms infolge traumatischer Zyklodialyse. Klin Monatsbl Augenheilkd 1981; 179:266–270
Naumann GOH, Rummelt V. Block Excision of Tumors of the Anterior Uvea. Report on 68 Consecutive Patients. Ophthalmology 1996; 103: 2017–2028
Naumann GOH, Rummelt V. Block-excision of cystic and diffuse epithelial ingrowth of the anterior chamber. Report on 32 consecutive patients. Arch Ophthalmol 1992; 110: 223–227; Arch Ophthalmol 1992; 10: 214–218 (see also Chinese and Spanish editions)
Naumann GOH, Rummelt V. Congenital nonpigmented epithelial iris cyst removed by block-excision. Graefes Arch Clin Exp Ophthalmol. 1990; 228: 392–397
Rummelt V, Naumann GOH, Folberg E, Weingeist T. Surgical management of melanocytoma of the ciliary body with extrascleral extension. Report on 4 patients. Am J Ophthalmol 1994; 117: 169–176
Rummelt V, Naumann GOH. Block excision of congenital and infantile nonpigmented epithelial iris cysts — Report on 8 infants. Ger J Ophthalmol 1992; 1: 361–366
Rummelt V, Naumann GOH. Blockexzision mit tektonischer Korneoskleralplastik wegen zystischer und/oder diffuser Epithelinvasion des vorderen Augensegments (Bericht über 51 konsekutive Patienten, 1980—1996). Klin Monatsbl Augenheilkd 1997; 211: 312–323
Rummelt V, Rummelt C, Naumann GOH. Congenital Nonpigmented Epithelial Iris Cyst after Amniocentesis Ophthalmology. 1993; 100: 776–781
Schlötzer-Schrehardt U, Jünemann A, Naumann GOH. Mitochondria-rich epithelioid leiomyoma of the ciliary body. Arch Ophthalmol 2002; 120: 77–82
Viestenz A, Küchle M, Naumann GOH. Blockexzision der Epithelinvasion nach Kataraktoperation-Bericht über 15 Patienten. Klin Monatsbl Augenheilkunde 2003; 220: 465–470
Völcker HE, Enke P. Diffuse endothelialization of a cyclodialysis cleft: a light and electron microscopic study. Klin Monatsbl Augenheilkd 1983 Sep;183(3):195–200 (in German)
Zagórski Z, Shrestha HG, Lang GK, Naumann GOH. Sekundärglaukome durch intraokulare Epithelinvasion. Klin Monatsbl Augenheilkd 1988; 192: 16–20
References
Apple DJ. Über angeborene Kolobome. Klin Mbl Augenheilk 1979; 174:649–651
Asano N, Schlötzer-Schrehardt U, Dörfler S, Naumann GOH. Ultrastructure of contusion cataract. Arch Ophthalmol 1995; 113:210–215
Assia EI, Apple DJ, Morgan RC, Legier UF, Brown SJ. The relationship between the stretching capability of the anterior capsule and zonules. Invest Ophthalmol Vis Sci 1991; 32: 2835–2839
Assia EI, Apple DJ. Side-view analysis of the lens. I. The crystalline lens and the evacuated bag. Arch Ophthalmol 1992a; 110:89–93
Assia EI, Apple DJ. Side-view analysis of the lens. II. Positioning of intraocular lenses. Arch Ophthalmol 1992b; 110: 94–97
Barraquer J. Enzymatic zonulolysis in lens extraction. Arch Ophthalmol 1961; 66: 6–11
Barraquer RI, Michael R, Abreu R, Lamarca J, Tressera F. Human lens capsule thickness as a function of age and location along the sagittal lens perimeter. Invest Ophthalmol Vis Sci 2006; 47: 2053–2060
Bartholomew RS. Lens displacement associated with pseudocapsular exfoliation. A report on 19 cases in the southern Bantu. Br J Ophthalmol 1970; 54:744–750
Benedek GB. Why is the lens transparent? Nature 1983; 302:383–384
Berman ER. Biochemistry of cataracts. In: Garner A, Klintworth GK, Eds. Pathobiology of Ocular Disease. A Dynamic Approach. New York: Marcel Dekker Inc, 1994
Bourne RR, Minassian DC, Dart JK, Rosen P, Kaushal S, Wingate N. Effect of cataract surgery on the corneal endothelium: modern phacoemulsification compared with extracapsular cataract surgery. Ophthalmology 2004; 111: 679–685
Bron AJ, Vrensen GFJM, Koretz J, Maraini G, Harding JJ. The ageing lens. Ophthalmologica 2000; 214: 86–104
Burian HM, von Noorden GK, Ponseti IV. Chamber angle anomalies in systemic connective tissue disorders. Arch Ophthalmol 1960; 64: 671–680
Cashwell LF Jr, Holleman IL, Weaver RG, van Rens GH. Idiopathic true exfoliation of the lens capsule. Ophthalmology 1989; 96: 348–351
Cross HE, Jensen AD. Ocular manifestations in the Marfan syndrome and homocystinuria. Am J Ophthalmol 1973; 75:405–420
Cruysberg JR, Pinckers A. Ectopia lentis et pupillae in three generations. Br J Ophthalmol 1995; 79: 135–138
Cugati S, Mitchell P, Rochtchina E, Tan AG, Smith W, Wang JJ. Cataract surgery and the 10-year incidence of age-related maculopathy: the Blue Mountains Eye Study. Ophthalmology 2006; 113:2020–2025
Dawczynski J, Strobel J. “The aging lens” — neue Konzepte zum Alterungsprozess der Linse. Ophthalmologe 2006; 103: 759–764
Donnenfeld ED. Eyenet (Feb) 2007, 29–30
Erie JC, Raecker MA, Baratz KH, Schleck CD, Burke JP, Robertson DM. Risk of retinal detachment after cataract extraction, 1980–2004: a population-based study. Ophthalmology 2006; 113:2026–2032
Eshagian J. Human posterior subcapsular cataracts. Trans Ophthalmol Soc UK 1982; 102:364–368
Fankhauser F, Roussel P, Steffen J, van der Zypen E, Chrenkova A. Clinical studies on the efficiency of high power laser radiation upon some structures of the anterior segment of the eye. First experiences of the treatment of some pathological conditions of the anterior segment of the human eye by means of a Q-switched laser system. Int Ophthalmol 1981; 3: 129–139
Farnsworth PN, Shyne SE. Anterior zonular shifts with age. Exp Eye Res 1979; 28: 291–297
Ferguson VM, Spalton DJ. Continued breakdown of the blood aqueous barrier following cataract surgery. Br J Ophthalmol 1992; 76: 453–456
Fisher RF, Pettet BE. The postnatal growth of the capsule of the human crystalline lens. J Anat 1972; 112: 207–214
Font RL, Brownstein S. A light and electron microscopic study of anterior subcapsular cataracts. Am J Ophthalmol 1974; 78:972–984
Freissler K, Küchle M, Naumann GOH. Spontaneous dislocation of the lens in pseudoexfoliation syndrome. Arch Ophthalmol 1995; 113: 1095–1096
Frezzotti R, Caporossi A, Mastrangelo D, Hadjistilianou T, Tosi P, Cintorino M, Minacci C. Pathogenesis of posterior capsular opacification. Part II: Histopathological and in vitro culture findings. J Cataract Refract Surg 1990; 16: 353–360
Gibbs ML, Jacobs M, Wilkie AOM, Taylor D. Posterior lenticonus: clinical patterns and genetics. J Pediatr Ophthalmol Strabismus 1993; 30:171–175
Goldberg MF. Persistent fetal vasculature (PFV): an integrated interpretation of signs and symptoms associated with persistent hyperplastic primary vitreous (PHPV). LIV Edward Jackson Memorial Lecture. Am J Ophthalmol. 1997 Nov; 124(5):587–626
Goldstein LE, Muffat JA, Cherny RA, Moir RD, Ericsson MH, Huang X, Mavros C, Coccia JA, Faget KY, Fitch KA, Masters CL, Tanzi RE, Chylack LT, Bush AI. Cytosolic beta-amyloid deposition and supranuclear cataracts in lenses from people with Alzheimer’s disease. Lancet 2003; 361(9365): 1258–1265
Guggenmoos-Holzmann I, Engel B, Henke V, Naumann GOH. Cell density of human lens epithelium in women higher than in men. Invest Ophthalmol Vis Sci 1989; 30:330–332
Guzek JP, Holm M, Cotter JB, Cameron JA, Rademaker WJ, Wissinger DH, Tonjum AM, Sleeper LA. Risk factors for intraoperative complications in 1000 extracapsular cataract cases. Ophthalmology 1987; 94: 461–466
Hagee MJ. Homocystinuria and ectopia lentis. J Am Optom Assoc 1984; 55: 269–276
Halbert SP, Manski W. Biological aspects of autoimmune reactions in the lens. Invest Ophthalmol 1965; 4:516–530
Hayashi H, Hayashi K, Nakao F, Hayashi F. Anterior capsule contraction and intraocular lens dislocation in eyes with pseudoexfoliation syndrome. Br J Ophthalmol 1998; 82: 1429–1432
Hockwin O. Scheimpflug photography of the lens. Fortschr Ophthalmol 1989; 84: 304–311
Hockwin O. Biochemistry of the lens. Retrospect of thematic and methodologic developments, prospects for future research. Klin Monatsbl Augenheilkd 1993; 202: 544–551
Hyams M, Mathalone N, Herskovitz M, Hod Y, Israeli D, Geyer O. Intraoperative complications of phacoemulsification in eyes with and without pseudoexfoliation. J Cataract Refract Surg 2005; 31: 1002–1005
Jehan FS, Mamalis N, Crandall AS. Spontaneous late dislocation of intraocular lens within the capsular bag in pseudoexfoliation patients. Ophthalmology 2001; 108: 1727–1731
Jensen AD, Cross HE, Paton D. Ocular complications in the Weill-Marchesani syndrome. Am J Ophthalmol 1974; 77: 261–269
Jünemann A, Küchle M, Händel A, Naumann GOH. Kataraktchirurgie bei Nanophthalmus mit einer Bulbuslänge unter 20,5 mm. Klin Monatsbl Augenheilkd 1998; 212: 13–22
Kainulainen K, Karttunen L, Puhakka L, Sakai L, Peltonen L. Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome. Nat Genet 1994; 6:64–69
Karim AKA, Jacob TJC, Thompson GM. The human anterior lens capsule: cell density, morphology, and mitotic index in normal and cataractous lenses. Exp Eye Res 1987; 45:865–874
Karp CL, Fazio JR, Culbertson WW, Green WR. True exfoliation of the lens capsule. Arch Ophthalmol 1999; 117: 1078–1080
Kelman CD. Phaco-emulsification and aspiration. A new technique of cataract removal. A preliminary report. Am J Ophthalmol 1967; 64: 23–35
Kelman CD. Symposium: Phacoemulsification. History of emulsification and aspiration of senile cataracts. Trans Am Acad Ophthalmol Otolaryngol 1974; 78: OP5–13
Khalil M, Saheb N. Posterior lenticonus. Ophthalmology 1984; 91: 1429–1430
Konofsky K, Naumann GOH, Guggenmoos-Holzmann I. Cell density and sex chromatin in lens epithelium of human cataracts. Quantitative studies in flat preparation. Ophthalmology 1987; 94:875–880
Krag S, Olsen T, Andreassen TT. Biomechanical characteristics of the human anterior lens capsule in relation to age. Invest Ophthalmol Vis Sci 1997; 38: 357–363
Krag S, Andreassen TT. Mechanical properties of the human posterior lens capsule. Invest Ophthalmol Vis Sci 2003; 44: 691–696
Küchle M, Amberg A, Martus P, Nguyen NX, Naumann GOH. Pseudoexfoliation syndrome and secondary cataract. Br J Ophthalmol 1997; 81: 862–866
Kuszak JR, Ennesser CA, Umlas J et al. The ultrastructure of fiber cells in primate lenses: A model for studying membrane senescence. J Ultrastruct Mol Struct Res 1988; 100:60–74
Kuwabara T. The maturation of the lens cell: a morphologic study. Exp Eye Res 1975; 20:427–443
Lang GK, Naumann GOH. Zur Klinik und Differentialdiagnose des Lentiglobus posterior (Bericht über vier Kinder). Klin Monatsbl Augenheilkd 1983; 183: 489–492
Lee B, Godfrey M, Vitale E et al. Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes. Nature 1991; 352:330–334
Lundström M, Wejde G, Steveni U et al. Endophthalmitis after Cataract Surgery: A Nation-wide study. Ophthalmology 2007; 114:866–870
Malbran ES, Croxatto JO, D’Alessandro C, Charles DE. Genetic spontaneous late subluxation of the lens. A study of two families. Ophthalmology 1989; 96: 223–229
Maloof AJ, Pandey SK, Neilson G, Milverton EJ. Selective death of lens epithelial cells using demineralized water and Triton X-100 with PerfectCapsule sealed capsule irrigation: a histological study in rabbit eyes. Arch Ophthalmol 2005; 123: 1378–1384
Marak GE Jr. Phacoanaphylactic endophthalmitis. Surv Ophthalmol 1992; 36:325–333
Marshall J, Beaconsfield M, Rothery S. The anatomy and development of the human lens and zonules. Trans Ophthalmol Soc UK 1982; 102 Pt 3: 423–440
Maumenee IH. The eye in the Marfan syndrome. Trans Am Ophthalmol Soc 1981; 79:684
Mencucci R, Ponchietti C, Virgili G, Giansanti F, Menchini U. Corneal endothelial damage after cataract surgery: Microincision versus standard technique. J Cataract Refract Surg 2006; 32: 1351–1354
Mohan PS, Spiro RG. Macromolecular organization of basement membranes. Characterization and comparison of glomerular basement membrane and lens capsule components by immunochemical and lectin affinity procedures. J Biol Chem 1986; 261:4328–4336
Moroi SE, Lark KK, Sieving PA, Nouri-Mahdavi K, Schlötzer-Schrehardt U, Katz GJ, Ritch R. Long anterior zonules and pigment dispersion. Am J Ophthalmol 2003;136:1176–1178
Mudd SH, Finkelstein JD, Irreverre F et al. Homocystinuria: an enzymatic defect. Science 1964; 143:1443–1445
Naumann GOH, Ortbauer R, Witzenhausen R. Candida albicans-endophthalmitis nach Kataraktextraktion. Ophthalmologica 1971; 162: 160–166
Naumann GOH, Küchle M, Schönherr U. Pseudoexfoliation syndrome as a risk factor for vitreous loss in extracapsular cataract extraction. Fortschr Ophthalmol 1989; 86:543–545
Nelson LB, Maumenee IH. Ectopia lentis. Surv Ophthalmol 1982; 27: 143–160
Nemet AY, Assia EI, Apple DJ, Barequet IS. Current concepts of ocular manifestations in Marfan syndrome. Surv Ophthalmol 2006; 51: 561–575
Ohrloff C, Hockwin O. Lens metabolism and aging: enzyme activities and enzyme alterations in lenses of different species during the process of aging. J Gerontol 1983; 38: 271–277
Pau H, Novotny GEK. Ultrastructural investigations on anterior capsular cataract. Cellular elements and their relationship to basement membrane and collagen synthesis. Graefes Arch Clin Exp Ophthalmol 1985; 223:41–46
Raviola G. The fine structure of the ciliary zonule and ciliary epithelium. With special regard to the organization and insertion of the zonular fibers. Invest Ophthalmol 1971; 10: 851–869
Resnikoff S, Pascolini D, Etya’ale D, Kocur I, Pararajasegaram R, Pokharel GP, Mariotti SP. Global data on visual impairment in the year 2002. Bull World Health Organ 2004; 82: 844–851
Rohen JW. Scanning electron microscopic studies of the zonular apparatus in human and monkey eyes. Invest Ophthalmol Vis Sci 1979; 18:133–144
Saber HR, Butler TJ, Cottrell DG. Resistance of the human posterior lens capsule and zonules to disruption. J Cataract Refract Surg 1998; 24: 536–542
Sakabe I, Oshika T, Lim SJ, Apple DJ. Anterior shift of zonular insertion onto the anterior surface of human crystalline lens with age. Ophthalmology 1998; 105: 295–299
Schlötzer-Schrehardt U, Naumann GOH. A histopathologic study of zonular instability in pseudoexfoliation syndrome. Am J Ophthalmol 1994; 118:730–743
Schneider H, Guthoff R. Evidenzbasierte Beobachtungen zu akkommodativen Kunstlinsen. Klin Monatsbl Augenheilkd 2005:222:357–360
Seland JH. The lens capsule and zonulae. Acta Ophthalmol Suppl. 1992; 205: 7–12
Skuta GL, Parrish RK 2nd, Hodapp E, Forster RK, Rockwood EJ. Zonular dialysis during extracapsular cataract extraction in pseudoexfoliation syndrome. Arch Ophthalmol 1987; 105: 632–634
Sommer A. Cataracts as an epidemiologic problem. Am J Ophthalmol 1977; 83:334–339
Stark WJ, Streeten BW. The anterior capsulotomy of extracapsular cataract extraction. Ophthalmic Surg 1984; 15: 911–917
Stirling RJ, Griffiths PG. Scanning EM studies of normal human lens fibres and fibres from nuclear cataracts. Eye 1991; 5:86–89
Streeten BW, Robinson MR, Wallace R, Jones DB. Lens capsule abnormalities in Alport’s syndrome. Arch Ophthalmol 1987;105:1693–1697
Taban M, Behrens A, Newcomb RL, Nobe MY, Saedi G, Sweet PM, McDonnell PJ. Acute endophthalmitis following cataract surgery. Arch Ophthalmol 2005; 123: 613–620
Thylefors B. Avoidable blindness. Bull World Health Organ 1999; 77: 453
