Remarques sur les enzymopathies génétiques du globule rouge
- 1 January 1972
- Vol. 54 (5-6) , 765-773
- https://doi.org/10.1016/s0300-9084(72)80182-2
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Purification and properties of pyruvate kinase in normal and in pyruvate kinase deficient human red blood cellsBiochimica et Biophysica Acta (BBA) - Enzymology, 1971
- Electrophoretic and functional variants of NADH-methemoglobin reductase in hereditary methemoglobinemiaJournal of Clinical Investigation, 1971
- Klinische und biochemische Untersuchungen zur Glucosephosphatisomerasc normaler menschlicher Erythrocyten und bei Glucosephosphatisomerase-MangelKlinische Wochenschrift, 1970
- Clinical Profile: Hereditary Hemolytic Disorders and Enzymatic Deficiencies of Human ErythrocytesBlood, 1970
- Heterogeneity of the Enzymatic Defect in Congenital MethemoglobinemiaNew England Journal of Medicine, 1969
- Les anomalies de la glycolyse au cours de l'anémie hémolytique par déficit du globule rouge en pyruvate kinaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1968
- Tissue Distribution of Human Pyruvate Kinase IsozymesEnzymologia Biologica Et Clinica, 1968
- Electrophoresis of red cell NADH- and NADPH-diaphorases in normal subjects and patients with congenital methemoglobinemiaBiochemical and Biophysical Research Communications, 1967
- Mental Retardation in Methemoglobinemia Due to Diaphorase DeficiencyNew England Journal of Medicine, 1965
- Space-Time Relationships in Somesthetic LocalizationScience, 1956