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- W4379137853 abstract "THE demonstration of the association of inherited deficiencies of erythrocyte enzymes with certain congenital hemolytic anemias has aided a greater understanding of the genetic and pathological manifestations of these disorders, and has resulted in a more definitive classification of these heterogeneous conditions. In 1954 Selwyn and Dacie1 separated the congenital nonspherocytic hemolytic anemias into two classes, Types 1 and 2, on the basis of differences in the spontaneous autohemolysis of sterile defibrinated blood. Valentine, Tanaka and Miwa,2 , 3 in 1961, described the occurrence of a marked deficiency of erythrocyte pyruvate kinase in association with hemolytic disease classifiable as Type 2 on . . ." @default.
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- W4379137853 date "1965-02-04" @default.
- W4379137853 modified "2023-10-17" @default.
- W4379137853 title "Hereditary Hemolytic Anemia with Triosephosphate Isomerase Deficiency" @default.
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- W4379137853 doi "https://doi.org/10.1056/nejm196502042720503" @default.
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