Tripathi RC, Tripathi BJ. Lens morphology, aging, and cataract. J Gerontol 1983; 38:258–270
Tseng SH, Yen JS, Chien HL. Lens epithelium in senile cataract. J Formos Med Assoc 1994; 93:93–98
Volcker HE. Kontusionskatarakt und Linsenluxation. Fortschr Ophthalmol 1984; 81:308–311
von Below H, Wilk CM, Schaal KP, Naumann GOH. Rhodococcus luteus and Rhodococcus erythropolis chronic endophthalmitis after lens implantation. Am J Ophthalmol 1991; 112:596–597
von Sallmann L, Grimes P, McElvain N. Aspects of mitotic activity in relation to cell proliferation in the lens epithelium. Exp Eye Res 1962; 1:449–456
Vrensen GF. Aging of the human eye lens — a morphological point of view. Comp Biochem Physiol A Physiol 1995; 111: 519–532
Vrensen GF, Kappelhof J, Willekens B. Morphology of the aging human lens. Lens Eye Tox Res 1990; 7: 1–30
Wallace RN, Streeten BW, Hanna RB. Rotary shadowing of elastic system microfibrils in the ocular zonule, vitreous, and ligamentum nuchae. Curr Eye Res 1991; 10: 99–109
Wang JJ, Klein R, Smith W, Klein BE, Tomany S, Mitchell P. Cataract surgery and the 5-year incidence of late-stage age-related maculopathy: pooled findings from the Beaver Dam and Blue Mountains eye studies. Ophthalmology 2003; 110: 1960–1967
Weale RA. The accommodation of lens implants. Ophthalmic Res 2005; 37: 156–158
References
Aaberg TM, Blair CJ, Gass JD. Macular holes. Am J Ophthalmol. 1970; 69: 555–562
Abdelsalam A, Del Priore L, Zarbin MA. Drusen in age-related macular degeneration: pathogenesis, natural course, and laser photocoagulation-induced regression. Surv Ophthalmol. 1999; 44: 1–29
Abdel-Meguid A, Lappas A, Hartmann K, Auer F, Schräge N, Thumann G and Kirchhof B. One year follow up of macular translocation with 360 degree retinotomy in patients with age related macular degeneration. Br J Ophthalmol 2003; 87: 615–621
Abrams GW, Azen SP, McCuen BW, Flynn HW, Jr., Lai MY and Ryan SJ. Vitrectomy with silicone oil or long-acting gas in eyes with severe proliferative vitreoretinopathy: results of additional and long-term follow-up. Silicone Study report 11. Arch Ophthalmol 1997; 115: 335–344
Adelberg DA, del Priore LV, Kaplan HJ. Surgery for subfoveal membranes in myopia, angioid streaks, and other disorders. Retina. 1995; 15: 198–205
Aiello LP, Northrup JM, Keyt BA, Takagi H, Iwamoto MA. Hypoxic regulation of vascular endothelial growth factor in retinal cells. Arch Ophthalmol. 1995; 113: 1538–1544
Ainsworth JR, Damato BE, Lee WR, Alexander WD. Follicular thyroid carcinoma metastatic to the iris: a solitary lesion treated with iridocyclectomy. Arch Ophthalmol. 1992; 110: 19–20
Aisenbrey S, Lafaut BA, Szurman P, Grisanti S, Luke C, Krott R, Thumann G, Fricke J, Neugebauer A, Hilgers RD, Esser P, Walter P and Bartz-Schmidt KU. Macular translocation with 360 degrees retinotomy for exudative age-related macular degeneration. Arch Ophthalmol 2002; 120: 451–459
Al-Abdulla NA, Thompson JT, Sjaarda RN. Results of macular hole surgery with and without epiretinal dissection or internal limiting membrane removal. Ophthalmology. 2004; 111: 142–149
Algvere PV, Berglin L, Gouras P, Sheng Y. Transplantation of fetal retinal pigment epithelium in age-related macular degeneration with subfoveal neovascularization. Graefes Arch Clin Exp Opththalmol. 1994; 232: 707–716
Allinson RW. Adjuvant 5-FU and heparin prevent PVR. Ophthalmology 2002; 109: 829–830
Ambati J, Arroyo JG. Postoperative complications of scierai buckling surgery. Int. Ophthalmol. Clin. 2000; 40:175–185
Andersen SR, Warburg M. Nome’s disease: congenital bilateral pseudotumor of the retina with recessive X-chromosomal inheritance; preliminary report. Arch Ophthalmol. 1961; 66: 614–618
An International Classification of Retinopathy of Prematurity. II. The classification of retinal detachment. The International Committee for the Classification of the Late Stages of Retinopathy of Prematurity. Arch Ophthalmol. 1987; 105: 906–912
An International Classification of ROP revisited. The International Committee for the Classification of the Late Stages of Retinopathy of Prematurity. Arch Ophthalmol 2005; 123; 991–999
An International Classification of ROP. The International Committee for the Classification of the Late Stages of Retinopathy of Prematurity. Arch Ophthalmol 1984; 102: 1130–1134
Apple DJ, Federman JL, Krolicki TJ, Sims JC, Kent DG, Hamburger HA, Smiddy WE, Cox MS Jr, Hassan TS, Compton SM, Thomas SG. Irreversible silicone oil adhesion to silicone intraocular lenses. A clinicopathologic analysis. Ophthalmology. 1996; 103: 1555–1561
Apushkin MA, Fishman GA, Rajagopalan AS. Fundus findings and longitudinal study of visual acuity loss in patients with X-linked retinoschisis. Retina. 2005; 25: 612–618
Apushkin MA, Fishman GA, Janowicz MJ. Correlation of optical coherence tomography findings with visual acuity and macular lesions in patients with X-linked retinoschisis. Ophthalmology. 2005;113: 495–501
Archer DB. Bowman Lecture 1998. Diabetic retinopathy: some cellular, molecular and therapeutic considerations. Eye. 1999 Aug; 13:497–523
Archer DB. Doyne Lecture. Responses of retinal and choroidal vessels to ionising radiation. Eye. 1993; 7: 1–13
Asaria RHY, Kon CH, Bunce C, Charteris DG, Wong D, Khaw PT, Aylward GW. Adjuvant 5-fluorouracil and heparin prevents proliferative vitreoretinopathy: results from a randomized, double-blind, controlled clinical trial. Ophthalmology 2001; 108: 1179–1183
Ashton, N. Oxygen and the growth and development of retinal vessels: In vivo and in vitro studies. Am J Ophthalmol 1966; 62:412–435
Augsburger JJ, Correa ZM, Freire J, Brady LW. Long-term survival in choroidal and ciliary body melanoma after enucleation versus plaque radiation therapy. Ophthalmology. 1998; 105: 1670–1678
Azuara-Blanco A, Dua HS, Pillai CT. Pseudo-endothelial dystrophy associated with emulsified silicone oil. Cornea. 1999; 18:493–494
Balazs EA, Toth LZ, Ozanics V. Cytological studies on the developing vitreous as related to the hyaloid vessel system. Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1980; 213: 71–85
Barbazetto I, Burdan A, Bressler NM, Bressler SB, Haynes L, Kapetanios AD, Lukas J, Olsen K, Potter M, Reaves A, Rosenfeld P, Schachat AP, Strong HA, Wenkenstern A. Treatment of Age-Related Macular Degeneration with Photodynamic Therapy Study Group; Verteporfin in Photodynamic Therapy Study Group. Photodynamic therapy of subfoveal choroidal neovascularization with verteporfin: fluorescein angiographic guidelines for evaluation and treatment — TAP and VIP report No. 2. Arch Ophthalmol. 2003; 121: 1253–1268
Barr CC. The histopathology of successful retinal reattachment. Retina. 1990; 10:189–194
Bartels M. Über die Entstehung von Netzhautablösungen. Klin Monatsbl Augenheilkd 1933; 91: 437–450
Bartz-Schmidt KU, Thumann G, Psichias A, Krieglstein GK, Heimann K. Pars plana vitrectomy, endolaser coagulation of the retina and the ciliary body combined with silicone oil endotamponade in the treatment of uncontrolled neovascular glaucoma. Graefes Arch Clin Exp Ophthalmol. 1999; 237: 969–975
Bartz-Schmidt KU, Kirchhof B, Heimann K. Primary vitrectomy for pseudophakic retinal detachment. Br J Ophthalmol 1996; 80: 346–349
Bechrakis NE, Bornfeld N, Schueler A, Coupland SE, Henze G, Foerster MH. Clinicopathologic features of retinoblastoma after primary chemoreduction. Arch Ophthalmol. 1998; 116: 887–893
Becker MD, Bodaghi B, Holz FG, Harsch N, Hoang PL. Diagnostische Vitrektomie bei Uveitis: Möglichkeiten der Molekularbiologie. Ophthalmologe. 2003; 100: 796–801
Becker MD, Davis J: Vitrectomy in the treatment of uveitis. Am J Ophthalmol, 2005; in press
Becker MD, Harsch N, Zierhut M, Davis JL, Holz FG. Therapeutische Vitrectomie bei Uveitis: Aktueller Stand und Empfehlungen. Ophthalmologe. 2003; 100: 787–795
Bek T. Capillary closure secondary to retinal vein occlusion. A morphological, histopathological, and immunohistochemical study. Acta Ophthalmol Scand. 1998; 76: 643–648
Bek T. Glial cell involvement in vascular occlusion of diabetic retinopathy. Acta Ophthalmol Scand. 1997; 75: 239–243
Bek T. Immunohistochemical characterization of retinal glial cell changes in areas of vascular occlusion secondary to diabetic retinopathy. Acta Ophthalmol Scand. 1997; 75: 388–392
Bellhorn MB, Friedman AH, Wise GN, Henkind P. Ultrastructure and clinicopathologic correlation of idiopathic preretinal macular fibrosis. Am J Ophthalmol 1975; 79: 366–373
Ben-Ezra D, Sahel JA, Harris NL, Hemo I, Albert DM. Uveal lymphoid infiltrates: immunohistochemical evidence for a lymphoid neoplasia. Br J Ophthalmol. 1989; 73: 846–851
Berkowitz BA, Roberts R, Luan H, Peysakhov J, Knoerzer DL, Connor JR, Hohman TC. Drug intervention can correct subnormal retinal oxygenation response in experimental diabetic retinopathy. Invest Ophthalmol Vis Sci. 2005; 46: 2954–2960
Berkowitz BA, Zhang W. Significant reduction of the panretinal oxygenation response after 28% supplemental oxygen recovery in experimental ROP. Invest Ophthalmol Vis Sci. 2000; 41: 1925–1931
Berger AS, Kaplan HJ. Clinical experience with the surgical removal of subfoveal neovascular membranes. Ophthalmology. 1992; 99: 969–975
Beyer NE. Peripheral retinal lesions related to rhegmatogenous retinal detachment. In: Guyer DR, Yannuzzi LA, Chang S, Shields JA, Green WR: Retina Vitreous Macula, WB Saunders, Philadelphia 1999, p 1219–1223
Bidwell AE, Jampol LM, Goldberg MF. Macular holes and excellent visual acuity. Case report. Arch Ophthalmol. 1988; 106: 1350–1351
Binder S, Bonnet M, Velikay M, Gerard JP, Stolba U, Wedrich A and Hohenberg H (1994) Radiation therapy in proliferative vitreoretinopathy. A prospective randomized study. Graefes Arch Clin Exp Ophthalmol 232: 211–214
Blaauwgeers HG, Holtkamp GM, Rutten H, Witmer AN, Koolwijk P, Partanen TA, Alitalo K, Kroon ME, Kijlstra A, van Hinsbergh VW, Schlingemann RO. Polarized vascular endothelial growth factor secretion by human retinal pigment epithelium and localization of vascular endothelial growth factor receptors on the inner choriocapillaris. Evidence for a trophic paracrine relation. Am J Pathol. 1999; 155: 421–428
Blair NP, Liu T, Warren KA, Glaser DA, Kennedy M, Tran H, Larson CA, Atluri P, Saidel MA, Blair MP. Ocular oxygen consumption: estimates using vitreoperfusion in the cat. Retina. 2004; 24: 120–131
Blankenship G, Cortez R, Machemer R: The lens and pars plana vitrectomy for diabetic retinopathy complications, Arch Ophthalmol 1979; 97: 1263–1267
Blankenship GW, Machemer R. Long-term diabetic vitrectomy results: report of 10-year follow-up. Ophthalmology 1985; 92:503–506
Blankenship GW. Preoperative prognostic factors in diabetic pars plana vitrectomy. Ophthalmology 1982; 89:1246–1249
Boldrey EE, Egbert P, Gass JD, Friberg T (1985) The histopathology of familial exudative vitreoretinopathy: a report of two cases. Arch Ophthalmol 103:238–241
Bonnet M. Bielveltz B, Noel et al. Fluorescein angiography after retinal detachment microsurgery. Graefes Arch Clin Exp Ophthalmol 1983; 221: 35–40
Bopp S. Is there room for improvement in pucker surgery? In: Kirchhof B, Wong D (eds.) Essentials in Ophthalmology: Vitreo-retinal surgery. Springer, Heidelberg 2005; p 37–62
Bornfeld N, Talies S, Anastassiou G, Schilling H, Schüler A, Horstmann GA. Endoresektion maligner Melanome der Uvea nach präoperativer stereotaktischer Einzeldosis-Konvergenzbestrahlung mit dem Leksell-Gamma-knife. Ophthalmologe 2002; 99: 338–344
Boulton M, Foreman D, Williams G, McLeod D. VEGF localisation in diabetic retinopathy. Br J Ophthalmol 1998; 82: 561–568
Brazitikos PD. The expanding role of primary pars plana vitrectomy in the treatment of rhegmatogenous noncomplicated retinal detachment. Semin Ophthalmol 2000; 15: 65–77
Brazitikos PD, Androudi S, D’Amico DJ, Papadopoulos N, Dimitrakos SA, Dereklis DL, Alexandridis A, Lake S, Stangos NT. Perfluorocarbon liquid utilization in primary vitrectomy repair of retinal detachment with multiple breaks. Retina 2003; 23: 615–621
Brazitikos PD, D’Amico DJ, Tsinopoulos IT and Stangos NT (1999) Primary vitrectomy with perfluoro-n-octane use in the treatment of pseudophakic retinal detachment with undetected retinal breaks. Retina 19: 103–109
Bringmann A, Reichenbach A. Role of Müller cells in retinal degenerations. Front Biosci. 2001; 6: E72–92
Brockhurst RJ, Albert DM (1981) Pathologic findings in familial exudative vitreoretinopathy. Arch Ophthalmol 99:2134–2146
Bron AJ, Tripathi RC, Tripathi BJ. The inner limiting membrane, Chapter 14, Wolff’s anatomy of the eye, Chapman & Hall 1997; p 488
Brown SM, Jampol LM, Cantrill HL. Intraocular lymphoma presenting as retinal vasculitis. Surv Ophthalmol. 1994; 39: 133–140
Brucker AJ, Michels RG, Green WR. Pars plana vitrectomy in the management of blood-induced glaucoma with vitreous hemorrhage. Ann Ophthalmol 1978; 10: 1427–1437
Bryan JS, Friedman SM, Marnes RN, Margo CE. Experimental vitreous replacement with Perfluorotri-n-Propylamine. Arch Ophthalmol 1994; 112: 1098–1102
Bunin GR, Emanuel BS, Meadows AT, Buckley JD, Woods WG, Hammond GD. Frequency of 13q abnormalities among 203 patients with retinoblastoma. J Natl Cancer Inst. 1989; 81: 370–374
Burk SE, da Mata AP, Snyder ME; Rosa RH, Foster RE. Indocyanine-green assisted peeling of the retinal internal limiting membrane. Ophthalmology 2000; 107: 2010–2014
Byer NE. Long-term natural history of lattice degeneration of the retina. Ophthalmology 1989; 96: 1396–1342
Byer NE. The long-term natural history of senile retinoschisis with implications for management. Ophthalmology 1986; 93: 1127–1137
Byer NE. Cystic retinal tufts and their relationship to retinal detachment. Arch Ophthalmol 1981; 99: 1788–1790
Byer NE. Lattice degeneration of the retina. Surv Ophthalmol 1979; 23: 213
Byer NE. Clinical study of senile retinoschisis. Arch Ophthalmol 1968; 79:36–44
Campochiaro PA, Lim JI. Aminoglycoside toxicity in the treatment of endophthalmitis. The Aminoglycoside Toxicity Study Group. Arch Ophthalmol. 1994 Jan;112(1):48–53.
Campo RV, Sipperley JO, Sneed SR, Park DW, Dugel PU, Jacobsen J, Flindall RJ. Pars plana vitrectomy without scierai buckle for pseudophakic retinal detachments. Ophthalmology 1999; 106:1811–1815
Campochiaro PA, Van Niel E, Vinores SA. Immunocytochemical labeling of cells in cortical vitreous from patients with premacular hole lesions. Arch Ophthalmol 1992; 110: 371–377
Canny CLB, Oliver GL (1976) Fluorescein angiographic findings in familial exudative vitreoretinopathy. Arch Ophthalmol 74:1114–1120
Capeans C, Santos L, Sanchez-Salorio M, Forteza J. Iris metastasis from endometrial carcinoma. Am J Ophthalmol. 1998; 125:729–730
Cardillo JA, Stout JT, LaBree L, Azen SP, Omphroy L, Cui JZ, Kimura H, Hinton DR and Ryan SJ (1997) Post-traumatic proliferative vitreoretinopathy. The epidemiologic profile, onset, risk factors, and visual outcome. Ophthalmology 104: 1166–1173.
