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Journal Abstract Search

117 related items for PubMed ID: 241122

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  • 2. A new variant of glucose-6-phosphate dehydrogenase deficiency hereditary hemolytic anemia, G6PD Cornell: erythrocyte, leukocyte, and platelet studies.
    Miller DR, Wollman MR.
    Blood; 1974 Sep; 44(3):323-31. PubMed ID: 4152748
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  • 5. NADP+ and NADPH in glucose-6-phosphate dehydrogenase-deficient erythrocytes under oxidative stimulation.
    Mareni C, Gaetani GF.
    Biochim Biophys Acta; 1976 Jun 08; 430(3):395-8. PubMed ID: 7294
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  • 6. [Free nucleotides of erythrocytes in anemias in children. Results of 64 examinations].
    Orsini A, Vovan L, Itie R, Perrimond H.
    Arch Fr Pediatr; 1969 Jun 08; 26(9):993-1002. PubMed ID: 4391903
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  • 7. Reduction of oxidized glutathione in normal and glucose-6-phosphate dehydrogenase deficient erythrocytes and their hemolysates.
    Rieber EE, Jaffé ER.
    Blood; 1970 Feb 08; 35(2):166-72. PubMed ID: 5414698
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  • 8. [Hereditary erythroenzymopathies. I. Biochemical and genetic aspects].
    Vaca G, Velázquez AL, Cantú JM.
    Bol Oficina Sanit Panam; 1984 Sep 08; 97(3):225-39. PubMed ID: 6239628
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  • 9. Decay of a specific NADP(H)-binding protein during aging of normal and glucose 6-phosphate dehydrogenase-deficient erythrocytes.
    De Flora A, Morelli A, Benatti U, Frascio M, Gaetani GF.
    FEBS Lett; 1977 Oct 15; 82(2):223-6. PubMed ID: 21101
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  • 10. [Oxygenation curves in enzymopathic hemolytic anemias].
    Rotrekl B, Prokopová M.
    Acta Univ Palacki Olomuc Fac Med; 1984 Oct 15; 106():123-31. PubMed ID: 6242617
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  • 11. Effect of haemolysis on the hexose monophosphate pathway in normal and in glucose-6-phosphate dehydrogenase-deficient erythrocytes.
    Galiano S, Mareni C, Gaetani GF.
    Biochim Biophys Acta; 1978 Jan 11; 501(1):1-9. PubMed ID: 23153
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  • 12. Red cell NADP+ and NADPH in glucose-6-phosphate dehydrogenase deficiency.
    Kirkman HN, Gaetani GD, Clemons EH, Mareni C.
    J Clin Invest; 1975 Apr 11; 55(4):875-8. PubMed ID: 235564
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  • 20. Redox and energetic state of red blood cells in G6PD deficiency, heterozygous beta-thalassemia and the combination of both.
    Magnani M, Stocchi V, Canestrari F, Cucchiarini L, Stocchi O, Coppa GV, Felici L, Giorgi PL, Fornaini G.
    Acta Haematol; 1986 Apr 11; 75(4):211-4. PubMed ID: 3096052
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