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Journal Abstract Search
119 related items for PubMed ID: 2919631
1. Characterization of a new G6PD variant: G6PD Titusville. Csepreghy M, Hall MK, Berkow RL, Jackson S, Prchal JT. Am J Med Sci; 1989 Feb; 297(2):114-7. PubMed ID: 2919631 [Abstract] [Full Text] [Related]
11. Two apparent glucose-6-phosphate dehydrogenase variants in normal XY males: G6PD Alabama. Prchal JT, Hall K, Csepreghy M, Lilly M, Berkow R, Scott CW. Am J Med; 1988 Mar; 84(3 Pt 1):517-23. PubMed ID: 3348252 [Abstract] [Full Text] [Related]
13. Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP). Molecular study of a new variant (G6PD Clinic) with markedly acidic pH optimum. Vives-Corrons JL, Pujades MA, Petit J, Colomer D, Corbella M, Aguilar i Bascompte JL, Merino A. Hum Genet; 1989 Jan; 81(2):161-4. PubMed ID: 2912886 [Abstract] [Full Text] [Related]
14. Deficiency of glucose-6-phosphate dehydrogenase found in a case of hepatic fructose-1,6-diphosphatase deficiency. Kinugasa A, Kusunoki T, Iwashima A. Pediatr Res; 1979 Dec; 13(12):1361-4. PubMed ID: 230449 [Abstract] [Full Text] [Related]
15. G-6-PD Long Prairie: a new glucose-6-phosphate dehydrogenase mutant exhibiting normal sensitivity to inhibition by NADPH and accompanied by nonspherocytic hemolytic anemia. Johnson GJ, Kaplan ME, Beutler E. Blood; 1977 Feb; 49(2):247-51. PubMed ID: 12846 [Abstract] [Full Text] [Related]
17. A genetic variant of human erythrocyte glucose 6-phosphate dehydrogenase. Haghighi B, Suzangar M, Yazdani A, Mehnat M. Biochem Biophys Res Commun; 1985 Nov 15; 132(3):1151-9. PubMed ID: 4074350 [Abstract] [Full Text] [Related]
19. Glucose-6-phosphate dehydrogenase Lodi844C: a study on its expression in blood cells and muscle. Ninfali P, Bresolin N, Baronciani L, Fortunato F, Comi G, Magnani M, Scarlato G. Enzyme; 1991 Nov 15; 45(4):180-7. PubMed ID: 1823863 [Abstract] [Full Text] [Related]