Carpineto P, Ciancaglini M, Aharrh-Gnama A, Agnifili L, Cerulli AM, Cirone D, Mastropasqua L. Optical coherence tomography and fundus microperimetry imaging of spontaneous closure of traumatic macular hole: a case report. Eur J Ophthalmol. 2005; 15:165–169
Castro JR, Char DH, Petti PL, Daftari IK, Quivey JM, Singh RP, Blakely EA, Phillips TL. 15 years experience with helium ion radiotherapy for uveal melanoma. Int J Radiat Oncol Biol Phys. 1997; 39: 989–996
Chang A, Zimmerman NJ, Iwamoto T, Ortiz R, Faris D. Experimental vitreous replacement with Perfluorotributylamine. Am J Ophthalmol 1987; 103: 29–37
Chang CJ, Lai WW, Edward DP, Tso MO. Apoptotic photoreceptor cell death after traumatic retinal detachment in humans. Arch Ophthalmol. 1995; 113: 880–886
Chang S, Sparrow JR, Iwamoto T, Gershbein A, Ross R, Ortiz R. Experimental studies of tolerance to intravitreal Perfluoron-octane. Retina 1991; 11: 367–374
Char D, Kaleta-Michaels S, Engman E. Metastatic retinoblastoma. Case report. Arch Ophthalmol. 1989; 107: 1570–1571
Char DH, Ljung BM, Deschenes J, Miller TR. Intraocular lymphoma: immunological and cytological analysis. Br J Ophthalmol. 1988 Dec; 72: 905–911
Char DH, Kroll SM, Castro J. Long-term follow-up after uveal melanoma charged particle therapy. Trans Am Ophthalmol Soc. 1997; 95: 171–187 discussion 187–91
Charles S. Flinn CE: The natural history of diabetic extramacular traction detachment. Arch Ophthalmol 1979; 97: 1268–1272
Chaudhry NA, Lim ES, Saito Y, Mieler WF, Liggett PE, Filatov V: Early vitrectomy and endolaser photocoagulation in patients with type I diabetes with severe vitreous hemorrhage. Ophthalmology 1995; 102: 1164–1169
Cheng L, Azen SP, El-Bradey MH, Scholz BM, Chaidhawangul S, Toyoguchi M, Freeman WR. Duration of vitrectomy and postoperative cataract in the vitrectomy for macular hole study. Am J Ophthalmol. 2001; 132: 881–887
Chuang EL, Bird AC. Repair after tears of the retinal pigment epithelium. Eye. 1988; 2:106–113
Chen YS, Hackett SF, Schoenfeld CL, Vinores MA, Vinores SA, Campochiaro PA. Localisation of vascular endothelial growth factor and its receptors to cells of vascular and avascular epiretinal membranes. Br J Ophthalmol. 1997; 81: 919–926
Cheung MK, Martin DF, Chan CC, Callanan DG, Cowan CL, Nussenblatt RB. Diagnosis of reactive lymphoid hyperplasia by chorioretinal biopsy. Am J Ophthalmol. 1994; 118: 457–462
Chew EY, Benson WE, Remaley NA, Lindley AA, Burton TC, Csaky K, Williams GA, Ferris Fl 3rd (1999) Results after lens extraction in patients with diabetic retinopathy. The Early Treatment Diabetic Retinopathy Study Report number 25. Arch Ophthalmol 117: 1600–1606
Ciulla TA, Pesavento RD, Yoo S. Subretinal aspiration biopsy of ocular lymphoma. Am J Ophthalmol. 1997; 123: 420–422
Clarkson JG, Green WR, Massof D. A histopathologic review of 168 cases of preretinal membrane. Am J Ophthalmol 1977; 84: 1–7
Cockerham GC, Hidayat AA, Bijwaard KE, Sheng ZM. Re-evaluation of “reactive lymphoid hyperplasia of the uvea”: an immunohistochemical and molecular analysis of 10 cases. Ophthalmology. 2000; 107: 151–158
Cogan DG, Kuwabara T. Comparison of retinal and cerebral vasculature in trypsin digest preparations. Br J Ophthalmol 1984;68(1):10–12
Coleman K, Baak JP, Dorman A, Mullaney J, Curran B, Tiernan D, Farrell M, Fenton M, Leader M. Deoxyribonucleic acid ploidy studies in choroidal melanomas. Am J Ophthalmol. 1993; 115:376–383
Collins ET. Unusual changes to the macular region. Trans Ophthalmol Soc UK 1900; 20: 196–197
Condon GP, Brownstein S, Wang NS, Kearns JA, Ewing CC. Congenital hereditary (juvenile X-linked) retinoschisis. Histopathologic and ultrastructural findings in three eyes. Arch Ophthalmol. 1986;104:576–583
Connolly SE, Hores TA, Smith LE, D’Amore PA. Characterization of vascular development in the mouse retina. Microvasc Res 1988; 36: 275–290
Coupland SE, Anastassiou G, Bornfeld N, Hummel M, Stein H. Primary intraocular lymphoma of T-cell type: report of a case and review of the literature. Graefes Arch Clin Exp Ophthalmol. 2005; 243: 189–197
Coupland SE, Hummel M, Müller HH, Stein H. Molecular analysis of immunoglobulin genes in primary intraocular lymphoma. Invest Ophthalmol Vis Sci. 2005; 46: 3507–3514
Coupland SE, Loddenkemper C, Smith JR, Braziel RM, Charlotte F, Anagnostopoulos I, Stein H. Expression of immunoglobulin transcription factors in primary intraocular lymphoma and primary central nervous system lymphoma. Invest Ophthalmol Vis Sci. 2005;46: 3957–3964
Coupland SE, Bechrakis NE, Anastassiou G, Foerster AM, Heiligenhaus A, Pleyer U, Hummel M, Stein H. Evaluation of vitrectomy specimens and chorioretinal biopsies in the diagnosis of primary intraocular lymphoma in patients with Masquerade syndrome. Graefes Arch Clin Exp Ophthalmol. 2003; 241: 860–870
Coupland SE, Foss HD, Hidayat AA, Cockerham GC, Hummel M, Stein H. Extranodal marginal zone B cell lymphomas of the uvea: an analysis of 13 cases. J Pathol. 2002; 197: 333–340
Couvillion SS, Smiddy WE, Flynn HW Jr, Eifrig CW, Gregori G. Outcomes of surgery for idiopathic macular hole: a casecontrol study comparing silicone oil with gas tamponade. Ophthalmic Surg Lasers Imaging. 2005; 36: 365–371
Cramer T, Johnson RS. A novel role for the hypoxia inducible transcription factor HIF-lalpha: critical regulation of inflammatory cell function. Cell Cycle. 2003; 2:192–193
Cramer T, Yamanishi Y, Clausen BE, Forster I, Pawlinski R, Mackman N, Haase VH, Jaenisch R, Corr M, Nizet V, Firestein GS, Gerber HP, Ferrara N, Johnson RS. HIF-lalpha is essential for myeloid cell-mediated inflammation. Cell. 2003; 112:645–657
Criswick VG, Schepens CL (1969) Familial exudative vitreoretinopathy. Am J Ophthalmol 68:578–594
Cursiefen C, Holbach LM, Schlötzer-Schrehardt U, Naumann GOH. Persisting retinal ganglion cell axons in blind atrophie human eyes. Graefe’s Arch Clin Exp. Ophthalmol 2001; 239: 158–164
Da Mata AP, Burk SE, Foster RE, Riemann CD, Petersen MR, Nehemy MB, Augsburger JJ. Long-term follow-up of indocyanine green-assisted peeling of the retinal internal limiting membrane during vitrectomy surgery for idiopathic macular hole repair. Ophthalmology. 2004; 111: 2246–2253
Damato B, Duke C, Coupland SE, Hiscott P, Smith PA, Campbell I, Douglas A, Howard P. Clinical cytogenetics in uveal melanoma: seven years experience. Ophthalmology, 2007 Oct; 114(10): 1925–1931
Damato B, Foulds WS. Indications for trans-scleral local resection of uveal melanoma. Br J Ophthalmol. 1996; 80: 1029–1030
Damato BE, Paul J, Foulds WS. Risk factors for metastatic uveal melanoma after trans-scleral local resection. Br J Ophthalmol. 1996; 80: 109–116
Das T, Biswas J, Kumar A, Nagpal PN, Namperumalsamy P, Patnaik B, Tewari HK. Eales’ disease. Indian J Ophthalmol 1994 Mar;42(1):3–18
Davis JL, Viciana AL, Ruiz P. Diagnosis of intraocular lymphoma by flow cytometry. Am J Ophthalmol. 1997; 124: 362–372
Davids JL, Hummer J, Feuer WJ. Laser photocoagulation for retinal detachments and retinal tears in cytomegalovirus retinitis. Ophthalmology 1997; 104: 2053–2060
Davis MD, Segal PP and McCormick A. The natural course followed by the fellow eye in patients with rhegmatogenous retinal detachment. In: Pruett RC and Regan CDJ (eds): Retinal Congress, New York 1974, Appleton-Century-Crofts, 643–648
de Bustros S. Vitrectomy for prevention of macular holes. Results of a randomized multicenter clinical trial. Vitrectomy for Prevention of Macular Hole Study Group. Ophthalmology. 1994;101:1055–1059
de Bustros S, Thompson JT, Michels RG, Rice TA, Glaser BM. Vitrectomy for idiopathic epiretinal membranes causing macular pucker. Br J Ophthalmol. 1988; 72: 692–695
de Bustros S, Thompson JT, Michels RG, Enger C, Rice TA, Glaser BM. Nuclear sclerosis after vitrectomy for idiopathic epiretinal membranes. Am J Ophthalmol. 1988; 105: 160–164
de Juan E, Lambert HM (1985) Recurrent proliferations in macular pucker, diabetic retinopathy, and retrolental fibroplasias-like disease after vitrectomy. Graefes Arch Clin Exp Ophthalmol 223:174–183
De Luca A, Esposito V, Baldi A, Giordano A. The retinoblastoma gene family and its role in proliferation, differentiation and development. Histol Histopathol. 1996; 11: 1029–1034
Delaney WV Jr, Torrisi PF, Hampton GR, Seigart CR, Hay PB. Hemorrhagic peripheral pigment epithelial disease. Arch Ophthalmol. 1988; 106: 646–650
Desai UR, Strassman IB (1997) Combined pars plana vitrectomy and scierai buckling for pseudophakic and aphakic retinal detachments in which a break is not seen preoperatively. Ophthalmic Surg. Lasers 28:718–722
Devenyi RG, de Carvalho NH. Combined scierai buckle and pars plana vitrectomy as a primary procedure for pseudophakic retinal detachments. Ophthalmic Surg. Lasers 1999; 30:615–618
D’Hermies F, Korobelnik JF. Histological evidence of hydrogel fragmentation. Arch Ophthalmol. 1999; 117: 1449
D’Hermies F, Korobelnik JF, Chauvaud D, Pouliquen Y, Parel JM, Renard G. Scierai and episcleral histological changes related to encircling expiants in 20 eyes. Acta Ophthalmol Scand. 1999; 77: 279–285
Diabetic Retinopathy Vitrectomy Study Research Group. Early vitrectomy for severe vitreous hemorrhage in diabetic retinopathy. Four-year results of a randomized trial: Diabetic Retinopathy Vitrectomy Study Report 5. Arch Ophthalmol. 1990; 108:958–964
Diabetic Retinopathy Vitrectomy Study Research Group. Two-year course of visual acuity in severe proliferative diabetic retinopathy with conventional management. Diabetic Retinopathy Vitrectomy Study (DRVS) report #1. Ophthalmology. 1985; 92: 492–502
Diabetic Retinopathy Vitrectomy Study Research Group. Two-year results of a randomized trial. Diabetic Retinopathy Vitrectomy Study report 2. Arch Ophthalmol. 1985; 103: 1644–1652
Diamond J, Kaplan H. Uveitis: effect of vitrectomy combined with lensectomy. Ophthalmology 1978; 86:1320–1329
Dithmar S, Aabert TM Jr, Grossniklaus HE. Histopathologic changes in retinoblastoma after chemoreduction. Retina. 2000; 20: 33–36
Doi M, Refojo MF. Histopathology of rabbit eyes with intravitreous silicone-fluorosilicone copolymer oil. Exp Eye Res 1994; 59: 737–746
Donders PC. Malignant melanoma of the choroid. Trans Ophthalmol Soc UK 1973;93(0):745–751
Dudgeon J, Lee WR. The trilateral retinoblastoma syndrome. Trans Ophthalmol Soc U K. 1983; 103 (Pt 5): 523–529
Duke Elder S: System of Ophthalmology Vol III, pp 294–308, St Louis: CV Mosby Co 1968
Dumas J and Schepens CL. Chorioretinal lesions predisposing to retinal breaks. Am J Ophthalmol 1966; 61: 620–630
Dunn WJ, Lambert HM, Kincaid MC, Dieckert JP, Shore JW. Choroidal malignant melanoma with early vitreous seeding. Retina. 1988; 8: 188–192
Eaton AM, Jaffe GL, McCuen BW II, Mincey GJ. Condensation on the posterior surface of silicone intraocular lenses during fluid-air exchange. Ophthalmology 1995; 102: 733–736
Eckardt C, Eckardt U, Conrad HJ. Macular rotation with and without counter-rotation of the globe in patients with agerelated macular degeneration. Graefe’s Arch Clin Exp Ophthalmol. 1999; 237: 313–325
Eckardt C. Chirurgische Entfernung von submakulären Neovaskularisationsmembranen. Ophthalmologe. 1996; 93: 688–693
Eckardt C, Nicolai U, Czank M, Schmidt D. Identification of silicone oil in the retina after intravitreal injection. Retina. 1992; 12:S17–22
Eckard C, Nicolai U, Winter M, Knop E. Experimental intraocular tolerance to liquid Perfluorooctane and Perfluoropolyether. Retina 1991; 11:375–384
Eisner G. Autoptische Spaltlampenuntersuchung des Glaskörpers. I-III. Graefes Arch Clin Exp Ophthalmol 1971; 182: 1–40
el-Asrar AM. Primary vitrectomy for bullous rhegmatogenous retinal detachments due to complex breaks. Eur J Ophthalmol. 1997 Oct–Dec; 7(4):322–326
Elavathil LJ, LeRiche J, Rootman J, Gallagher RP, Phillips D. Prognostic value of DNA ploidy as assessed with flow cytometry in uveal melanoma. Can J Ophthalmol. 1995; 30: 360–365
Eller AW, Friberg TR, Mah F. Migration of silicone oil into the brain: a complication of intraocular silicone oil for retinal tamponade. Am J Ophthalmol. 2000; 129: 685–688
Engerman, RL, Meyer, RK. Development of retinal vasculature in rats Am J Ophthalmol 1965; 60: 628–641
Escoffery RF, Olk RJ, Grand MG, Boniuk I. Vitrectomy without scierai buckling for primary rhegmatogenous retinal detachment. Am. J. Ophthalmol. 1985; 99:275–281
Ezra E, Fariss RN, Possin DE, Aylward WG, Gregor ZJ, Luthert PJ, Milam AH. Immunocytochemical characterization of macular hole opercula. Arch Ophthalmol. 2001; 119:223–231
Ezra E, Gregor ZJ; Morfields Macular Hole Study Group Report No. 1. Surgery for idiopathic full-thickness macular hole: two-year results of a randomized clinical trial comparing natural history, vitrectomy, and vitrectomy plus autologous serum: Moorfields Macular Hole Study Group Report no. 1. Arch Ophthalmol. 2004; 122: 224–236
Ezra E, Munro PMG, Charteris DG, et al. Macular hole opercula. Arch Ophthalmol 1997; 115: 1381–1387
Ezra E. Idiopathic full thickness macular hole: natural history and pathogenesis. Br J Ophthalmol. 2001; 85:102–128
Faude F, Reichenbach A, Wiedemann P. Zur Geschichte der Hypothese einer Mitwirkung der Müllerzellen bei der Entwicklung des idiopathischen Makulaforamens. Klin Monatsbl Augenheilkd. 2004; 221: 519–520
Faude F, Francke M, Makarov F, Schuck J, Gartner U, Reichelt W, Wiedemann P, Wolburg H, Reichenbach A. Experimental retinal detachment causes widespread and multilayered degeneration in rabbit retina. J Neurocytol. 2001; 30:379–390
Faulborn J, Ardjomand N. Tractional retinoschisis in proliferative diabetic retinopathy: a histopathological study. Graefes Arch Clin Exp Ophthalmol. 2000; 238: 40–44
Faulborn J, Conway BP, Machemer R. Surgical complications of pars plana vitreous surgery. Ophthalmology, 1978; 85: 116–125
Feron EJ, Veckeneer M, Parys-Van Ginderdeuren R, Van Lommel A, Melles GRJ, Stalmans P. Trypan blue staining of epiretinal membranes in proliferative vitreoretinopathy. Arch Ophthalmol 2002; 120: 141–144
Ferry AP, Font RL. Carcinoma metastatic to the eye and orbit. I. A clinicopathologic study of 227 cases. Arch Ophthalmol. 1974; 92: 276–286
Fineberg E, Machemer R, Sullivan P, Norton EWD, Hamasaki D, Anderson D. Sulfur hexafluoride in owl monkey vitreous cavity. Am J Ophthalmol 1975; 79: 67–76
Finger PT, Berson A, Szechter A. Palladium-103 plaque radiotherapy for choroidal melanoma: results of a 7-year study. Ophthalmology. 1999; 106: 606–613
Finger PT. Radiation therapy for choroidal melanoma. Surv Ophthalmol. 1997; 42:215–232
Flores Aquilar M, Munguia D, Loeb E, Crapotta JA, Vuong C, Shakiba S. Intraocular tolerance of Perfluoro-octylbromide (Perflubrom). Retina 1995; 15: 3–13
Flynn HW Jr, Chew EY, Simons BD, Barton FB, Remaley NA, Ferris FL 3rd. Pars plana vitrectomy in the Early Treatment Diabetic Retinopathy Study. ETDRS report number 17. The Early Treatment Diabetic Retinopathy Study Research Group. Ophthalmology. 1992; 99: 1351–1357
Folberg R, Mehaffey M, Gardner LM, Meyer M, Rummelt V, Pe’er J. The microcirculation of choroidal and ciliary body melanomas. Eye. 1997; 11 (Pt 2): 227–238
Folk JC, Arrindell EL and Klugman NR. The fellow eye of patients with phakic lattice retinal detachment. Ophthalmology 1989; 96: 72–79
Fong DS, Ferris FL 3rd, Davis MD, Chew EY. Causes of severe visual loss in the early treatment diabetic retinopathy study. ETDRS report number 24: Early Treatment Diabetic Retinopathy Study Research Group. Am J Ophthalmol 1999, 127: 137–141
Font RL, Croxatto JO, Rao NA. Armed Forces Institute of Pathology atlas of tumors of the eyes and ocular adnexa. Series 4 ed. Washington: AFIP Press, 2006. Pages 56–59
Font RL, Naumann GOH. Ocular histopathology of pulseless disease. Arch Ophthalmol 1969; 82: 784–788
Foos RY. Ultrastructural features of posterior vitreous detachment. Graefes Arch Clin Exp Ophthalmol 1974; 196:103–111
Foos RY. Vitreous base, retinal tufts and retinal tears: Pathogenic relationships. In: Pruett RC, Regan CDJ (Eds): Retinal Congress. Chapter 20, New York, 1974, Apple-Century-Crofts, Page 259
Foos RY. Post oral peripheral retinal tears. Ann Ophthalmol 1974; 6: 679–689
Foos RY. Vitreoretinal juncture — simple epiretinal membranes. Graefes Arch Clin Exp Ophthalmol 1973; 189: 231–250
Foos RY. Zonular traction tufts of the peripheral retina in cadaver eyes. Arch Ophthalmol 1969; 82: 620–632
Foos RY, Allen RA. Retinal tears and lesser lesions of the peripheral retina in autopsy eyes. Am J Ophthalmol 1967; 64: 643–655
Foulks GN, Hatchell DL, Proia AD, Klintworth GK. Histopathology of silicone oil keratopathy in humans. Cornea. 1991; 10:29–37
Foulds WS, Lee WR, Taylor WO. Clinical and pathological aspects of choroidal ischaemia. Trans Ophthalmol Soc U K. 1971;91:323–341
Frank RN, Amin RH, Eliott D, Puklin JE, Abrams GW. Basic fibroblast growth factor and vascular endothelial growth factor are present in epiretinal and choroidal neovascular membranes. Am J Ophthalmol. 1996; 122: 393–403
Francke M, Faude F, Pannicke T, Uckermann O, Weick M, Wolburg H, Wiedemann P, Reichenbach A, Uhlmann S, Bringmann A. Glial cell-mediated spread of retinal degeneration during detachment: a hypothesis based upon studies in rabbits. Vision Res. 2005; 45: 2256–2267
Fraser-Bell S, Guzowski M, Rotchina E, Wang JJ, Mitchell P. Five-year cumulative incidence and progression of epiretinal membranes. The Blue Mountains Eye Study. Ophthalmology 2003; 110:34–40
Freeman WR, Azen SP, Kim JW, el-Haig W, Mishell DR 3rd, Bailey I. Vitrectomy for the treatment of full-thickness stage 3 or 4 macular holes. Results of a multicentered randomized clinical trial The Vitrectomy for Treatment of Macular Hole Study Group. Arch Ophthalmol. 1997; 115: 11–21
Freeman WR. Vitrectomy surgery for full-thickness macular holes. Am J Ophthalmol. 1993; 116: 233–235
Fruttiger M. Development of the mouse retinal vasculature: angiogenesis versus vasculogenesis. Invest Ophthalmol Vis Sci. 2002; 43: 522–557
Furino C, Micelli Ferrari T, Boscia F, Cardascia N, Recchimurzo N, Sborgia C. Triamcinolone-assisted pars plana vitrectomy for proliferative vitreoretinopathy. Retina 2003; 23: 771–776
Gabbiani G and Badonnel MC (1976) Contractile events during inflammation. Agents Actions 6: 277–280
Gallie BL, Budning A, DeBoer G, Thiessen JJ, Koren G, Verjee Z, Ling V, Chan HS. Chemotherapy with focal therapy can cure intraocular retinoblastoma without radiotherapy. Arch Ophthalmol. 1996; 114: 1321–1328
Gandorfer A, Rohleder M, Grosselfinger S, Haritoglou C, Ulbig M, Kampik A. Epiretinal pathology of diffuse diabetic macular edema associated with vitreomacular traction. Am J Ophthalmol. 2005; 139: 638–652
Gariano RF, Iruela-Arispe ML, Sage EH, Hendrickson AE. Immunohistochemical characterization of developing and mature primate retinal blood vessels. Invest Ophthalmol Vis Sci. 1996; 37: 93–103.
