Literatur
Carson, P. E., C. L. Flanagan, C. E. Ickes andA. S. Alving: Enzymatic deficiency in primaquine-sensitive erythrocytes. Science124, 484 (1956).
Cori, G. T., andC. F. Cori: Glucose-6-phosphatase of the liver in glycogen storage disease. J. biol. Chem.199, 661 (1952).
Dancis, J., J. Hutzler andM. Levitz: Metabolism of the white blood cells in maple syrup urine disease. Biochim. biophys. Acta (Amst.)43, 342 (1960).
Erbliche Stoffwechselkrankheiten. Genetic defects of biologically active proteins. Hrsg. vonF. Linneweh. München u. Berlin: Urban & Schwarzenberg 1962.
Fallon, H. J., M. Lotz andL. H. Smith: Congenital orotic aciduria: Demonstration of an enzyme defect in leukocytes and comparison with drug-induced orotic aciduria. Blood20, 700 (1962).
Gibson, Q. H.: The reduction of methemoglobin in red blood cells and studies on the cause of idiopathic methemoglobinemia. Biochim. J.42, 13 (1948).
Gross, R., W. Gerok, G. W. Löhr, W. Vogell, H. D. Waller u.W. Theopold: Über die Natur der Thrombasthenie. Klin. Wschr.38, 193 (1960).
Hülsmann, W. C., T. L. Olei andS. van Creveld: Phosphorylase activity in leukocytes from patients with glycogen storage disease. Lancet1961 II, 581.
Kalckar, H. M., B. Braganca andA. Munch-Petersen: Uridyl transferases and the formation of uridine diphosphogalactose. Nature (Lond.)172, 1038 (1953).
Kirsten, E., andR. Kirsten: A nanomole adaption of the automatic amino acid analysis according toSpackman, Stein andMoore. Biochem. biophys. Res. Commun.7, 76 (1962).
Kretchmer, N., M. Stone andCharles Bauer: hereditary enzymatic effects as illustrated by Hypophosphatasia. Ann. N.Y. Acad. Sci.75, 279 (1958/59).
Leloir, L. F.: InW. D. McElroy andB. Glass (Edit.), Phosphorus metabolism. Baltimore: Johns Hopkins Press 1951.
Linneweh, F.: Fortschritte in der Erkennung heterozygoter Merkmalsträger bei erblichen Enzymopathien. Klin. Wschr.40, 553 (1962).
Linneweh, F., G. W. Löhr, H. D. Waller u.R. Gross: Über die Diagnose der Glykogenose aus der Glucose-6-Phosphatase-Aktivität und dem Glykogengehalt der Thrombocyten. Encymol. biol. et clin.2, 188 (1962/63).
Linneweh, F., G. W. Löhr, H. D. Waller u.R. Gross: Heterozygoten-Test für Glykogenose (v. Gierkesche Krankheit). Klin. Wschr.41, 352 (1963).
Löhr, G. W.: Stoffwechseleigenschaften und Enzyme der Leukocyten des Menschen. Folia haemat. N.F.6, 49 (1961).
Löhr, G. W.: InF. Linneweh, Erbliche Stoffwechselkrankheiten. Genetic defects of biologically active proteins, S. 307. München u. Berlin: Urban & Schwarzenberg 1962.
Löhr, G. W., u.H. D. Waller: Eine neue enzymopenische hämolytische Anämie mit Glutathion-Reduktase-Mangel. Med. Klin.57, 1521 (1962).
Löhr, G. W., u.H. D. Waller: Glucose-6-phosphat-Dehydrogenase (Zwischenferment). In:H. U. Bergmeyer, Methoden der enzymatischen Analyse. Weinheim: Verlag Chemie 1962.
Prankerd, T. A. J.: Studies on the pathogenesis of haemolysis in hereditary spherocytosis. Quart. J. Med.29, 160 (1960).
Ramot, B., S. Fischer, A. Szeinberg, A. Adam, C. Sheba andD. Gafni: A study of subjects with erythrocyte glucose-6-phosphate dehydrogenase deficiency. II. Investigation of leukocyte enzymes. J. clin. Invest.38, 2234 (1959).
Ramot, B., A. Szeinberg, A. Adam, C. Sheba andD. Gafni: A study of subjects with erythrocyte glucose-6-phosphosphate dehydrogenase deficiency. Investigation of platelet enzymes. J. clin. Invest.38, 1659 (1959).
Rimington, C., andH. L. Booy: Porphyrin biosynthesis in human red cells. Biochem. J.65, 3 P (1957).
Schwarz, V., L. Goldberg, G. M. Komrower andA. Holzel: Metabolic observations on the erythrocytes from cases of galactosaemia. Biochem. J.59, XXII (1955).
Scott, E. M., andJ. V. Griffith; The enzymatic defect of hereditary methemoglobinemia: diaphorese. Biochim. biophys. Acta (Amst.)34, 584 (1959).
Sidbury, J. B., M. Cornblath, J. Fisher andE. House: Glycogen in erythrocytes of patients with glycogen storage disease. Pediatrics27, 103 (1961).
Smith, L. H. M. Sullivan andC. M. Huguley: Pyrimidine metabolism in man. IV. The enzymatic defect of orotic aciduria. J. clin. Invest.40, 656 (1961).
Soupart, P.: InJ. T. Holden, Amino acid pools, S. 220. Amsterdam-London-New York: Elsevier P.C. 1962.
Takahara, S.: InF. Linneweh, Erbliche Stoffwechselkrankheiten. Genetic defects of biologically active proteins, S. 535. München u. Berlin: Urban & Schwarzenberg 1962.
Tanaka, K. R., W. N. Valentine andSh. Miwa: Pyruvate kinase (PK) deficiency hereditary nonspherocytic hemolytic anemia. Blood19, 267 (1962).
Waller, H. D., G. W. Löhr, F. Grignani u.R. Gross: Über den Energiestoffwechsel normaler menschlicher Thrombocyten. Thrombos. Diathes. haemorrh. (Stuttg.)3, 520 (1959).
Waller, H. D., G. W. Löhr u.M. Tabatabai: Hämolyse und Fehlen von Glukose-6-Phosphatdehydrogenase in roten Blutzellen. (Eine Fermentanomalie der Erythrocyten.) Klin. Wschr.35, 1022 (1957).
Weinberg, A. N.: Detection of congenital galactosemia and the carrier state using galactose C14 and blood cells. Metabolism10, 728 (1961).
Westall, R. G., andS. Tomlinson: Vth Internat. Congr. Biochem. Abstr.16, 366 (1961).
Williams, H. E., andJ. B. Field: Low leukocyte phosphorylase in hepatic phosphorylase-deficient glycogen storage disease. J. clin. Invest.40, 1841 (1961).
Williams, H. E., E. M. Kendig andJ. B. Field: Leukocyte debranching enzyme in glycogen storage disease. J. clin. Invest.42, 656 (1963).
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Linneweh, F. Über die Rolle der Blutzellen in der Diagnostik erblicher Stoffwechselkrankheiten. Klin Wochenschr 41, 937–941 (1963). https://doi.org/10.1007/BF01478534
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DOI: https://doi.org/10.1007/BF01478534