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Journal Abstract Search

408 related items for PubMed ID: 2307454

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  • 23. A new glucose-6-phosphate dehydrogenase variant, Gd(-) Tepic, characterized by moderate enzyme deficiency and mild episodes of hemolytic anemia.
    Lisker R, Pérez-Briceño R, Beutler E.
    Hum Genet; 1985; 69(1):19-21. PubMed ID: 3967887
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  • 24. A case of G6PD Utrecht associated with β-thalassemia responding to splenectomy.
    Yang K, Liu X, Chen K, Luo S, Kong W, Huang W, Xiao J.
    Pediatr Blood Cancer; 2022 Sep; 69(9):e29837. PubMed ID: 35695473
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  • 27. Two new variants of glucose-6-phosphate dehydrogenase associated with hereditary non-spherocytic hemolytic anemia: G6PD Wayne and G6PD Huron.
    Ravindranath Y, Beutler E.
    Am J Hematol; 1987 Apr; 24(4):357-63. PubMed ID: 3565372
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  • 28. Chronic severe hemolytic anemia due to G-6-PD Charleston: a new deficient variant.
    Beutler E, Grooms AM, Morgan SK, Trinidad F.
    J Pediatr; 1972 Jun; 80(6):1005-9. PubMed ID: 4402065
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  • 30. 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 Jun; 61(2):175-6. PubMed ID: 7129446
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  • 31. Gd(-) Carapicuiba, a rare glucose-6-phosphate dehydrogenase variant associated with moderate enzyme deficiency and chronic hemolysis.
    Barretto OC, Nonoyama K.
    Braz J Med Biol Res; 1991 Jun; 24(2):133-9. PubMed ID: 1823224
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  • 32. [A family of new glucose 6-phosphate dehydrogenase (G 6 PD) variant associated with chronic nonspherocytic hemolytic anemia: G 6 PD Kurume (author's transl)].
    Kaneto A, Motokawa M, Koga T, Shimokawa Y, Tanikawa K, Fujii H, Miwa S.
    Rinsho Ketsueki; 1979 Jan; 20(1):82-9. PubMed ID: 423378
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  • 38. Congenital nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency in a Japanese child. Clinical and metabolic studies.
    Kojima H.
    Nihon Ketsueki Gakkai Zasshi; 1972 Feb; 35(1):20-31. PubMed ID: 4264123
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  • 39. Molecular analysis of eight biochemically unique glucose-6-phosphate dehydrogenase variants found in Japan.
    Hirono A, Fujii H, Takano T, Chiba Y, Azuno Y, Miwa S.
    Blood; 1997 Jun 15; 89(12):4624-7. PubMed ID: 9192788
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  • 40. Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency.
    Filosa S, Giacometti N, Wangwei C, De Mattia D, Pagnini D, Alfinito F, Schettini F, Luzzatto L, Martini G.
    Am J Hum Genet; 1996 Oct 15; 59(4):887-95. PubMed ID: 8808605
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