Gariano RF, Sage EH, Kaplan HJ, Hendrickson AE. Development of astrocytes and their relation to blood vessels in fetal monkey retina. Invest Ophthalmol Vis Sci. 1996; 37: 2367–2375
Gartry DS, Chignell AH, Franks WA, Wong D. Pars plana vitrectomy for the treatment of rhegmatogenous retinal detachment uncomplicated by advanced proliferative vitreoretinopathy. Br J Ophthalmol 1993; 77: 199–203
Gass JDM. Bullous retinal detachment. An unusual manifestation of idiopathic central serous choroidopathy. Am J Ophthalmol 1973; 75(5):810–821
Gass JDM. Muller cell cone, an overlooked part of the anatomy of the fovea centralis. Hypotheses concerning its role in the pathogenesis of macular hole and foveomacular retinoschisis. Arch Ophthalmol 1999; 117: 821–823
Gass JDM. Reappraisal of biomicroscopic classification of stages of development of a macular hole. Am J Ophthalmol 1995; 119:752–759
Gass JD. Biomicroscopic and histopathologic considerations regarding the feasibility of surgical excision of subfoveal neovascular membranes. Am J Ophthalmol. 1994; 118: 285–298
Gass JDM. Idiopathic senile macular hole: its early stages and development. Arch Ophthalmol 1988; 106: 629–639
Gastaud P, Rouhette H, Negre F, Leguay JM, Dorafourg F. Place de la “vitrectomie exploratrice” dans le traitement du décollement de rétine sans prolifération vitréo-rétinienne. J Fr Ophtalmol 2000; 23: 482–487
George ND, Yates JR, Moore AT. Clinical features in affected males with X-linked retinoschisis. Arch Ophthalmol. 1996; 114:274–280
Gibran SK, Alwitry A, Cleary PE. Foveal detachment after successful retinal reattachment for macula on rhegmatogeneous retinal detachment: an ocular coherence tomography evaluation. Eye. 2005 Sep 30
Gieser AS, Murphy RP: Eales disease. Retina 1994; 2: 1503–1507
Girard P, Karpouzas I. Vitrectomie dans le traitement du décollement de retine simplement. J Fr Ophtalmol 1995; 18:188–193
Glazer LC, Maguire A, Blumenkranz MS, Trese MT, Green WR. Improved surgical treatment of familial exudative vitreoretinopathy in children. Am J Ophthalmol 1995; 120:471–479
Glaser BM, Michels RG, Kupperman BD, Sjaarda RN, Pena RA. The effects of pars plana vitrectomy and transforming growth factor-beta 2 for the treatment of full-thickness macular holes: a prospective randomized study. Ophthalmology 1992; 99: 1162–1173
Gloor B. Zur Entwicklung des Glaskörpers und der Zonula. V. Zur Entwicklung der Netzhautgefäße des Kaninchens. von Graefes Arch Clin Exp Ophthalmol 1973; 187: 147
Gloor B.P. Zur Entwicklung des Glaskörpers und der Zonula. I. Überblick und chronologischer Ablauf der Glaskörper-und Zonulaentwicklung bei Kaninchen und Maus. Graefes Arch Clin Exp Ophthalmol 1973; 186: 299
Goldberg ME Retinal vaso-occlusion in sickling hemoglobinopathies. Birth Defects Orig Artic Ser 1976; 12(3):475–515. Review
Gonin J. Pathogenie et anatomie pathologique des decollemends retiniens. Bull Mem Soc d’Ophtalmol 1920; 33:1–8
Gow J, Oliver GL (1971) Familial exudative vitreoretinopathy: an expanded view. Arch Ophthalmol 86:150–155
Gragoudas ES, Seddon JM, Egan K, Glynn R, Munzenrider J, Austin-Seymour M, Goitein M, Verhey L, Urie M, Koehler A. Long-term results of proton beam irradiated uveal melanomas. Ophthalmology. 1987; 94: 349–353
Green RL, Byrne SF. Diagnostic ophthalmic ultrasound. Ryan SJ, et. Retina, et 2, St. Louis, 1994; Mosby
Grossniklaus HE, Martin DF, Avery R, Shields JA, Shields CL, Kuo IC, Green RL, Rao NA. Uveal lymphoid infiltration. Report of four cases and clinicopathologic review. Ophthalmology. 1998; 105(7): 1265–1273
Grossniklaus HE, Gass JD. Clinicopathologic correlations of surgically excised type 1 and type 2 submacular choroidal neovascular membranes. Am J Ophthalmol. 1998; 126: 59–69
Grossniklaus HE, Albert DM, Green WR, Conway BP, Hovland KR. Clear cell differentiation in choroidal melanoma. COMS report no. 8. Collaborative Ocular Melanoma Study Group. Arch Ophthalmol. 1997; 115: 894–898
Gun duz K, Shields JA, Shields CL, Eagle RC Jr, Diniz W, Mercado G, Chang W. Transscleral choroidal biopsy in the diagnosis of choroidal lymphoma. Surv Ophthalmol. 1999; 43: 551–555
Guyer DR, Green WR, de Bustros S, Fine SL. Histopathologic features of idiopathic macular holes and cysts. 1990. Retina. 2005; 25: 1045–1051
Guyer DR, Green WR, Schachat AP, Bastacky S, Miller NR. Bilateral ischemic optic neuropathy and retinal vascular occlusions associated with lymphoma and sepsis. Clinicopathologic correlation. Ophthalmology. 1990; 97: 882–888
Guyer DR, Green WR, de Bustros S, Fine SL. Histopathologic features of idiopathic macular holes and cysts. Ophthalmology. 1990; 97: 1045–1051
Hadden PW, Hiscott PS, Damato BE. Histopathology of eyes enucleated after endoresection of choroidal melanoma. Ophthalmology. 2004; 111: 154–160
Haimann MH, Burton TC, Brown CK. Epidemiology of retinal detachment. Arch Ophthalmol 1982; 100: 289–292
Hagimura N, Iida T, Suto K, Kishi S. Persistent foveal retinal detachment after successful rhegmatogenous retinal detachment surgery. Am J Ophthalmol. 2002; 133: 516–520
Hakin KN, Lavin MJ, Laever PK. Primary vitrectomy for rhegmatogenous retinal detachment. Graefes Arch Clin Exp Ophthalmol 1993; 231: 344–346
Halfter W, Dong S, Schurer B, Ring C, Cole GJ, Eller A. Embryonic synthesis of the inner limiting membrane and vitreous body. Invest Ophthalmol Vis Sci. 2005; 46: 2202–2209
Halfter W, Willem M, Mayer U. Basement membrane-dependent survival of retinal ganglion cells. Invest Ophthalmol Vis Sci 2005; 46: 1000–1009
Halfter W Disruption of the retinal basal lamina during early embryonic development leads to a retraction of vitreal endfeet, and increased number of ganglion cells, and aberrant axon outgrowth. J Comp Neurol 1998; 397: 89–104
Haritoglou C, Gandorfer A, Gass CA, Kampik A. Histology of the vitreoretinal interface after staining of the internal limiting membrane using 5% diluted indocyanine and infracyanine green. Am J Ophthalmol 2004; 137: 345–348
Haritoglou C, Gandorfer A, Gass CA, Schaumberger M, Ulbig MW, Kampik A. Indocyanine green-assisted peeling of the internal limiting membrane in macular hole surgery affects visual outcome: a clinicopathologic correlation. Am J Ophthalmol. 2002; 134: 836–841
Heiligenhaus A, Bornfeld N, Wessing A. Longterm results of pars plana vitrectomy in the management of intermediate uveitis. Curr Opin Ophthalmol 1996; 7:77–79
Helbig H: Diabetische Traktionsablatio. Klin Monatsbl Augenheilkd 2002; 219: 186–190
Helbig H, Kellner U, Bornfeld N, Foerster MH: Vitrektomie bei diabetischer Retinopathie: Ergebnisse, Risikofaktoren, Komplikationen. Klin Monatsbl Augenheilkd 1998; 212: 339–342
Helbig H, Kellner U, Bornfeld N, Foerster MH: Rubeosis iridis after vitrectomy for diabetic retinopathy. Graefes Arch Clin Exp Ophthalmol 1998; 236: 730–733
Helbig H, Kellner U, Bornfeld N, Foerster MH: Grenzen und Möglichkeiten der Glaskörperchirurgie bei diabetischer Retinopathie 1996; 93: 647–654
Heimann H, Bornfeld N, Friedrichs W, Helbig H, Kellner U, Korra A, Foerster MH. Primary vitrectomy without scierai buckling for rhegmatogenous retinal detachment. Graefes Arch Clin Exp Ophthalmol 1996; 234: 561–568
Heimann H, Hellmich M, Bornfeld N, Bartz-Schmidt KU, Hilgers RD, Foerster MH. Scierai buckling versus primary vitrectomy in rhegmatogenous retinal detachment (SPR Study): design issues and implications. SPR Study report no. 1. Graefes Arch Clin Exp Ophthalmol 2001; 239:567–574
Hirata F, Yoshida M, Ogura Y. High glucose exacerbates neutrophil adhesion to human retinal endothelial cells. Exp Eye Res. 2005 Sep 29 online
Hirayama K, Hata Y, Noda Y, Miura M, Yamanaka I, Shimokawa H, Ishibashi T. The involvement of the rho-kinase pathway and its regulation in cytokine-induced collagen gel contraction by hyalocytes. Invest Ophthalmol Vis Sci. 2004; 45: 3896–3903
Hiscott P. Macrophages in the pathobiology of epiretinal membranes: multifunctional cells for a multistage process. Br J Ophthalmol 1993;77: 686–687
Ho AC, Guyer DR, Fine SL. Macular hole. Surv Ophthalmol. 1998;42:393–416
Ho T, Smiddy WE, Flynn HWJ: Vitrectomy in the management of diabetic eye disease. Surv Ophthalmol 1992; 37:190–202
Hoerauf H, Müller M, Laqua H. Mouches volantes und Vitrektomie bei vollem Visus? Ophthalmologe. 2003; 100:639–643
Hoerauf H, Roider J, Herboth T, Hager A, Laqua H. Ergebnisse der Vitrektomie bei rhegmatogener Amotio und dichten Glaskörpertrübungen. Klin. Monatsbl. Augenheilkd. 1997; 211:369–374
Hofman P, van Blijswijk BC, Gaillard PJ, Vrensen GF, Schlingemann RO. Endothelial cell hypertrophy induced by vascular endothelial growth factor in the retina: new insights into the pathogenesis of capillary nonperfusion. Arch Ophthalmol. 2001; 119:861–866
Hogan MJ, Alvarado JA, Weddell JE. Histology of the human eye. An atlas and textbook. Philadelphia: WB Saunders, 1971; 492–497
Hogan MJ, Alvarado JA, Weddell JE (eds): Histology of the human eye. Philadelphia: WB Saunders, CA; 1971, p 607–637
Hogan MJ, Alvarado JA, Weddell J.E. Retina. In: Histology of the Human Eye, WB. Saunders Company 1971, pp. 393–522
Hoing C, Heidenkummer HP and Kampik A. Primäre Vitrektomie bei der rhegmatogenen Netzhautablösung. Ophthalmologe 1995; 92:668–671
Hoing C, Kampik A, Heidenkummer HP. Pars plana Vitrektomie mit intraokularer SF6 Tamponade bei komplizierter Netzhautablösung. Ophthalmologe 1994; 91:312–318
Hollenberg MJ, Spira AW. Human retinal development: ultrastructure of the outer retina. Am J Anat. 1973; 137:357–385
Holey GP, Alam A, Kiri A, Edelhauser HF. Effect of indocyanine green intraocular stain on human and rabbit corneal endothelial structure and viability. An in vitro study. J Cat Refr Surg 2002;28: 1027–1033
Hope-Ross M, Yannuzzi LA, Gragoudas ES, Guyer DR, Slakter JS, Sorenson JA, Krupsky S, Orlock DA, Puliafito CA. Adverse reactions due to indocyanine green. Ophthalmology. 1994; 101:529–533
Horiguchi M, Miyake K, Ohta IN, Ito Y. Staining of the lens capsule for circular continuous capsulorrhexis in eyes with white cataracts. Arch Ophthalmol 1998; 116: 535–537
Hovlang KR. Vitreous findings in fellow eyes of aphakic retinal detachment. Am J Ophthalmol 1978; 86: 350–353
Hudson HL, Frambach DA, Lopez PF. Relation of the functional and structural fundus changes after submacular surgery for neovascular age-related macular degeneration. Br J Ophthalmol. 1995; 79: 417–423
Hughes S, Yang H, Chan-Ling T. Vascularization of the human fetal retina: roles of vasculogenesis and angiogenesis. Invest Ophthalmol Vis Sci 2000; 41: 1217–1228
Hui YN, Goodnight R, Zhang XJ, Sorgente N, Ryan SJ. Glial epiretinal membranes and contraction. Immunohistochemical and morphological studies. Arch Ophthalmol. 1988; 106: 1280–1285
Hung JY, Hilton GF. Neovascular glaucoma in a patient with X-linked juvenile retinoschisis. Ann Ophthalmol. 1980; 12: 1054–1055
Hutton WL, Pesicka GA, Fuller DG. Cataract extraction in the diabetic eye after vitrectomy. Am J Ophthalmol 1987; 104: 1–4
Imperia PS, Lazarus HM, Lass JH. Ocular complications of systemic cancer chemotherapy. Surv Ophthalmol. 1989; 34: 209–230
Ishida S, Yamazaki K, Shinoda K, Kawashima S, Oguchi Y. Macular hole retinal detachment in highly myopic eyes: ultrastructure of surgically removed epiretinal membrane and clinicopathologic correlation. Retina. 2000; 20: 176–183
Ito Y, Berkowitz BA. MR studies of retinal oxygenation. Vision Res. 2001; 41: 1307–1311
Jaffe ES, Sander CA, Flaig MJ. Cutaneous lymphomas: a proposal for a unified approach to classification using the R.E.A.L./WHO Classification. Ann Oncol. 2000; 11: 17–21
Jakobiec FA, Sacks E, Kronish JW, Weiss T, Smith M. Multifocal static creamy choroidal infiltrates. An early sign of lymphoid neoplasia. Ophthalmology. 1987; 94: 397–406
James M, Fenman SS. Macular holes. Graefes Arch Klin Exp Ophthalmol 1980; 215: 59–63
Jampol LM, Moy CS, Murray TG, Reynolds SM, Albert DM, Schachat AP, Diddie KR, Engstrom RE Jr, Finger PT, Hovland KR, Joffe L, Olsen KR, Wells CG; Collaborative Ocular Melanoma Study Group (COMS Group). The COMS randomized trial of iodine 125 brachytherapy for choroidal melanoma: IV. Local treatment failure and enucleation in the first 5 years after brachytherapy. COMS report no. 19. Ophthalmology. 2002;109: 2197–2206
Jensen OA. Malignant melanomas of the human uvea: 25-year follow-up of cases in Denmark, 1943—1952. Acta Ophthalmol (Copenh). 1982; 60: 161–182
Jiang B, Bezhadian MA, Caldwell RB. Astrocytes modulate retinal vasculogenesis: effects on endothelial cell differentiation Glia 1995; 15: 1–10
Johnson RN, Gass JDM. Idiopathic macular holes. Observations, stages of formation and implications for surgical intervention. Ophthalmology 1988; 95: 917–924
Jonas JB, Schneider U, Naumann GOH. Count and density of human retinal photoreceptors. Graefes Archiv Clin Exp Ophthalmol 1992; 230: 505–519
Joussen AM, Heussen FMA, Joeres S, Llacer H, Prinz B, Rohrschneider K, Maaijwee KJM, van Meurs J, Kirchhof B. Autologous translocation of the choroid and RPE in age related macular degeneration. Am J Ophthalmol 2006; Jul;142(1):17–30
Joussen AM, Poulaki V, Le ML, Koizumi K, Esser C, Janicki H, Schraermeyer U, Kociok N, Fauser S, Kirchhof B, Kern TS, Adamis AP. A central role for inflammation in the pathogenesis of diabetic retinopathy. FASEB J. 2004; 18: 1450–1452
Joussen AM, Poulaki V, Mitsiades N, Cai WY, Suzuma I, Pak J, Ju ST, Rook SL, Esser P, Mitsiades CS, Kirchhof B, Adamis AP, Aiello LP. Suppression of Fas-FasL-induced endothelial cell apoptosis prevents diabetic blood-retinal barrier breakdown in a model of streptozotocin-induced diabetes. FASEB J. 2003; 17:76–78
Joussen AM, Walter P, Jonescu-Cuypers CP, Koizumi K, Poulaki V, Bartz-Schmidt KU, Krieglstein GK and Kirchhof B (2003) Retinectomy for treatment of intractable glaucoma: long term results. Br J Ophthalmol 87: 1094–1102
Joussen AM, Poulaki V, Qin W, Kirchhof B, Mitsiades N, Wiegand SJ, Rudge J, Yancopoulos GD, Adamis AP. Retinal vascular endothelial growth factor induces intercellular adhesion molecule-1 and endothelial nitric oxide synthase expression and initiates early diabetic retinal leukocyte adhesion in vivo. Am J Pathol 2002; 160: 501–509
Joussen AM, Murata T, Tsujikawa A, Kirchhof B, Burseil SE, Adamis AP. Leukocyte-mediated endothelial cell injury and death in the diabetic retina. Am J Pathol. 2001; 158:147–152
Joussen AM, Joeres S, Fawzy N, Heussen FM, Llacer H, van Meurs JC, Kirchhof B. Autologous translocation of the choroid and retinal pigment epithelium in patients with geographic atrophy. Ophthalmology. 2007 Mar;114(3):551–560
Jurklies B, Anastassiou G, Ortmans S, Schüler A, Schilling H, Schmidt-Erfurth U, Bornfeld N. Photodynamic therapy using verteporfin in circumscribed choroidal haemangioma. Br J Ophthalmol. 2003; 87: 84–89
Kadonoso K, Itoh N, Uchio E, Makamura S, Ohno S. Staining of internal limiting membrane in macular hole surgery. Arch Ophthalmol 2000; 118: 1116–1118
Karel I, Michalickova M and Kuthan P (1997) [Long-term results of pars plana vitrectomy and silicone oil in large retinal tears in children]. Cesk Slov Oftalmol 53: 147–154
Kelly NE, Wendel RT. Vitreous surgery for idiopathic macular holes: results of a pilot study. Arch Ophthalmol 1991; 190: 654–659
Khalil MK. Balloon cell malignant melanoma of the choroid: ultrastructural studies. Br J Ophthalmol. 1983; 67: 579–584
Khawly JA, Lambert RJ, Jaffe GJ. Intraocular lens changes after short-and long-term exposure to intraocular silicone oil. An in vivo study. Ophthalmology. 1998; 105: 1227–1233
Kim JW, Freeman WR, Azen SP, el-Haig W, Klein DJ, Bailey IL. Prospective randomized trial of vitrectomy or observation for stage 2 macular holes. Vitrectomy for Macular Hole Study Group. Am J Ophthalmol. 1996; 121:605–614
Kimura H, Kuroda S, Nagata M. Triamcinolone acetonide-assisted peeling of the internal limiting membrane. Am J Ophthalmol 2004; 137: 172–173
Kindy-Degnan NA, Char DH, Castro JR, Kroll S, Stone RD, Quivey JM, Phillips TL, Irvine AR. Effect of various doses of radiation for uveal melanoma on regression, visual acuity, complications, and survival. Am J Ophthalmol. 1989; 107: 114–120
Kirchhof B, Tavakolian U, Paulmann H, Heimann K. Histopathological findings in eyes after silicone oil injection. Graefes Arch Clin Exp Ophthalmol. 1986; 224: 34–37
Kishi S, Shimizi K: Posterior precortical vitreous pocket. Arch Ophthalmol 1990; 108: 979–982
Kivela T. Trilateral retinoblastoma: a meta-analysis of hereditary retinoblastoma associated with primary ectopic intracranial retinoblastoma. J Clin Oncol. 1999; 17(6): 1829–1837
Klöti R. Amotio-Chirurgie ohne Skleraeindellung. Primäre Vitrektomie. Klin Monatsbl Augenheilkd 1983; 182, 474–478
Knorr HL, Seltsam A, Holbach L, Naumann GO. [Intraocular silicone oil tamponade. A clinico-pathologic study of 36 enucleated eyes]. Ophthalmologe. 1996 Apr;93(2):130–138
Kociok N, Gavranic C, Kirchhof B, Joussen AM. Influence on membrane-mediated cell activation by vesicles of silicone oil or perfluorohexyloctane. Graefes Arch Clin Exp Ophthalmol. 2005; 243: 345–358
Kohno T, Sorgente N, Ishibashi T, Goodnight R, Ryan SJ. Immunofluorescent studies of fibronectin and laminin in the human eye. Invest Ophthalmol Vis Sci. 1987; 28: 506–514
Kokame GT, de Bustros S, The Vitrectomy for Prevention of Macular Hole Study Group. Visual acuity as a prognostic indicator in stage 1 macular holes. Am J Ophthalmol 1995; 119: 112–114
Koniszewski G, Lang GK, Naumann GOH, Knorr HLJ. Prophylaktische YAG-Iridotomie zur Vermeidung des sekundären Winkelblock-Glaukoms nach Pars-Plana-Vitrektomie und Silikon in phaken Augen. Fortschr Ophthalmol 1988; 85: 462–463
Küchle M, Nguyen NX, Naumann GOH. Aqueous flare in eyes with choroidal malignant melanoma. Am J Ophthalmol 1992; 113:207–208
Kurihara T, Noda K, Ishida S, Inoue M. Pars plana vitrectomy with internal limiting membrane removal for macular hole associated with proliferative diabetic retinopathy. Graefes Arch Clin Exp Ophthalmol. 2005; 243: 724–726
Kwok AK, Lai TY, Yuen KS, Tarn BS, Wong VW Macular hole surgery with or without in docyanine green stained internal limiting membrane peeling. Clin Exp Ophthalmol 2003; 31: 470–475
Lafaut BA, Aisenbrey S, Van den Broecke C, Bartz-Schmidt KU, Heimann K. Polypoidal choroidal vasculopathy pattern in age-related macular degeneration: a clinicopathologic correlation. Retina. 2000; 20: 650–654
La Heij EC, Tecim S, Kessels AG, Liem AT, Japing WJ, Hendrikse F: Clinical variables and their relation to visual outcome after vitrectomy in eyes with diabetic retinal traction detachment. Graefes Arch Clin Exp Ophthalmol 2004; 242(3): 210–217.
