Pyruvate kinase deficiency and related disorders of red cell glycolysis
- 1 November 1966
- journal article
- research article
- Published by Elsevier in The American Journal of Medicine
- Vol. 41 (5) , 762-785
- https://doi.org/10.1016/0002-9343(66)90036-2
Abstract
No abstract availableThis publication has 57 references indexed in Scilit:
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- Increased Cell Membrane Permeability in the Pathogenesis of Hereditary Spherocytosis *Journal of Clinical Investigation, 1964
- A Case of Congenital Atypical Haemolytic Anaemia with Pyruvate Kinase DeficiencyVox Sanguinis, 1964
- Hereditary Non-Spherocytic Haemolytic Anaemia.British Journal of Haematology, 1964
- Extreme Hemolysis and Red-Cell Distortion in Erythrocyte Pyruvate Kinase DeficiencyNew England Journal of Medicine, 1964
- Studies in Congenital Non-Spherocytic Haemolytic Anaemias with Specific Enzyme DefectsActa Haematologica, 1964
- Erythrocyte Pyruvate Kinase Deficiency Resulting in Congenital Nonspherocytic Hemolytic AnemiaNew England Journal of Medicine, 1963
- Hereditary Non-spherocytic Hemolytic Anemia of the Pyruvate-kinase Deficient TypeAnnals of Internal Medicine, 1963
- RED‐CELL METABOLISM IN CONGENITAL HÆMOLYTIC ANÆMIASAustralasian Annals of Medicine, 1963
- Congenital Non Spherocytic Haemolytic Anaemia Due to Pyruvate-Kinase DeficiencyActa Haematologica, 1963