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5. Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes. Miwa S; Fujii H Am J Hematol; 1996 Feb; 51(2):122-32. PubMed ID: 8579052 [TBL] [Abstract][Full Text] [Related]
6. Red cell enzymopathies as a model of inborn errors of metabolism. Miwa S; Kanno H; Hirono A; Fujii H Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():112-9. PubMed ID: 8629088 [TBL] [Abstract][Full Text] [Related]
8. G6PD/PK ratio: a reliable parameter to identify glucose-6-phosphate dehydrogenase deficiency associated with microcytic anemia in heterozygous subjects. Tagarelli A; Piro A; Tagarelli G; Bastone L; Paleari R; Mosca A Clin Biochem; 2004 Oct; 37(10):863-6. PubMed ID: 15369716 [TBL] [Abstract][Full Text] [Related]
9. Infectious disease: a cause of hemolytic anemia in glucose-6 phosphate dehydrogenase deficiency. Burka ER Ann Intern Med; 1969 Jan; 70(1):222-5. PubMed ID: 5763723 [No Abstract] [Full Text] [Related]
10. Detection of G6PD and pyruvate kinase deficiencies in reticulocytosis by reference to erythrocyte creatine. Brewster MA; Berry DH Clin Biochem; 1981 Jun; 14(3):132-4. PubMed ID: 7296823 [TBL] [Abstract][Full Text] [Related]
11. Red cell glucose-6-phosphate dehydrogenase status and pyruvate kinase activity in a Nigerian population. May J; Meyer CG; Grossterlinden L; Ademowo OG; Mockenhaupt FP; Olumese PE; Falusi AG; Luzzatto L; Bienzle U Trop Med Int Health; 2000 Feb; 5(2):119-23. PubMed ID: 10747271 [TBL] [Abstract][Full Text] [Related]
13. Clinical utility of fractionating erythrocytes into "Percoll" density gradients. Mosca A; Paleari R; Modenese A; Rossini S; Parma R; Rocco C; Russo V; Caramenti G; Paderi ML; Galanello R Adv Exp Med Biol; 1991; 307():227-38. PubMed ID: 1666816 [TBL] [Abstract][Full Text] [Related]
14. Glucose-6-phosphate dehydrogenase and red cell pyruvate kinase deficiency in neonatal jaundice cases in egypt. Abdel Fattah M; Abdel Ghany E; Adel A; Mosallam D; Kamal S Pediatr Hematol Oncol; 2010 May; 27(4):262-71. PubMed ID: 20426517 [TBL] [Abstract][Full Text] [Related]
15. Clinical and biochemical studies on mutant red cell enzymes mainly associated with hemolytic anemia. Miwa S Jinrui Idengaku Zasshi; 1980 Jun; 25(2):83-92. PubMed ID: 7431680 [No Abstract] [Full Text] [Related]
16. 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]
17. Haemolytic anaemia due to glucose-6-phosphate dehydrogenase (G6PD) deficiency: demonstration of two new biochemical variants, G6PD Hamm and G6PD Tarsus. Gahr M; Bornhalm D; Schröter W Br J Haematol; 1976 Jul; 33(3):363-70. PubMed ID: 1276080 [TBL] [Abstract][Full Text] [Related]
18. Pyruvate kinase deficiency. Association with G6PD deficiency. BMJ; 1992 Sep; 305(6856):760-2. PubMed ID: 1422333 [No Abstract] [Full Text] [Related]
19. [II. Chronic hemolytic anemia caused by erythrocytic deficiency of glucose-6-phosphate dehydrogenase (G6PD)]. Cutillo S Pediatria (Napoli); 1979 Dec; 87(4):V-VI. PubMed ID: 554049 [No Abstract] [Full Text] [Related]