Lai JC, Stinnett SS, McCuen BW. Comparison of silicone oil versus gas tamponade in the treatment of idiopathic fullthickness macular hole. Ophthalmology. 2003; 110: 1170–1174
Lambert HM, Capone AJ, Aaberg TM, Strenberg PJ, Mandell BA, Lopez PF. Surgical excision of subfoveal neovascular membranes in age-related macular degeneration. Am J Ophthalmol. 1992; 113: 257–262
Lang GE: Differential diagnosis vitreoretin. Klin Monatsbl Augenheilkde 1990
Lang GK, FJ Daumann: The Peripheral Retina and Choroid in Healthy Eyes (3125 Airplane Pilots). Klin. Mbl. Augenheilk. 181 (1982) 493–495
Lang GE, B Laudi, RA Pfeiffer: Autosomal dominant vitreoretinal dystrophy with skeletal dysplasia in one generation. Klin. Mbl. Augenhk. 198 (1991) 207–214
Lang GE, Lang GK, Naumann GOH. Akzidenteile bilaterale asymmetrische Rubin-Laser-Makulopathie. Klin Monatsbl Augenheilkd 1985; 186:366–370
Lang GE, Maumanee I. KMO Lang Glaskörper, Daumann FJ. Periphere Fundusveränderungen bei “Augengesunden” (Piloten). Klin Monatsbl Augenheilkd 1982; 181:493–495
Lansing MB, Glaser BM, Liss H, et al. The effect of pars plana vitrectomy and transforming growth factor-beta 2 without epiretinal membrane peeling on full-thickness macular holes. Ophthalmology 1993; 100: 868–871
Lappas A, Foerster AM, Weinberger AW, Coburger S, Schräge NF, Kirchhof B. Translocation of iris pigment epithelium in patients with exudative age-related macular degeneration: long-term results. Graefes Arch Clin Exp Ophthalmol. 2004; 242:638–647
Lappas A, Weinberger AWA, Foerster AMH, Kube Th, Kirchhof B. Iris pigment epithelium translocation in age related macular degeneration, Graefes Arch Exp Clin Ophthalmol. 2000; 238:631–641
Laqua H (1980) Familial exudative vitreoretinopathy. Graefes Arch Clin Exp Ophthalmol 213:121–133
Lee WR (Ed.), Ophthalmic histopathology, Chapter 7: Treatment of retinal detachment, Springer Heidelberg 2002; p 217–235
Lemor M, Yeo JH and Glaser BM (1986) Oral colchicine for the treatment of experimental traction retinal detachment. Arch Ophthalmol 104: 1226–1229
Lewis GP, Fisher SK. Müller cell outgrowth after retinal detachment: association with cone photoreceptors. Invest Ophthalmol Vis Sci. 2000; 41(6): 1542–1545
Lewis GP, Matsumoto B, Fisher SK. Changes in the organization and expression of cytoskeletal proteins during retinal degeneration induced by retinal detachment. Invest Ophthalmol Vis Sci. 1995; 36: 2404–2416
Lewis H. Peripheral retinal degenerations and the risk of retinal detachment. Am J Ophthalmol. 2003; 136: 155–160
Lewis H, Cowan GM, Straatsma BR. Apparent disappearance of a macular hole associated with development of an epiretinal membrane. Am J Ophthalmol. 1986; 102: 172–175
Li K, Wong D, Hiscott P, Stanga P, Groenwald C, McGalliard J. Trypan blue staining of the internal limiting membrane and epiretinal membrane during vitrectomy: visual results and histopathological findings. Br J Ophthalmol 2003; 87: 216–219
Ling TL, Mitrofanis J, Stone J. Origin of retinal astrocytes in the rat: evidence of migration from the optic nerve J Comp Neurol 1989; 286: 345–352
Loeffler KU, Lee WR. Terminology of sub-RPE deposits: do we all speak the same language? Br J Ophthalmol. 1998; 82: 1104–1105
Logani S, Cho AS, Ali BH, Withers HR, McBride WH, Kozlov KL, Hall MO, Lee DA, Straatsma BR. Single-dose compared with fractionated-dose radiation of the OM431 choroidal melanoma cell line. Am J Ophthalmol. 1995; 120: 506–510
Lohmann DR, Gallie BL. Retinoblastoma: revisiting the model prototype of inherited cancer. Am J Med Genet C Semin Med Genet. 2004 Aug 15;129(1):23–28. Review
Lommatzsch PK. Results after beta-irradiation (106Ru/106Rh) of choroidal melanomas: 20 years experience. Br J Ophthalmol 1986; 70: 844–851
Longaker MT, Chiu ES, Harrison MR, Crombleholme TM, Langer JC, Duncan BW, Adzick NS, Verrier ED and Stern R (1989) Studies in fetal wound healing. IV. Hyaluronic acidstimulating activity distinguishes fetal wound fluid from adult wound fluid. Ann Surg 210: 667–672
Luke C, Luke M, Dietlein TS, Hueber A, Jordan J, Sickel W, Kirchhof B. Retinal tolerance to dyes. Br J Ophthalmol. 2005; 89: 1188–1191
Luthert PJ, Chong NH. Photoreceptor rescue. Eye 1998; 12: 591–596
Machemer R, Sugita G and Tano Y. Treatment of intraocular proliferations with intravitreal steroids. Trans Am Ophthalmol 1979; Soc 77: 171–180
Machemer R (1968) Experimental retinal detachment in the owl monkey. II. Histology of retina and pigment epithelium. Am J Ophthalmol 66: 396–410.
Machemer R. Experimental retinal detachment in the owl monkey. IV. The reattached retina. Am J Ophthalmol 1968; 66: 1075–1091
Madreperla SA, McCuen BW II, Hickingbotham D, et al. Clinicopathologic correlation of surgically removed macular hole opercula. Am J Ophthalmol 1995; 120: 197–207
Mäkitie T, Summanen P, Tarkkanen A, Kivelä T. Microvascular density in predicting survival of patients with choroidal and ciliary body melanoma. Invest Ophthalmol Vis Sci 1999; 40:2471–2480
Mäkitie T, Summanen P, Tarkkanen A, Kivelä T. Microvascular loops and networks as prognostic indicators in choroidal and ciliary body melanomas. J Natl Cancer Inst 1999; 91:359–367
Mäkitie T, Summanen P, Tarkkanen A, Kivelä T. Tumor-infiltrating macrophages (CD68(+) cells) and prognosis in malignant uveal melanoma. Invest Ophthalmol Vis Sci 2001; 42:1414–1421
Manschot WA, Van Peperzeel HA. Uveal melanoma: location, size, cell type, and enucleation as risk factors in metastasis. Hum Pathol. 1982; 13: 1147–1148
Marcus DM, Craft JL, Albert DM. Histopathologic verification of Verhoeff’s 1918 irradiation cure of retinoblastoma. Ophthalmology. 1990; 97: 221–224
Margherio RR, Cox MS Jr, Trese MT, Murphy PL, Johnson J, Minor LA. Removal of epimacular membranes. Ophthalmology. 1985; 92: 1075–1083
Marmor MF. Control of subretinal fluid: experimental and clinical studies. Eye. 1990; 4 (Pt 2): 340–344
Martegiani F: Novae Observationes de oculo humano, Neapoli: Typis Cajetani Eboli 1814; pp 16–24
Martin DF, Chan CC, de Smet MD, Palestine AG, Davis JL, Whitcup SM, Burnier MN Jr, Nussenblatt RB. The role of chorioretinal biopsy in the management of posterior uveitis. Ophthalmology. 1993;100: 705–714
Matsumura N, Ikuno Y, Tano Y. Posterior vitreous detachment and macular hole formation in myopic foveoschisis. Am J Ophthalmol. 2004; 138: 1071–1073
Mazzuca DE, Benson WE. Central serous retinopathy: variants. Surv Ophthalmol. 1986; 31:170–174
McDermott HR, Puklin JE, Abrams GW, Eliott D: Phacoemulsification for cataract following pars plana vitrectomy. Ophthalmic Surg Lasers 1997; 28: 558–564
McDonnell PJ, Fine SL, Hillis AI. Clinical features of idiopathic macular cysts and holes. Am J Ophthalmol 1982; 93:777–786
McLean IW, Foster WD, Zimmerman LE. Uveal melanoma: location, size, cell type, and enucleation as risk factors in metastasis. Hum Pathol. 1982; 13: 123–132
McLean IW, Foster WD, Zimmerman LE, Gamel JW. Modifications of Callender’s classification of uveal melanoma of the Armed Forces Institute of Pathology. Am J Ophthalmol 1983; 96:502–509
McLean IW, Keefe KS, Burnier MN. Uveal melanoma. Comparison of the prognostic value of fibrovascular loops, mean of the ten largest nucleoli, cell type, and tumor size. Ophthalmology. 1997; 104: 777–780
McLean IW, Zimmerman LE, Evans RM. Reappraisal of Callender’s spindle a type of malignant melanoma of choroid and ciliary body. Am J Ophthalmol 1978; 86:557–564
McLeod DS, Merges C, Fukushima A, Goldberg MF, Lutty GA. Histopathologic features of neovascularization in sickle cell retinopathy. Am J Ophthalmol. 1997 Oct; 124: 455–472
McPherson A, O’Malley R and Beltangady SS. Management of the fellow eyes of patients with rhegmatogenous retinal detachment. Ophthalmology 1981; 88: 922–934
McPherson A. (ed.) “New and Controversial Aspects of Retinal Detachment”, Hoeber Pub. New York, 1968
Meinert H, Knoblich A. The use of semifluorinated alkanes in blood-substitutes. Biomater Artif Cells Immobilization Biotechnol. 1993; 21: 583–595
Meredith JE Jr, Fazeli B, Schwartz MA. The extracellular matrix as a cell survival factor. Mol Biol Cell 1993; 4: 953–961
Messmer EM, Heidenkummer HP, Kampik A. Ultrastructure of epiretinal membranes associated with macular holes. Graefes Arch Clin Exp Ophthalmol. 1998; 236: 248–254
Messmer EP, Font RL, Kirkpatrick JB, Hopping W Immunohistochemical demonstration of neuronal and astrocytic differentiation in retinoblastoma. Ophthalmology. 1985; 92: 167–173
Messmer EP, Laqua H, Wessing A et al. Nine cases of cavernous hemangioma of the retina. Am J Ophthalmol 1983; 95: 383–390
Messmer EP, Font RL, Laqua H, Höppng W, Naumann GOH. Cavernous hemangioma of the retina. Immunohistochemical and ultrastructural observations. Arch Ophthalmol 1984; 102:413–418
Meyer-Schwickerath G, Lund OE, Wessing A, von Barsewisch B. Classification and terminology of ophthalmological changes in the retinal periphery. Mod Probl Ophthalmol 1975; 15:50–52
Michaelides M, Luthert PJ, Cooling R, Firth H, Moore AT. Norrie disease and peripheral venous insufficiency. Br J Ophthalmol. 2004; 88: 1475
Michels RG. Vitrectomy for macular pucker. Ophthalmology 1984; 91: 1364–1388
Michels RG. A clinical and histopathological study of epiretinal membranes affecting the macula and removed by vitreous surgery. Trans Am Ophthalmol Soc 1982; 80: 580–656
Michels S, Michels R, Simader C, Schmidt-Erfurth U. Verteporfin therapy for choroidal hemangioma: a long-term followup. Retina. 2005; 25: 697–703
Mieler WF, Will BR, Lewis H, Aaberg TM. Vitrectomy in the management of peripheral uveitis. Ophthalmology 1988; 95: 859–864
Miki D, Hida T, Hotta K, Shinoda K, Hirakata A. Comparison of scierai buckling and vitrectomy for retinal detachment resulting from flap tears in superior quadrants. Jpn J Ophthalmol 2001; 45:187–191
Miyamoto K, Khosrof S, Bursell SE, Rohan R, Murata T, Clermont AC, Aiello LP, Ogura Y, Adamis AP. Prevention of leukostasis and vascular leakage in streptozotocin-induced diabetic retinopathy via intercellular adhesion molecule-1 inhibition. Proc Natl Acad Sci USA. 1999; 96: 10836–10841
Miyamoto K, Refolo MF, Tolentino FI, Fournier GA, Albert DM. Perfluoroether liquid as a long-term vitreous substitute. An experimental study. Retina 1984; 4: 264–268
Montero JA, Ruiz-Moreno JM. Optical coherence tomography characterisation of idiopathic central serous chorioretinopathy. Br J Ophthalmol. 2005; 89:562–564
Mooy CM, De Jong PT. Prognostic parameters in uveal melanoma: a review. Surv Ophthalmol. 1996; 41: 215–228
Morino I, Hiscott P, McKechnie N, Grierson I. Variation in epiretinal membrane components with clinical duration of the proliferative tissue. Br J Ophthalmol. 1990; 74: 393–399
Murakami-Nagasako F, Ohba N. Phakic retinal detachment associated with cystic retinal tuft. Graefes Arch Clin Exp Ophthalmol. 1982; 219:188–192
Murphree AL, Villablanca JG, Deegan WF 3rd, Sato JK, Malogolowkin M, Fisher A, Parker R, Reed E, Gomer CJ. Chemotherapy plus local treatment in the management of intraocular retinoblastoma. Arch Ophthalmol. 1996; 114; 1348–1356
Nahib, M, Peyman GA, Clark LC, Hoffmann RE, Miceli M, Abou-Steit M. Experimental evaluation of perfluoro-phenanthrene as a high specific gravity vitreous substitute: a preliminary report. Ophthalmic Surg 1989; 20: 289–293
Nahum MP, Gdal-On M, Kuten A, Herzl G, Horovitz Y, Weyl Ben Arush M. Long-term follow-up of children with retinoblastoma. Pediatr Hematol Oncol. 2001; 18: 173–179
Nakamura K, Refojo MF, Crabtree DV. Factors contributing to the emulsification of intraocular silicone and fluorosilicone oils. Invest Ophthalmol Vis Sci. 1990; 31: 647–656
Nathwani BN, Kim H, Rappaport H, Solomon J, Fox M. Non-Hodgkin’s lymphomas: a clinicopathologic study comparing two classifications. Cancer. 1978; 41: 303–325
Naumann G, Hellner KA, Naumann LR. Pigmented Nevi of the Choroid. Clinical Study of Secondary Changes in the Overlying Tissue. Trans Am Acad Ophthalmol 1971; 75: 110–123
Naumann G, Yanoff M, Zimmerman LE. Histogenesis of Malignant Melanomas of the Uvea. I. Histopathologic Characteristics of Nevi of the Choroid and Ciliary Body. Arch Ophthalmol 1966; 76: 784–796
Naumann GO H, Seibel, W. Surgical Revision of Vitreous and Iris-Incarceration in Persisting Cystoid Maculopathy (Hruby-Irvine-Gass Syndrome) — report on 27 eyes. Dev Ophthalmol 1985; 11: 181–187
Naumann GOH and Völcker HE. Endophthalmitis haemogranulomatosa (eine spezielle Reaktion auf intraokulare Blutungen). Klin Mbl Augenheilkd 1977; 171: 352–359
Newman DK, Burton RL. Primary vitrectomy for pseudophakic and aphakic retinal detachments. Eye 1999; 13 (Pt 5):635–639
Newman E, Reichenbach A. The Muller cell: a functional element of the retina. Trends Neurosci. 1996; 19: 307–312
Nicholson DH, Galvis V (1984) Criswick-Schepens syndromes (familial exudative vitreoretinopathy): a study of a Colombian kindred. Arch Ophthalmol 102:1519–1522
Ninomiya Y, Lewis JM, Hasegawa T, Tanoi Y. Retinotomy and foveal translocation for surgical management of subfoveal choroidal neovascular membranes. Am J Ophthalmol. 1996; 122:613–621
Noda Y, Hata Y, Hisatomi T, Nakamura Y, Hirayama K, Miura M, Nakao S, Fujisawa K, Sakamoto T, Ishibashi T. Functional properties of hyalocytes under PDGF-rich conditions. Invest Ophthalmol Vis Sci. 2004; 45: 2107–2114
Nork TM, Millecchia LL, de Venecia GB, Myers FL, Vogel KA. Immunocytochemical features of retinoblastoma in an adult. Arch Ophthalmol. 1996; 114: 1402–1406
Nork TM, Millecchia LL, Strickland BD, Linberg JV, Chao GM. Selective loss of blue cones and rods in human retinal detachment. Arch Ophthalmol. 1995; 113: 1066–1073
Nork TM, Wallow IH, Sramek SJ, Stevens TS, De Venecia G. Immunocytochemical study of an eye with proliferative vitreoretinopathy and retinal tacks. Retina. 1990; 10: 78–85
Norton EWD, Fuller DG. The use of intraocular sulphur hexafluoride in vitrectomy. In Irvine AR, O’Malley C eds.: Advances in vitreous surgery, Springfield, III, 1976; Charles C Thomas Lecture
Novak MA, Rice TA, Michels RG, Auer C. The crystalline lens after vitrectomy for diabetic retinopathy. Ophthalmology. 1984; 91: 1480–1484
Noyes HD. Detachment of the macula with laceration of the macula lutea. Trans Am Ophthalmol Soc 1971; 1:128–134
Ohlmann A, Scholz M, Goldwich A, Chauhan BK, Hudl K, Ohlmann AV, Zrenner E, Berger W, Cvekl A, Seeliger MW, Tamm ER. Ectopic norrin induces growth of ocular capillaries and restores normal retinal angiogenesis in Norrie disease mutant mice. J Neurosci. 2005; 25:1701–1710
Ohira A, de Juan E Jr. Characterization of glial involvement in proliferative diabetic retinopathy. Ophthalmologica. 1990; 201: 187–195
Ohlmann AV, Adamek E, Ohlmann A, Lutjen-Drecoll E. Norrie gene product is necessary for regression of hyaloid vessels. Invest Ophthalmol Vis Sci. 2004; 45: 2384–2390
Oldendoerp J, Spitznas M: Factors influencing the results of vitreous surgery in diabetic retinopathy. I. Iris rubeosis and/ or active neovascularization at the fundus. Graefes Arch Clin Exp Ophthalmol 1989; 227: 1–8
O’Malley PF, Allen RA. Peripheral cystoid degeneration of the retina. Incidence and distribution in 1,000 autopsy eyes. Arch Ophthalmol. 1967; 77: 769–776
Oosterhuis JA, Journee-de Korver HG, Keunen JE. Transpupillary thermotherapy: results in 50 patients with choroidal melanoma. Arch Ophthalmol. 1998; 116: 157–162
Orrellana J, Lieberman RM. Stage III macular hole surgery. Br J Ophthalmol 1993; 77: 555–558
Oshima Y, Emi K, Motokura M, Yamanishi S. Survey of surgical indications and results of primary pars plana vitrectomy for rhegmatogenous retinal detachments. Jpn J Ophthalmol 1999; 43:120–126.
