EXTREME HEMOLYSIS AND RED-CELL DISTORTION IN ERYTHROCYTE PYRUVATE KINASE DEFICIENCY. I. MORPHOLOGY, ERYTHROKINETICS AND FAMILY ENZYME STUDIES.
D000743:Anemia, Hemolytic; D000746:Anemia, Hemolytic, Congenital Nonspherocytic; D001774:Blood Chemical Analysis; D002648:Child; D002859:Chromium Isotopes; D004796:Clinical Enzyme Tests; D004912:Erythrocytes; D005826:Genetics, Medical; D005955:Glucosephosphate Dehydrogenase Deficiency; D005958:Glucosephosphates; D006452:Hemoglobinometry; D006461:Hemolysis; D006801:Humans; D007501:Iron / Q000378:metabolism*; D008659:Metabolic Diseases; D010770:Phosphotransferases; D011770:Pyruvate Kinase / Q000172:deficiency; D015323:Pyruvate Metabolism, Inborn Errors
D002859:Chromium Isotopes; D005958:Glucosephosphates; D007501:Iron; D010770:Phosphotransferases; D011770:Pyruvate Kinase
ANEMIA, HEMOLYTIC; ANEMIA, HEMOLYTIC, CONGENITAL NONSPHEROCYTIC; BLOOD CHEMICAL ANALYSIS; CHILD; CHROMIUM ISOTOPES; ENZYME TESTS; ERYTHROCYTES; GENETICS, HUMAN; GLUCOSEPHOSPHATE DEHY- DROGENASE DEFICIENCY; HEMOGLOBINOMETRY; IRON METABOLISM; METABOLIC DISEASES; PHOSPHOTRANSFERASES; PYRUVATE KINASE