Molecular hybridization techniques in current diagnosis of chronic hepatitis B in childhood S. WirthB. Zabel Review Pages: 243 - 249
Transient cardiac constriction following purulent pericarditis A. AllariaD. MichelliD. Gutierrez Cardiology Pages: 250 - 251
Lethal junctional epidermolysis bullosa with normal expression of BM 600 and antro-pyloric atresia: A new variant of junctional epidermolysis bullosa? J. P. LacourP. HoffmanJ. P. Ortonne Dermatology Pages: 252 - 257
Development of height and weight in children with diabetes mellitus: Report on two prospective multicentre studies, one cross-sectional, one longitudinal A. ThonE. HeinzeJ. Nothjunge Endocrinology Pages: 258 - 262
Diagnostic value of growth hormone-releasing hormone test in children and adolescents with idiopathic growth hormone deficiency T. ArrigoF. MartinoF. De Luca Endocrinology Pages: 263 - 265
The association of hypopituitarism with small pituitary, invisible pituitary stalk, type 1 Arnold-Chiari malformation, and syringomyelia in seven patients born in breech position: a further proof of birth injury theory on the pathogenesis of “idiopathic hypopituitarism” K. FujitaN. MatsuoI. Hibi Endocrinology Pages: 266 - 270
Iatrogenic IgG2 deficiency in a leukaemic child A. W. de BoerG. A. M. de VaanJ. A. J. M. Bakkeren Hematology/Oncology Pages: 271 - 273
IgG subclass deficiency in children with recurrent bronchitis F. De BaetsJ. KintJ. Leroy Immunology/Allergology Pages: 274 - 278
Cytochrome b positive X-linked chronic granulomatous disease: A normal cell surface expression of cytochrome b H. AzumaH. OomiA. Okuno Immunology/Allergology Pages: 279 - 282
Spontaneous growth in turner syndrome: Evidence for a minor pubertal growth spurt G. HaeuslerM. SchemperE. Plöchl Medical Genetics Pages: 283 - 287
A family with one child with acrocallosal syndrome, one child with anencephaly-polydactyly, and parental consanguinity S. CataltepeE. Tuncbilek Medical Genetics Pages: 288 - 290
Defective monocyte oxidative metabolism in a child with Smith-Lemli-Opitz syndrome G. Zahle ØstergaardH. NielsenB. Friis Medical Genetics Pages: 291 - 294
The relationship of fluid restriction during the 1st month of life to the occurrence and severity of bronchopulmonary dysplasia in low birth weight infants: A 1-year radiological follow up O. K. T. TammelaF. P. LanningM. E. Koivisto Neonatology Pages: 295 - 299
Neonatal intestinal perforation due to congenital defects in the intestinal muscularis S. IzraeliE. FreudP. Merlob Neonatology Pages: 300 - 303
Intra-uterine long bone growth in small-for-gestational-age infants J. PalaciosS. RodríguezJ. I. Rodríguez Neonatology Pages: 304 - 307
Plasma exchange for fulminant Wilson disease J. SarlesP. LefevreG. Picon Letters to the Editors Pages: 310 - 310
Beta-mannosidosis and ethanolaminuria in a female patient H. WijburgJ. de JongR. Sengers Letters to the Editors Pages: 311 - 311
Dignity of the perinatal optimality score of Prechtl H. Manzke Letters to the Editors Pages: 311 - 311
Branchio-oculo-facial syndrome report of a new case with agenesis of cerebellar vermis D. MazzoneA. MilanaC. Carpinato Letters to the Editors Pages: 312 - 312
Haemorrhagic cystitis and urinary retention in Henoch-Schönlein purpura S. J. AllenA. SpriggD. C. Davidson Letters to the Editors Pages: 312 - 312
3-methylglutaconic aciduria in a patient with a disturbed mitochondrial energy metabolism J. A. J. M. BakkerenR. C. A. SengersR. H. Largo Letters to the Editors Pages: 313 - 313
Urinary N-acetyl-β-d-glucosaminidase activity in a girl with distal renal tubular acidosis E. RingW. ErwaM. Haim-Kuttnig Letters to the Editors Pages: 314 - 314