Oshima Y, Emi K, Motokura M, Yamanishi S. [A comparative study of visual outcomes following primary vitrectomy and scierai buckling procedures to manage macular off rhegmatogenous retinal detachments]. Nippon Ganka Gakkai Zasshi 1999; 103:215–222
Paques M, Chastang C, Mathis A, Sahel J, Massin P, Dosquet C, Korobelnik JF, Le Gargasson JF, Gaudric A. Effect of autologous platelet concentrate in surgery for idiopathic macular hole: results of a multicenter, double-masked, randomized trial. Platelets in Macular Hole Surgery Group. Ophthalmology. 1999; 106:932–938
Park DW, Dugel PU, Garda J, Sipperley JO, Thach A, Sneed SR, Blaisdell J. Macular pucker removal with and without internal limiting membrane peeling: pilot study. Ophthalmology. 2003; 110:62–64
Pearlstone AD. The incidence of idiopathic preretinal macular gliosis. Am Ophthalmol 1985; 17: 378–380
Pearson R, Jagger J. Sex linked juvenile retinoschisis with optic disc and peripheral retinal neovascularisation. Br J Ophthalmol. 1989; 73: 311–313
Pe’er J, Neufeld M, Baras M, Gnessin H, Itin A, Keshet E. Rubeosis iridis in retinoblastoma. Histologie findings and the possible role of vascular endothelial growth factor in its induction. Ophthalmology. 1997; 104: 1251–1258
Perentes E, Herbort CP, Rubinstein LJ, Herman MM, Uffer S, Donoso LA, Collins VP. Immunohistochemical characterization of human retinoblastomas in situ with multiple markers. Am J Ophthalmol. 1987; 103: 647–658
Perrier M, Sebag M. Epiretinal membrane surgery assisted by trypan blue. Am J Ophthalmol 2003; 135: 909–911
Pesin SR, Shields JA. Seven cases of trilateral retinoblastoma. Am J Ophthalmol. 1989; 107: 121–126
Peyman GA, Blinder KJ, Paris CJ, Alturki W, Nelson NC, Desai U. A technique for retinal pigment epithelium transplantation for age-related macular degeneration secondary to extensive subfoveal scarring. Ophthalmic Surg. 1991; 22: 102
Peyman GA, Cheema R, Conway MD, Fang T. Triamcinolone acetonide as an aid to visualization of the vitreous and the posterior hyaloid during pars plana vitrectomy. Retina 2000; 20:554–555
Piccolino FC, de la Longrais RR, Ravera G, Eandi CM, Ventre L, Abdollahi A, Manea M. The foveal photoreceptor layer and visual acuity loss in central serous chorioretinopathy. Am J Ophthalmol. 2005; 139: 87–99
Potter MJ, Myckatyn SO, Maberley AL, Lee AS. Vitrectomy for pars planitis complicated by vitreous hemorrhage: visual outcome and long-term follow-up. Am J Ophthalmol, 2001; 131:514–515
Poulaki V, Qin W, Joussen AM, Hurlbut P, Wiegand SJ, Rudge J, Yancopoulos GD, Adamis AP. Acute intensive insulin therapy exacerbates diabetic blood-retinal barrier breakdown via hypoxia-inducible factor-lalpha and VEGF. J Clin Invest. 2002; 109:805–815
Pournaras CJ, Donati G, Sekkat L, Kapetanios AD. Décollement de rétine du pseudophake. Traitement par vitrectomie et cerclage. Étude pilote. J. Fr. Ophtalmol. 2000; 23:1006–1011
Prescher G, Bornfeld N, Becher R. Nonrandom chromosomal abnormalities in primary uveal melanoma. J Natl Cancer Inst. 1990; 82: 1765–1769
Prescher G, Bornfeld N, Horsthemke B, Becher R. Chromosomal aberrations defining uveal melanoma of poor prognosis. Lancet. 1993; 339: 691–692
Prescher G, Bornfeld N, Becher R. Two subclones in a case of uveal melanoma. Relevance of monosomy 3 and multiplication of chromosome 8q. Cancer Genet Cytogenet. 1994 Oct 15;77(2):144–146
Prescher G, Bornfeld N, Hirche H, Horsthemke B, Jockei KH, Becher R. Prognostic implications of monosomy 3 in uveal melanoma. Lancet. 1996 May 4;347(9010):1222–1225
Qiao H, Hisatomi T, Sonoda KH, Kura S, Sassa Y, Kinoshita S, Nakamura T, Sakamoto T, Ishibashi T. The characterisation of hyalocytes: the origin, phenotype, and turnover. Br J Ophthalmol. 2005; 89: 513–517
Qualman SJ, Mendelsohn G, Mann RB, Green WR. Intraocular lymphomas. Natural history based on a clinicopathologic study of eight cases and review of the literature. Cancer. 1983; 52: 878–886
Quinn RH, Quong JN, Miller SS. Adrenergic receptor activated ion transport in human fetal retinal pigment epithelium. Invest Ophthalmol Vis Sci. 2001; 42: 255–264
Quivey JM, Augsburger J, Snelling L, Brady LW. 1251 plaque therapy for uveal melanoma. Analysis of the impact of time and dose factors on local control. Cancer. 1996; 77: 2356–2362
Rehm HL, Gutierrez-Espeleta GA, Garcia R, Jimenez G, Khetarpal U, Priest JM, Sims KB, Keats BJ, Morton CC. Norrie disease gene mutation in a large Costa Rican kindred with a novel phenotype including venous insufficiency. Hum Mutat 1997; 9: 402–408
Rehm HL, Zhang DS, Brown MC, Burgess B, Halpin C, Berger W, Morton CC, Corey DP, Chen ZY. Vascular defects and sensorineural deafness in a mouse model of Norrie disease. J Neurosci 2002; 22: 4286–4292
Reese AB, Jones IS, Cooper WC. Macular changes secondary to vitreous traction. Am J Ophthalmol. 1967; 64: 544–549
Remé CE, Braschler UF, Roberts JE, Dillon J. Light damage in the rat retina: Effect of radioprotective agent (WR77913) on acute rod outer segment disk disruptions. Photochem Photobiol 1991; 54: 137–142
Rhodes RH. A light microscopic study of the developing human neural retina. Am J Anat. 1979; 154: 195–209
Ricci A. Classification des degenerescences vitreo-retiniennes et chorio-retiniennes en relation avec le decollement de retine. Bibl Ophthalmol. 1969; 79:183–205
Rice TA, de Bustros S, Michels RG, et al. Prognostic factors in vitrectomy for epiretinal membranes of the macula. Ophthalmology 1986; 93: 602–610
Rice TA, Michels RG, Rice EF: Vitrectomy for diabetic traction retinal detachment involving the macula. Am J Ophthalmol 1983, 95:22–33
Richter M, Gottanka J, May CA, Welge-Lussen U, Berger W, Lutjen-Drecoll E. Retinal vasculature changes in Norrie disease mice. Invest Ophthalmol Vis Sci 1998; 39: 2450–2457
Rinkoff J, Machemer R, Hida T, Chandler D. Temperature-dependent light damage to the retina. Am J Ophthalmol. 1986; 102:452–462
Rivett K, Kruger L, Radioff S. Infracyanine green-assisted internal limiting membrane peeling in macular hole surgery: does it make a difference? Graefes Arch Clin Exp Ophthalmol 2004; 242: 393–396
Roider J, Hoerauf H, Hager A, Hoerboth T, Laqua H. Konventionelle Ablatiochirurgie oder primäre Vitrektomie bei komplizierten Lochsituationen Ophthalmologe 2001; 98: 887–891
Romayanada N, Goldberg MF, Green WR. Histopathology of sickle cell retinopathy. Trans Am Acad Ophthalmol Otolaryngol. 1973; 77: OP642–676
Rosen PH, Wong HC, McLeod D. Indentation microsurgery: internal searching for retinal breaks. Eye 1989; 3 (Pt 3): 277–281
Rosengren B, Osterlin S. Hydrodynamic events in the vitreous space accompanying eye movements. Significance for the pathogenesis of retinal detachment. Ophthalmologica 1976: 173:513–517.
