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23. A new glucose-6-phosphate dehydrogenase variant (G6PD Iwate) associated with congenital non-spherocytic hemolytic anemia. Kanno H; Takano T; Fujii H; Tani K; Morisaki T; Hirono A; Kumakawa T; Ogura H; Takahashi K; Tsutsumi H Nihon Ketsueki Gakkai Zasshi; 1988 Jul; 51(4):715-9. PubMed ID: 3201886 [No Abstract] [Full Text] [Related]
24. Hereditary nonspherocytic hemolytic anemia due to a new hexokinase variant with reduced stability. Magnani M; Stocchi V; Cucchiarini L; Novelli G; Lodi S; Isa L; Fornaini G Blood; 1985 Sep; 66(3):690-7. PubMed ID: 4027385 [TBL] [Abstract][Full Text] [Related]
26. G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia. Vaca G; Ibarra B; Romero F; Olivares N; Cantú JM; Beutler E Hum Genet; 1982; 61(2):175-6. PubMed ID: 7129446 [TBL] [Abstract][Full Text] [Related]
27. A new variant of hereditary hemolytic anemia with stomatocytosis and erythrocyte cation abnormality. Miller DR; Rickles FR; Lichtman MA; La Celle PL; Bates J; Weed RI Blood; 1971 Aug; 38(2):184-204. PubMed ID: 5559828 [No Abstract] [Full Text] [Related]
31. Congenital nonspherocytic hemolytic anemia associated with an unusual erythrocyte hexokinase abnormality. Necheles TF; Rai US; Cameron D J Lab Clin Med; 1970 Oct; 76(4):593-602. PubMed ID: 5458022 [No Abstract] [Full Text] [Related]
32. [Congenital nonspherocytic hemolytic anemias caused by glucose-6-phosphate dehydrogenase deficiency of the erythrocytes in a Japanese family]. Abe T; Takafuji H; Yamamoto M; Daimon S; Nakajima K Blut; 1968 Jun; 17(3):143-51. PubMed ID: 5655443 [No Abstract] [Full Text] [Related]
33. [Heterogeneity of hereditary erythrocyte disorders and perspectives of its study]. Tokarev IuN Probl Gematol Pereliv Krovi; 1974 Oct; 19(10):3-6. PubMed ID: 4431762 [No Abstract] [Full Text] [Related]
34. The role of puberty in red-cell production in hereditary haemolytic anaemias. Shahidi NT; Clatanoff DV Br J Haematol; 1969 Oct; 17(4):335-42. PubMed ID: 5346406 [No Abstract] [Full Text] [Related]
35. A new glucose-6-phosphate dehydrogenase variant with congenital nonspherocytic hemolytic anemia (G6PD Genova). Biochemical characterization and mosaicism expression in the heterozygote. Gaetani GF; Galiano S; Melani C; Miglino M; Forni GL; Napoli G; Perrone L; Ferraris AM Hum Genet; 1990 Mar; 84(4):337-40. PubMed ID: 2307454 [TBL] [Abstract][Full Text] [Related]
36. Hereditary stomatocytosis: association of low 2,3-diphosphoglycerate with increased cation pumping by the red cell. Wiley JS; Cooper RA; Adachi K; Asakura T Br J Haematol; 1979 Jan; 41(1):133-41. PubMed ID: 420735 [TBL] [Abstract][Full Text] [Related]
37. Erythrocyte pyruvate kinase deficiency: relations of residual enzyme activity, altered regulation of defective enzymes and concentrations of high-energy phosphates with the severity of clinical manifestation. Lakomek M; Neubauer B; von der Lühe A; Hoch G; Winkler H; Schröter W Eur J Haematol; 1992 Aug; 49(2):82-92. PubMed ID: 1397245 [TBL] [Abstract][Full Text] [Related]
38. A case of congenital nonspherocytic hemolytic anemia associated with glucosephosphate isomerase (GPI) deficiency-GPI 'Kinki'. Takegawa S; Fujii H; Miwa S; Ohba Y; Yamauchi H; Miyata H Nihon Ketsueki Gakkai Zasshi; 1983 Feb; 46(1):11-7. PubMed ID: 6858560 [No Abstract] [Full Text] [Related]
39. Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: a new variant (type Nordhorn). I. Clinical and genetic studies. Schröter W; Koch HH; Wonneberger B; Kalinowsky W; Arnold A; Blume KG; Hüther W Pediatr Res; 1974 Jan; 8(1):18-25. PubMed ID: 4809302 [No Abstract] [Full Text] [Related]
40. Red cell glucose-6-phosphate dehydrogenase deficiency in Finland. Vuopio P; Härkönen M; Johnsson R; Nuutinen M Ann Clin Res; 1973 Jun; 5(3):168-73. PubMed ID: 4749241 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]