Angeborene Enzymdefekte als Ursache von Bluterkrankungen

[1]  E. Beutler.  Effect of flavin compounds on glutathione reductase activity: in vivo and in vitro studies. , 1969, The Journal of clinical investigation.

[2]  O. Garson,et al.  Hereditary hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes and leukocytes. A probable X-chromosome-linked syndrome. , 1969, The New England journal of medicine.

[3]  S. Tarui,et al.  Enzymatic basis for the coexistence of myopathy and hemolytic disease in inherited muscle phosphofructokinase deficiency. , 1969, Biochemical and biophysical research communications.

[4]  R. G. Chapman.  Red Cell Aldolase Deficiency in Hereditary Spherocytosis , 1969, British journal of haematology.

[5]  J. Dacie.  HEREDITARY DISORDERS OF ERYTHROCYTE METABOLISM , 1969 .

[6]  A. Kraus,et al.  Red cell phosphoglycerate kinase deficiency. A new cause of non-spherocytic hemolytic anemia. , 1968, Biochemical and biophysical research communications.

[7]  R. Bracci,et al.  Hydrogen peroxide toxicity and detoxification in the erythrocytes of newborn infants. , 1967, Blood.

[8]  F. Oski,et al.  Hereditary hemolytic anemia with hexokinase deficiency. Role of hexokinase in erythrocyte aging. , 1967, The New England journal of medicine.

[9]  W. Valentine,et al.  Hereditary hemolytic anemia with triosephosphate isomerase deficiency: Studies in kindreds with coexistent sickle cell trait and erythrocyte glucose-6-phosphate dehydrogenase deficiency , 1966 .

[10]  P. Hochstein,et al.  GENERATION OF HYDROGEN PEROXIDE IN ERYTHROCYTES BY HEMOLYTIC AGENTS. , 1964, Biochemistry.

[11]  A. Robinson.  THE ASSAY OF GALACTOKINASE AND GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE ACTIVITY IN HUMAN ERYTHROCYTES , 1963, The Journal of Experimental Medicine.

[12]  Loehr Gw,et al.  A new enzymopenic hemolytic anemia with glutathione reductase deficiency , 1962 .

[13]  J. Loos,et al.  Hereditary Absence of Reduced Glutathione in the Erythrocytes — a New Clinical and Biochemical Entity? , 1961, Vox sanguinis.

[14]  C. Huguley,et al.  PYRIMIDINE METABOLISM IN MAN. IV. THE ENZYMATIC DEFECT OF OROTIC ACIDURIA. , 1961, The Journal of clinical investigation.

[15]  G. C. Mills.  Hemoglobin catabolism. I. Glutathione peroxidase, an erythrocyte enzyme which protects hemoglobin from oxidative breakdown. , 1957, The Journal of biological chemistry.

[16]  P. Carson,et al.  Enzymatic deficiency in primaquine-sensitive erythrocytes. , 1956, Science.

[17]  L. Flohé,et al.  Untersuchungen über die Glutathion:H 2 O 2 -Oxydoreduktase (Glutathion-Peroxydase) , 1967 .

[18]  H. Waller,et al.  Über die Diagnose von Glykogenosen aus der Glukose-6-Phosphatase-Aktivität und dem Glykogengehalt der Thrombozyten , 1962 .

[19]  Q. Gibson.  The reduction of methaemoglobin in red blood cells and studies on the cause of idiopathic methaemoglobinaemia. , 1948, The Biochemical journal.