Roth AM, Foos RY. Surface wrinkling retinopathy in eyes enucleated at autopsy. Trans Am Acad Ophthalmol Otolaryngol 1971; 75: 824–829
Roth M, Trittibach P, Koerner F, Sarra G. Pars-plana-Vitrektomie bei idiopathischen Glaskörpertrübungen. Klin Monatsbl Augenheilkd. 2005; 222: 728–732
Rowlatt U. Intrauterine wound healing in a 20 week human fetus. Virchows Arch A Pathol Anat Histo 1381:1979; 353–361
Ruby AJ, Williams DF, Grand MG, et al. Pars plana vitrectomy for treatment of stage 2 macular holes. Arch Ophthalmol 1994; 112:359–364
Rutzen AR, Ortega-Larrocea G, Dugel PU, Chong LP, Lopez PF, Smith RE, Rao NA. Clinicopathologic study of retinal and choroidal biopsies in intraocular inflammation. Am J Ophthalmol. 1995;119: 597–611
Ryan EH, Gilbert HD. Results of surgical treatment of recent onset full-thickness idiopathic macular holes. Arch Ophthalmol 1994; 112: 1545–1553
Ryan SJ. The development of an experimental model of subretinal neovascularization in disciform macular degeneration. Trans Am Ophthalmol Soc. 1979; 77: 707–745
Sach J, Krepelkova J, Kuchynka P. Haemangiosarcoma of the breast, metastatic to the ciliary body and iris. Br J Ophthalmol. 1998; 82:709–711
Sakamoto T, Miyazaki M, Hisatomi T, Nakamura T, Ueno A, Itaya K, Ishibashi T. Triamcinolone-assisted pars plana vitrectomy improves the surgical procedures and decreases the postoperative blood-ocular barrier breakdown. Graefes Arch Clin Exp Ophthalmol 2002; 240: 423–429
Sakamoto T, Sakamoto M, Yoshikawa H, Hata Y, Ishibashi T, Ohnishi Y, Inomata H. Histologic findings and prognosis of uveal malignant melanoma in Japanese patients. Am J Ophthalmol. 1996;121:276–283
Saornil MA, Egan KM, Gragoudas ES, Seddon JM, Walsh SM, Albert DM. Histopathology of proton beam-irradiated vs enucleated uveal melanomas. Arch Ophthalmol. 1992; 110: 1112–1118
Sarks JP, Sarks SH, Killingsworth MC. Evolution of geographic atrophy of the retinal pigment epithelium. Eye. 1988; 2: 552–577
Sarks JP, Sarks SH, Killingsworth MC. Evolution of soft drusen in age-related macular degeneration. Eye. 1994; 8:269–283
Sarks SH. Ageing and degeneration in the macular region: a clinico-pathological study. Br J Ophthalmol. 1976; 60: 324–341
Sarthy V. Collagen IV mRNA expression during development of the mouse retina: an in situ hybridization study. Invest Ophthalmol Vis Sci. 1993; 34: 145–152
Sato H, Kawasaki R, Yamashita H. Observation of idiopathic full-thickness macular hole closure in early postoperative period as evaluated by optical coherence tomography. Am J Ophthalmol. 2003; 136: 185–187
Sautter H, Lüllwitz W, Naumann G. Die Infrarot-Photographie in der Differential-Diagnose pigmentierter, tumorverdächtiger Fundusveränderungen. Klin Monatsbl Augenheilkd 1974; 164:597–602
Schachat AP, Oyakawa RT, Michels RG, Rice TA. Complications of vitreous surgery for diabetic retinopathy. II. Postoperative complications. Ophthalmology. 1983; 90: 522–530
Schatz H, McDonald HR. Atrophie macular degeneration. Rate of spread of geographic atrophy and visual loss. Ophthalmology. 1989; 96: 1541–1551
Scheider A, Gündisch O, Kampik A. Surgical extraction of subfoveal choroidal new vessels and submacular haemorrhage in age-related macular degeneration: results of a prospective study. Graefe’s Arch Clin Exp Ophthalmol. 1999; 237:10–15
Schepens CL. Diagnostic and prognostic factors as found in preoperative examination. Trans Am Acad Ophthalmol Otolaryngol 1952; 56: 398–418
Schiff WM, Chang S, Mandava N, Barile GR. Pars plana vitrectomy for persistent, visually significant vitreous opacities. Retina. 2000; 20: 591–596
Schilling H, Sauerwein W, Lommatzsch A, Friedrichs W, Brylak S, Bornfeld N, Wessing A. Long-term results after low dose ocular irradiation for choroidal haemangiomas. Br J Ophthalmol. 1997; 81: 267–273
Schilling H, Sehu KW, Lee WR. A histologie study (including DNA quantification and Ki-67 labeling index) in uveal melanomas after brachytherapy with ruthenium plaques. Invest Ophthalmol Vis Sci. 1997; 38: 2081–2092
Schlötzer-Schrehardt U, Viestenz Arne, Naumann GOH, Laqua H, Michels S, Schmidt-Erfurth U. Dose-related structural effects of photodynamic therapy on choroidal and retinal structures of human eyes. Graefes Arch Clin Exp Ophthalmol 2002; 240: 748–757
Schmidt-Erfurth U, Laqua H, Schlötzer-Schrehardt U, Viestenz A, Naumann GOH. Histopathological changes following photodynamic therapy in human eyes. Arch Ophthalmol 2002; 120:835–844
Schmidt-Erfurth U, Schlötzer-Schrehardt U, Cursiefen C, Michels S, Beckendorf A, Naumann GOH. Influence of photodynamic therapy on expression of vascular endothelial growth factor (VEGF), VEGF receptor 3, and pigment epithelium-derived factor. Invest Ophthalmol Vis Sci 2003; 44: 4473–4480
Schmidt JC, Rodrigues EB, Hoerle S, Meyer CH, Kroll P. Primary vitrectomy in complicated rhegmatogenous retinal detachment — a survey of 205 eyes. Ophthalmologica 2003; 217:387–392
Scholes AG, et al. Monosomy 3 in uveal melanoma: correlation with clinical and histologie predictors of survival. Invest Ophthalmol Vis Sci, 2003. 44(3): p. 1008–1011
Scholes AG, et al. Allelic imbalance at tumour suppressor loci in uveal melanoma. Ophthalmic Research, 1999. 31(Suppl. 1): p. 135
Scholes AG et al. Loss of heterozygosity on chromosomes 3, 9, 13 and 17, including the retinoblastoma locus, in uveal melanoma. Invest Ophthalmol Vis Sci, 2001. 42(11): p. 2472–2477
Schueler AO, Jurklies C, Heimann H, Wieland R, Havers W, Bornfeld N. Thermochemotherapy in hereditary retinoblastoma. Br J Ophthalmol. 2003;87: 90–95
Schultz GS, Grant MB. Neovascular growth factors. Eye. 1991; 5: 170–180
Scott IU, Flynn HW Jr, Murray TG, Smiddy WE, Davis JL, Feuer WJ. Outcomes of complex retinal detachment repair using 1000-vs 5000-centistoke silicone oil. Arch Ophthalmol. 2005; 123:473–478
Scott IU, Flynn HW, Jr., Azen SP, Lai MY, Schwartz S and Trese MT. Silicone oil in the repair of pediatric complex retinal detachments: a prospective, observational, multicenter study. Ophthalmology 1999; 106: 1399–1407
Scott JD. Lens epithelial proliferation in retinal detachment. Trans Ophthalmol Soc UK. 1982; 102 Pt 3: 385–389
Sebag J. Classifying posterior vitreous detachment: a new way to look at the invisible. Br J Ophthalmol 1997; 81: 527–532
Sebag J. Age-related differences in the human vitreoretinal interface. Arch Ophthalmol 1991; 15: 100–107
Sebag J. Age-related differences in the human vitreoretinal interface. Arch Ophthalmol. 1991; 109: 966–971
Sebag J, Balazcs EA: Morphology and ultrastructure of human vitreous fibers. Invest Ophthalmol Vis Sci 1989; 30:1867–1871
Sebag J. Balazs EA. Human vitreous fibres and vitreoretinal disease. Trans Ophthalmol Soc UK. 1985; 104: 123–128
Seregard S, Spangberg B, Juul C, Oskarsson M. Prognostic accuracy of the mean of the largest nucleoli, vascular patterns, and PC-10 in posterior uveal melanoma. Ophthalmology. 1998; 105:485–491
Shah M, Foreman DM and Ferguson MW Control of scarring in adult wounds by neutralising antibody to transforming growth factor beta. Lancet 1992; 339: 213–214
Sharma T, Gopa IL, Badrinath SS. Primary vitrectomy for rhegmatogenous retinal detachment associated with choroidal detachment. Ophthalmology 1998; 105:2282–2285
Shastry BS, Hiraoka M, Trese MT. Lack of association of the Norrie disease gene with retinoschisis phenotype. Jpn J Ophthalmol. 2000;44: 627–629
Sheidow TG, Hooper PL, Crukley C, Young J, Heathcote JG. Expression of vascular endothelial growth factor in uveal melanoma and its correlation with metastasis. Br J Ophthalmol. 2000; 84: 750–756
Shields CL, Sun H, Demirci H, Shields JA. Factors predictive of tumor growth, tumor décalcification, choroidal neovascularization, and visual outcome in 74 eyes with choroidal osteoma. Arch Ophthalmol. 2005; 123: 1658–1666
Shields CL, Shields JA, De Potter P, Quaranta M, Freire J, Brady LW, Barrett J. Plaque radiotherapy for the management of uveal metastasis. Arch Ophthalmol. 1997; 115: 203–209
Shields CL, Shields JA, Baez KA, Cater J, De Potter PV. Choroidal invasion of retinoblastoma: metastatic potential and clinical risk factors. Br J Ophthalmol. 1993; 77: 544–548
Shields CL, Shields JA, Minelli S, De Potter P, Hernandez C, Cater J, Brady L. Regression of retinoblastoma after plaque radiotherapy. Am J Ophthalmol. 1993; 115: 181–187
Shields CL, Shields JA, Karlsson U, Menduke H, Brady LW. Enucleation after plaque radiotherapy for posterior uveal melanoma. Histopathologic findings. Ophthalmology. 1990; 97: 1665–1670
Shields CL, Shields JA, Augsburger JJ. Choroidal osteoma. Surv Ophthalmol. 1988; 33: 17–27
Shields JA, Shields CL, Honavar SG, Demirci H. Clinical variations and complications of Coats disease in 150 cases: the 2000 Sanford Gifford Memorial Lecture. Am J Ophthalmol. 2001; 131:561–571
Shields JA, Stephens RF, Eagle RC Jr, Shields CL, De Potter P. Progressive enlargement of a circumscribed choroidal hemangioma. A clinicopathologic correlation. Arch Ophthalmol. 1992; 110: 1276–1278
Shields JA, Shields CL, Parsons H, Giblin ME. The role of photocoagulation in the management of retinoblastoma. Arch Ophthalmol. 1990; 108: 205–208
Shields JA, Shields CL. Treatment of retinoblastoma with cryotherapy. Trans Pa Acad Ophthalmol Otolaryngol. 1990; 42: 977–980
Sisley K, et al. Abnormalities of chromosomes 3 and 8 in posterior uveal melanoma correlate with prognosis. Genes Chromosom Cancer, 1997. 19: p. 22–28
Sisley K, Cottam DW, Rennie IG, Parsons MA, Potter AM, Potter CW, Rees RC. Non-random abnormalities of chromosomes 3,6, and 8 associated with posterior uveal melanoma. Genes Chromosomes Cancer. 1992; 5: 197–200
Sisley K, Rennie IG, Parsons MA, Jacques R, Hammond DW, Bell SM, Potter AM, Rees RC. Abnormalities of chromosomes 3 and 8 in posterior uveal melanoma correlate with prognosis. Genes Chromosomes Cancer. 1997; 19: 22–28
Smiddy WE, Feuer W Incidence of cataract extraction after diabetic vitrectomy. Retina. 2004; 24: 574–581
Smiddy WE, Michels RG, Gilbert HD, Green WR. Clinicopathologic study of idiopathic macular pucker in children and young adults. Retina. 1992; 12: 232–236
Smiddy WE, Flynn HW Jr, Nicholson DH, Clarkson JG, Gass JD, Olsen KR, Feuer W. Results and complications in treated retinal breaks. Am J Ophthalmol 1991; 112:623–631
Smiddy WE, Michels RG, Green WR. Morphology, pathology, and surgery of idiopathic vitreoretinal macular disorders. Retina 1990; 10:288–296
Smiddy WE, Michels RG, de Bustros S, et al. Histopathology of tissue removed during vitrectomy for impending idiopathic macular holes. Am J Ophthalmol 1989; 108: 360–364
Smiddy WE, Stark WJ, Michels RG, Maumenee AE, Terry AC, Glaser BM. Cataract extraction after vitrectomy. Ophthalmology 1987; 94: 483–487
Smiddy WE. Contusion in monkeys, Kap. 11
Soulieres D, Rousseau A, Tardif M, Larochelle M, Tremblay M, Vaillancourt L, Pelletier G. The radiosensitivity of uveal melanoma cells and the cell survival curve. Graefes Arch Clin Exp Ophthalmol. 1995; 233: 85–89
Speicher MA, Fu AD, Martin JP, von Fricken MA. Primary vitrectomy alone for repair of retinal detachments following cataract surgery. Retina 2000; 20:459–464
Spira AW, Hollenberg MJ. Human retinal development: ultrastructure of the inner retinal layers. DevBiol. 1973; 31:1–21
Spitznas M, Meyer-Schwickerath G, Stephan B: The clinical picture of Eales’ disease. Graefes Arch Clin Exp Ophthalmol 1975; 194(2): 73–85.
Spraul CW, Lang GE, Grossniklaus HE, Lang GK. Histologic and morphometric analysis of the choroid, Bruch’s membrane, and retinal pigment epithelium in postmortem eyes with age-related macular degeneration and histologic examination of surgically excised choroidal neovascular membranes. Surv Ophthalmol. 1999; 44: S10–32
Stalmans P, Van Aken EH, Melles G, Veckeneer M, Feron EJ, Stalmans I. Trypan blue not toxic for retinal pigment epithelium in vitreo. Am J Ophthalmol 2003; 135: 234–236
Staudt S, Miller DW, Unnebrink K, Holz FG. Inzidenz und Ausprägung von postoperativem Makulaödem nach Makulaforamenoperation mit und ohne kombinierte Kataraktoperation. Ophthalmologe. 2003; 100: 702–707
Stefansson E, Hatchell DL, Fisher BL, Sutherland FS, Machemer R. Panretinal photocoagulation and retinal oxygenation in normal and diabetic cats. Am J Ophthalmol. 1986; 101:657–664
Stefansson E, Novack RL, Hatchell DL. Vitrectomy prevents retinal hypoxia in branch retinal vein occlusion. Invest Ophthalmol Vis Sci. 1990; 31: 284–289
Stefansson E. Oxygen and diabetic eye disease. Graefes Arch Clin Exp Ophthalmol. 1990; 228: 120–123
Stefansson E. The therapeutic effects of retinal laser treatment and vitrectomy. A theory based on oxygen and vascular physiology. Acta Ophthalmol Scand. 2001; 79: 435–440
Stelnicki EJ, Arbeit J, Cass DL, Saner C, Harrison M and Largman C. Modulation of the human homeobox genes PRX-2 and HOXB13 in scarless fetal wounds. J Invest Dermatol 1998; 111:57–63
Stone J, Chan-Ling T, Pe’e r J, Itin A, Gnessin H, Keshet E. Roles of vascular endothelial growth factor and astrocyte degeneration in the genesis of retinopathy of prematurity. Invest Ophthalmol Vis Sci. 1996; 37: 290–299
Stone J, Dreher Z. Relationship between astrocytes, ganglion cells and vasculature of the retina. J Comp Neurol 1987; 255: 35–49
Straatsma BR, Foos RY, Feman SS (1986) Degenerative disease of the peripheral retina. In Duane DD (ed): Clinical ophthalmol. Vol.3, Chapter 26, Philadelphia, 1986, Harper & Row, 1–16
Straatsma BR, Foos RY and Feman SS. Degenerative disease of the peripheral retina. In: Duane DD (ed): Clinical Ophthalmol. Vol. 3, Chapter 26, Philadelphia, 1986, Harper & Row, 1–19
Straatsma BR, Foos RY. Typical and reticular retinoschisis. Am J Ophthalmol 1973; 75: 551–575
Straatsma BR, Zeegen, Foos RY, Feman SS, Shabo AL. Lattice degeneration of the retina. XXX Edward Jackson Memorial Lecture. Am J Ophthalmol 1974; 77: 619–649
Strahlman ER, Fine SL, Hillis A. The second eye of patients with senile macular degeneration. Arch Ophthalmol. 1983; 101: 1191–1193
Strauss O. The retinal pigment epithelium in visual function. Physiol Rev. 2005; 85: 845–881
Streilein JW, Ma N, Wenkel H, Ng TF, Zamiri P. Immunobiology and privilege of neuronal retina and pigment epithelium transplants. Vision Res. 2002; 42:487–495
Surgery Trial Research Group. Surgery for subfoveal choroidal neovascularization in age-related macular degeneration. Ophthalmic findings: SST Report No.11 Ophthalmology. 2004; 111: 1967–1980
Szurman P, Di Tizio FM, Lafaut B, Aisenbrey S, Grisanti S, Roters S, Bartz-Schmidt KU. Notwendigkeit der Kopftieflage nach Makulaforamenchirurgie: eine konsekutive Fall-Kontroll Studie. Klin Monatsbl Augenheilkd. 2000; 217:351–355
Takada Y, Fariss RN, Tanikawa A, Zeng Y, Carper D, Bush R, Sieving PA. A retinal neuronal developmental wave of retinoschisin expression begins in ganglion cells during layer formation. Invest Ophthalmol Vis Sci. 2004; 45: 3302–3312
Takeuchi A, Kricorian G, Marmor MF. Albumin movement out of the subretinal space after experimental retinal detachment. Invest Ophthalmol Vis Sci. 1995; 36:1298–1305
Tanner V, Minihan M, Williamson TH. Management of inferior retinal breaks during pars plana vitrectomy for retinal detachment. Br J Ophthalmol 2001; 85: 480–482
The Collaborative Ocular Melanoma Study (COMS) randomized trial of pre-enucleation radiation of large choroidal melanoma III: local complications and observations following enucleation COMS report no. 11. Am J Ophthalmol. 1998; 126:362–372
The Collaborative Ocular Melanoma Study (COMS) randomized trial of pre-enucleation radiation of large choroidal melanoma II: initial mortality findings. COMS report no. 10. Am J Ophthalmol. 1998;125: 779–796
The Collaborative Ocular Melanoma Study (COMS) randomized trial of pre-enucleation radiation of large choroidal melanoma I: characteristics of patients enrolled and not enrolled. COMS report no. 9. Am J Ophthalmol. 1998; 125: 767–778
Theodossiadis PG, Georgalas IG, Emfietzoglou J, Kyriaki TE, Pantelia E, Gogas PS, Moschos MN, Theodossiadis GP. Optical coherence tomography findings in the macula after treatment of rhegmatogenous retinal detachments with spared macula preoperatively. Retina. 2003; 23:69–75
Thomas JW, Grossniklaus HE, Lambert HM, Aaberg TM, L’Hernault N. Ultrastructural features of surgically excised idiopathic subfoveal. Retina. 1993; 13: 93–98
Thomas MA, Dickinson JD, Melberg NS, Ibanez HE, Dhaliwal RS. Visual results after surgical removal of subfoveal choroidal membranes. Ophthalmology. 1994; 101: 1384–1396
Thomas MA, Grand MG, Williams DF, Lee CM, Pesin SR, Lowe MA. Surgical management of subfoveal choroidal neovascularization. Ophthalmology. 1992; 99: 952–968
Thompson JT. Epiretinal membrane removal in eyes with good visual acuities. Retina. 2005; 25: 875–882
Thompson JT. The role of patient age and intraocular gas use in cataract progression after vitrectomy for macular holes and epiretinal membranes. Am J Ophthalmol. 2004; 137: 250–257
Thumann G, Aisenbrey S, Schraermeyer U, et al. Transplantation of autologous iris pigment epithelium after removal of choroidal neovascular membranes. Arch Ophthalmol. 2000; 118: 1350–1355
Tielsch JN, Legro LW, Cassard SD. Risk factors for retinal detachment after cataract surgery. A population based case controlled study. Ophthalmology 1996; 103: 1537–1545
Tillery WV and Lucier LC. Round atrophic holes in lattice degeneration — an important cause of phakic retinal detachment. Trans Am Acad Ophthalmol Otolaryngol 1976; 81: 509–518
Tolentino F, Schepens CL and Freeman HN. Vitreoretinal disorders diagnosis and management, W.B. Saunders, Philadelphia 1976; p 340–349
Tolentino FI, Lapus JV, Novalis G, Trempe CL, Gutow GS, Ahmad A. Fluorescein angiography of degenerative lesions of the peripheral fundus and rhegmatogenous retinal detachment. Int Ophthalmol Clin. 1976; 16: 13–29
Trick GL, Berkowitz BA. Retinal oxygenation response and retinopathy. Prog Retin Eye Res. 2005; 24: 259–274
Tschentscher F, Husing J, Holter T, Kruse E, Dresen IG, Jockei KH, Anastassiou G, Schilling H, Bornfeld N, Horsthemke B, Lohmann DR, Zeschnigk M. Tumor classification based on gene expression profiling shows that uveal melanomas with and without monosomy 3 represent two distinct entities. Cancer Res 2003; 63:2578–2584
Tso MO. Clues to the cells of origin in retinoblastoma. Int Ophthalmol Clin. 1980; 20: 191–210
van Bockxmeer FM, Martin CE, Thompson DE and Constable IJ. Taxol for the treatment of proliferative vitreoretinopathy. Invest Ophthalmol Vis Sci 26: 1985; 1140–1147
van Effenterre G, Haut J, Larricart P, Abi-Rached J, Vachet JM. Gas tamponade as a single technique in the treatment of retinal detachment: is vitrectomy needed? A comparative study of 120 cases. Graefes Arch Clin Exp Ophthalmol 1987; 225: 254–258
Van Meurs JC, ter Averst E, Croxen R, Hofland L, van Hagen PM. Comparison of the growth potential of retinal pigment epithelial cells obtained during vitrectomy in patients with age-related macular degeneration or complex retinal detachment. Graefes Arch Clin Exp Ophthalmol 2004; 242: 442–443
van Meurs JC, Bolt BJ, Mertens DA, Peperkamp E, De Waard P. Rubeosis of the iris in proliferative vitreoretinopathy. Retina. 1996; 16:292–295
van Meurs JC, Schwoerer J, Schwartz B, Mulder PG, Meiselmann HJ, Johnson CS. Retinal vessel autoregulation in sickle cell patients. Graefes Arch Clin Exp Ophthalmol. 1992; 230:442–445.
van Meurs JC. Relationship between peripheral vascular closure and proliferative retinopathy in sickle cell disease. Graefes Arch Clin Exp Ophthalmol. 1991; 229: 543–538
van Nouhuys CE (1991) Signs, complications, and platelet aggregation in familial exudative vitreoretinopathy. Am J Ophthalmol 111:34–41
van Nouhuys CE (1989) Juvenile retinal detachment as a complication of familial exudative vitreoretinopathy. Fortschr Ophthalmol 86:221–223
van Nouhuys CE (1982) Dominant exudative vitreoretinopathy and other vascular developmental disorders of the peripheral retina. Doc Ophthalmol 54:1–414
van Nouhuys CE (1981) Congenital retinal fold as a sign of dominant exudative vitreoretinopathy. Graefes Arch Clin Exp Ophthalmol 217:55–67
van Velthoven ME, Verbraak FD, Garcia PM, Schlingemann RO, Rosen RB, de Smet MD. Evaluation of central serous retinopathy with en face optical coherence tomography. Br J Ophthalmol. 2005 Nov; 89(11):1483–1488.
Veckeneer M, van Overdam K, Monzer J, Kobuch K, van Marie W, Spekreijse H, van Meurs J. Ocular toxicity of trypan blue injected into the vitreous cavity of rabbit eyes. Graefes Arch Clin Exp Ophthalmol 2001; 239: 698–704
Velikay M, Stolba U, Wedrich A, Li Y, Datlinger P, Binder S. The effect of chemical stability and purification of perfluorocarbon liquids in experimental extended-term vitreous substitution. Graefes Arch Clin Exp Ophthalmol. 1995; 233:26–30
Velikay M, Wedrich A, Stolba U, Datlinger P, Li Y, Binder S. Experimental long-term vitreous replacement with purified and non purified Perfluorodecaline. Am J Ophthalmol 1993; 116:565–570
Vogel M. Treatment of malignant choroidal melanomas with photocoagulation. Evaluation of ten-year follow-up data. Am J Ophthalmol 1972; 74:1
Vogel M. Histopathologic observation of photocoagulated malignant melanomas of the choroid. Am J Ophthalmol 1972; 74: 468
Vogt A. Die Operative Therapie und Die Pathogenese der Netzhautablösung. Stuttgart Ferdinand Enke Verlag, 1936
von Domarus D, Mitschke H. Primäres alveolares Weichteilsarkom der Aderhaut. Ophthalmologie und Histiogenese. Ophthalmologica 1978; 177: 229–235
Warburg M, Hauge M, Sänger R. Nome’s disease and the XG blood group system: linkage data. Acta Genet Stat Med. 1965; 15:103–115
Warwar RE, Bullock JD, Shields JA, Eagle RC Jr. Coexistence of 3 tumors of neural crest origin: neurofibroma, meningioma, and uveal malignant melanoma. Arch Ophthalmol. 1998; 116: 1241–1243
Weinstock SJ, Morin JD. Traumatic macular hole. Can J Ophthalmol. 1976; 11:249–251
Weller M, Wiedemann P and Heimann K. Proliferative vitreoretinopathy — is it anything more than wound healing at the wrong place? Int Ophthalmol 1990; 14: 105–117
Wells JA, Gregor ZJ. Surgical treatment of full-thickness macular holes using autologous serum. Eye 1996; 10: 593–599.
Wendel RT, Patel AC, Kelly NE, Salzano TC, Wells JW, Novack GD. Vitreous surgery for macular holes. Ophthalmology 1993; 100: 1671–1676
Wenkel H, Streilein JW. Evidence that retinal pigment epithelium functions as an immune-privileged tissue. Invest Ophthalmol Vis Sci. 2000; 41:3467–3473
Wenkel H, Streilein JW, Young MJ. Systemic immune deviation in the brain that does not depend on the integrity of the blood-brain barrier. J Immunol. 2000; 164:5125–5131
Wenkel H, Chen PW, Ksander BR, Streilein JW. Immune privilege is extended, then withdrawn, from allogeneic tumor cell grafts placed in the subretinal space. Invest Ophthalmol Vis Sci. 1999; 40:3202–3208
Wenkel H, Naumann GO. Retrolaminäre Infiltration des Sehnervenkopfes nach Silikonöltamponade. Klin Monatsbl Augenheilkd. 1999; 214: 120–122
Wenkel H, Streilein JW. Analysis of immune deviation elicited by antigens injected into the subretinal space. Invest Ophthalmol Vis Sci. 1998; 39:1823–1834
West H, Richardson WD, Fruttiger M. Stabilization of the retinal vascular network by reciprocal feedback between blood vessels and astrocytes. Development. 2005; 132:1855–1862
Whitcup SM, de Smet MD, Rubin BI, Palestine AG, Martin DF, Burnier M Jr, Chan CC, Nussenblatt RB. Intraocular lymphoma. Clinical and histopathologic diagnosis. Ophthalmology. 1993; 100: 1399–1406
Whitcup SM, Park WS, Gasch AT, Eagle RC, Filie AC, Nussenblatt RB, Zhuang Z, Chan CC. Use of microdissection and molecular genetics in the pathologic diagnosis of retinoblastoma. Retina. 1999; 19: 318–324
White VA, et al. Correlation of cytogenetic abnormalities with the outcome of patients with uveal melanoma. Cancer, 1998. 83: p. 354–359
Wiedemann P, Hilgers RD, Bauer P, Heimann K. Adjunctive daunorubicin in the treatment of proliferative vitreoretinopathy: results of a multicenter clinical trial. Am J Ophthalmol 1998; 126:550–559
Wiedemann P and Heimann K. Proliferative Vitreoretinopathie. Pathogenese und Möglichkeiten der Zytostatikatherapie. Klin Monatsbl Augenheilkd 1986; 188: 559–564
Wieger G. Über den Canalis petiti und ein Ligamentum hyaloideocapsulare (dissertation) Strassburg 1883
Wilkes SR, Beard CN, Kurland LT. The incidence of retinal detachment in Rochester, Minnesota, 1970–1978. Am J Ophthalmol 1982; 94: 670–673
Wilkinson CP. Evidence-based analysis of prophylactic treatment of asymptomatic retinal breaks and lattice degeneration. Ophthalmology 2000; 107:12–15
Williams RG, Chang S, Comaratta MR and Simoni G. Does the presence of heparin and dexamethasone in the vitrectomy infusate reduce reproliferation in proliferative vitreoretinopathy? Graefes Arch Clin Exp Ophthalmol 1996; 234: 496–503
Williamson TH. Vitreous surgery in uveitis and allied disorders. In: Kirchhof B, Wong D (eds): Vitreo-retinal surgery, Essentials in Ophthalmology Series, Springer, Berlin 2005, pp 163–174
Winter M, Eberhardt W, Scholz C, Reichenbach A. Failure of potassium siphoning by Muller cells: a new hypothesis of perfluorocarbon liquid-induced retinopathy. Invest Ophthalmol Vis Sci. 2000; 41: 256–261
Witschel H, Font RL. Hemangioma of the choroid. A clinicopathologic study of 71 cases and review of the literature. Surv Ophthalmol 1976; 20: 415–431
Wolf S, Lappas A, Weinberger AW, Kirchhof B. Macular translocation for surgical management of subfoveal choroidal neovascularizations in patients with AMD: first results. Graefes Arch Clin Exp Ophthalmol. 1999; 237: 51–57
Wolfensberger TJ. Foveal reattachment after macula-off retinal detachment occurs faster after vitrectomy than after buckle surgery. Ophthalmology. 2004; 111:1340–1343
Wong D, Stanga P, Briggs M, Lenfestey P, Lancaster E, Li KK, Lim KS and Groenewald C. Case selection in macular relocation surgery for age related macular degeneration. Br J Ophthalmol 2004; 88: 186–190
Wong HC, Sehmi KS, McLeod D. Abortive neovascular outgrowths discovered during vitrectomy for diabetic vitreous haemorrhage. Graefes Arch Clin Exp Ophthalmol. 1989; 227: 237–240
Worley LA, Onken MD, Person E, Robirds D, Branson J, Char DH, Perry A, Harbour JW. Transcriptomic versus cromosomal prognostic markers and clinical outcome in uveal melanoma. Clin Cancer Res 2007; 13:1466–1471
Worst JGF: The bursa intravitrealis premacularis. New Developments in Ophthalmology. Nijmegen, Doc Ophthalmol Proc Ser 1975; 275–279
Worst JGF, Sebag J, Kishi S, Shimizi K: posterior vitreous pocket: Correspondence. Arch Ophthalmol 1991; 109:1058–1060
Yamada E. Some structural features of the fovea centralis in the human retina. Arch Ophthalmol 1969; 82: 152–159
Yang CM, Pars plana vitrectomy in the treatment of combined rhegmatogenous retinal detachment and choroidal detachment in aphakic or pseudophakic patients. Ophthalmic Surg Lasers 1997; 28: 288–293
Yanoff M. Pseudogliomas: differential diagnosis of retinoblastoma: Ophthal. Dig. 1972; 34: 9
Yanhoff M and Zimmerman LE, Davis RL. Massive gliosis of the retina. Int Ophthalmol Clin 1971; 11: 211
Yanoff M, EK Rahn, LE Zimmerman: Histopathology of juvenile retinoschisis. Arch. Ophthalmol 79 (1968):49–53
Yaoeda H. Clinical observation on macular hole. Acta Soc Ophthalmol Jpn 1967; 71: 1723–1736
Yilmaz S, Horsthemke B, Lohmann DR. Twelve novel RB1 gene mutations in patients with hereditary retinoblastoma. Mutations in brief no. 206. Hum Mutat. 1998; 12: 434
Young TL, Anthony DC, Pierce E, Foley E, Smith LE. Histopathology and vascular endothelial growth factor in untreated and diode laser-treated retinopathy of prematurity. J AAPOS. 1997; 1:105–110
Zeana D, Becker J, Kuckelkorn R, Kirchhof B. Perfluorohexyloctane as a long-term vitreous tamponade in the experimental animal. International Ophthalmology 1999; 23: 17–24
Zimmerman LE, McLean IW, Foster WD. The Manschot-van Peperzeel concept of the growth and metastasis of uveal melanomas. Doc Ophthalmol. 1980; 50: 101–121
Zimmerman LE, McLean IW, Foster WD. Does enucleation of the eye containing a malignant melanoma prevent or accelerate the dissemination of tumour cells. Br J Ophthalmol. 1978; 62: 420–425
Zimmerman LE, Naumann GOH. Pathology of Retinoschisis in “New and Controversial Aspects of Retinal Detachment”, McPherson A (ed), New York, Hoeber, 400–423, 1968
Zimmerman LE, Spencer WH. The pathologic anatomy of retinoschisis. Arch Ophthalmol 1960; 63: 10–19
Zografos L, Bercher L, Chamot L, Gailloud C, Raimondi S, Egger E. Cobalt-60 treatment of choroidal hemangiomas. Am J Ophthalmol. 1996; 121: 190–199
References
Annesley W, Brown G, Boiling J, Goldberg R, Fisher D. Treatment of retinal detachment with congenital optic pit by krypton laser photocoagulation. Graefes Arch Clin Exp Ophthalmol 1987. 225;5: 311–314
Brodsky MC. Morning glory disc anomaly or optic disc coloboma? Arch Ophthalmol 1994. 112;2: 153
Burk RO, Rendon R. Clinical detection of optic nerve damage. Surv Ophthalmol 2004. 45;3: 297–303
Cohen AI. Is there a potential defect in the blood retinal barrier at the choroidal level of the optic nerve canal? Invest Ophthal 1973; 12: 513
Corbett JJ, Thompson HS. The rational management of idiopathic intracranial hypertension. Arch Neurol 1989. 46;10: 1049–1051
Dichtl A, Jonas JB, Holbach L, Naumann GOH. Retinal nerve fiber layer thickness in human eyes. Graefes Arch Clin Exp Ophthalmol 1999. 237;6: 474–479
Eller AW, Friberg TL, Mah F. Migration of silicone oil into the brain. Am J Ophthalmol 2002; 133: 429–438
Evans JM, Batts KP, Hunder GG. Persistent giant cell arteritis despite corticosteroid treatment. Mayo Clin Proc 1994. 69;11: 1060–1061
Friedmann SM, Margo CE. Bilateral subinternal limiting membrane hemorrhage with Terson syndrome. Am J Ophthalmol 1997. 124;6: 850–851
Gandorfer A, Kampik A. Role of vitreoretinal interface in the pathogenesis and therapy of macular disease associated with optic pits. Ophthalmologe 2000. 97;4: 276–279
Glaser JS, Teimory M, Schatz NJ. Optic nerve sheath fenestration for progressive optic neuropathy. Results in second series consisting of 21 eyes. Arch Ophthalmol 1994. 112;8: 1047–1050
Green WR, Chan CC, Hutchins GM, Terry JM. Central vein occlusion: A prospective histopathologic study of 29 eyes in 28 cases. Retina 1981. 1;1: 27–55
Heiduschka P, Fischer D, Thanos S. Recovery of visual evoked potentials after regeneration of cut ganglion cell axons within the ascending visual pathway in rats. Restorative Neurology and Neuroscience 2005. 23;5–6: 303–312
Hinzpeter EN, Naumann GOH. Ischemic papilledema in giant cell arteriitis. Mucopolysaccharide deposition with normal intraocular pressure. Arch Ophthalmol 1976; 94: 624–628
Horio N, Horiguchi M. Retinal blood flow and macular edema after radial optic neurotomy for central retinal vein occlusion. Am J Ophthalmol 2006. 141;1: 31–34
Hotta K. Unsuccessful vitrectomy without gas tamponade for macular retinal detachment and retinoschisis without optic disc pit. Ophthalmic Surg Lasers Imaging. 2004 Jul–Aug;35(4):328–331
Irvine AR, Crawford JB, Sullivan JH. The pathogenesis of retinal detachment with morning glory discs and pit. Retina 1986. 6;3: 146–150
Ishikawa K, Terasaki H, Mori M, Sugita K, Miyake Y. OCT before and after vitrectomy with internal limiting membrane removal in a child with optic pit maculopathy. Jpn J Ophthalmol 2005. 49;5: 411–413
Jacobs DS, Foster CS. Temporal arteriitis. In: Alber DM, Jacobiec FA (eds) Principles and practice of ophthalmology, vol.5. Philadelphia: Saunders 1994; 2901–2908
Jonas JB, Berenshtein E, Holbach L. Lamina cribrosa thickness and spatial relationships between intraocular space and cerebrospinal fluid space in highly myopic eyes. Invest Ophthalmol Vis Sci 2004. 45;8: 2660–2665
Jonas JB, Naumann GOH. The optic nerve: Its embryology, histology and morphology. In: Varma R, Spaeth GL (eds) The optic nerve in glaucoma. Philadelphia: Lippincott 1993; pp 3–26
Jonas JB, Schmidt AM, Müller-Bergh JA, Schlötzer-Schrehardt UM, Naumann GOH. Human optic nerve fiber count and optic disc size. Invest Ophthalmol Vis Sci 1992. 33;6: 2012–2018
Kearns TP, Hollenhorst RW. Venous stasis retinopathy of occlusive disease of the carotid artery. Majo Clinic Proc 1963;38:304
Kim TW, Lee SJ, Kim SD. Comparative evaluation of radial optic neurotomy and panretinal photo coagulation in the management of central vein occlusion. Korean J Ophthalmol 2005. 19;4: 269–274
Konno S, Akiba J, Sato E, Kuriyama S, Yoshida A. OCT in successful surgery of retinal detachment associated with optic nerve head pit. Ophthalmic Surg Lasers 2000. 31;3:236–239
Kubota T, Holbach L, Naumann GOH. Corpora amylacea in glaucomatous and non-glaucomatous optic nerve and retina. Graefes Arch Clin Exp Ophthalmol 1993. 231;1: 7–11
Kubota T, Jonas JB, Naumann GOH. Direct clinico-histological correlation of parapapillary chorioretinal atrophy. Br J Ophthalmol 1993. 77;2: 103–106
Kuhn F, Morris R, Witherspoon CD, Mester V. Terson syndrome. Results of vitrectomy and the significance of vitreous hemorrhage in patients with subarachnoid hemorrhage. Ophthalmology 1998. 105;3: 472–477
Lippe von der I, Wuermeling MJ, Naumann GOH. Akute druckabhängige Veränderungen des neuroretinalen Randsaums in einer juvenilen Glaukompapille — Messungen mittels Laser Scanning Tomographie und planimetrischer Papillometrie. Klin Monatsbl Augenheilkd 1994; 204:126–130
Naumann GOH, Mardin CY, Bergua A. Bedeutung und Perspektive der Glaukom-Mikrozirkulationsforschung. Klin Monatsbl Augenheilkd 1993; 203: 286
Naumann GOH. Benign melanocytoma of the optic nerve papilla. Doc Ophthalmol. 1966;20: 468–483
Okinami S, Ohkuma M, Tsukahara I. Kuhnt intermediary tissue as a barrier between the optic nerve and retina. Albrecht v Graefes Arch klin exp Ophthal 1977; 201: 57
Opremcak EM, Rehmar AJ, Ridenour CD, Kurz DE. Radial optic neurotomy for central retinal vein occlusion: 117 consecutive cases. Retina 2006. 26;3: 297–305
Postel EA, Pulido JS, McNamara JA, Johnson MW. The etiology and treatment of macular detachment associated with optic nerve pits and related anomalies. Trans Am Ophthalmol Soc 1998; 96:73–88
Quigley HA. The pathogenesis of reversible cupping in congenital glaucoma. Am J Ophthalmol 1977;84:358
Richardson KT, Shaffer RN. Optic nerve cupping in congenital glaucoma. Am J Ophthalmol 1966;62:507
Risco JM, Grimson BS, Johnson PT. Angioarchitecture of the ciliary artery circulation of the posterior pole. Arch Ophthalmol 1981. 99;5: 864–868
Seiff SR, Shah L. A model for the mechanism of optic nerve fenestration. Arch Ophthalmol 1990. 108;9: 1326–1329
Sharma T, Gopal L, Biswas J, Shanmugam MP, Bhende PS, Agrawal R, Shetty NS, Sanduja N. Results of vitrectomy in Terson’s syndrome. Ophthalmic Surg Lasers 2002. 33;3: 195–199
Traboulsi El, O’Neill JF. The spectrum in the morphology of the so called morning glory disc anomaly. J Pediatr Ophthalmol Strabismus 1988. 25;2: 93–98
Tsai JC, Petrovich MS, Sadun AA. Histopathological and ultrastructural examination of optic nerve sheath decompression. Br J Ophthalmol 1995. 79;2: 182–185
Vogel A, Holz G, Loeffler KU. Histopathologic findings after radial optic neurotomy in central retinal vein occlusion. Am J Ophthalmol 2006. 141;1: 203–205
Wenkel H, Michelson G. Korrelation der Ultraschallbiomikroskopie mit histologischen Befunden in der Diagnostik der Riesenzellarteriitis. Klin Monatsbl Augenheilkd 1996; 210:48–52
Wenkel H, Naumann GOH. Retrolaminäre Infiltration des Nervus opticus durch als intraokulare Tamponade verwendetes Silikonöl. Klin Monatsbl Augenheilkd 1999; 214: 120–122
Wietholter S, Steube D, Stotz HP. Terson syndrome: A frequently missed ophthalmologic complication in subarachnoid hemorrhage. Zentrabl Neurochir 1998. 59;3: 166–170
Wrede J, Varadi G, Volcker HE, Dithmar S. Radial optic neurotomy for central retinal vein occlusion — how deep should it be. Ophthalmologe 2006. 103;4: 321–324
Yokoi M, Kase M, Hyodo T, Horimoto M, Kitagawa F, Nagata R. Epiretinal membrane formation in Terson’s syndrome. Jpn J Ophthalmol 1997. 41;3: 168–173
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2008 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Cursiefen, C. et al. (2008). Special Anatomy and Pathology in Intraocular Microsurgery. In: Naumann, G.O.H., Holbach, L.M., Kruse, F.E. (eds) Applied Pathology for Ophthalmic Microsurgeons. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-68366-7_5
Download citation
DOI: https://doi.org/10.1007/978-3-540-68366-7_5
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-540-24189-8
Online ISBN: 978-3-540-68366-7
eBook Packages: MedicineMedicine (R0)