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Journal Abstract Search

157 related items for PubMed ID: 4292867

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  • 24. Activity of NADH- and NADPH-dependent methemoglobin reductases in erythrocytes from fetal to adult age. A parallel assessment.
    Vetrella M, Astedt B, Barthelmai W, Neuvians D.
    Klin Wochenschr; 1971 Sep 01; 49(17):972-7. PubMed ID: 4398423
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  • 28. [Various enzymatic aspects of erythrocyte glycolytic metabolism in hereditary methemoglobinemia. Changes in relation to treatment with ascorbic acid].
    Esposito L, Ferrara M, Tomasi L, De Filippo P.
    Pediatria (Napoli); 1977 Sep 30; 85(3):474-81. PubMed ID: 593782
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  • 33. An enzyme variation in a case of congenital methemoglobinemia.
    Gotlieb A, Nordan UZ, Hegesh E.
    Isr J Med Sci; 1973 Jul 30; 9(7):909-13. PubMed ID: 4354625
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  • 35. Congenital methemoglobin-reductase (cytochrome b5 reductase) deficiency associated with mental retardation in a Spanish girl.
    Vives-Corrons JL, Pujades A, Vela E, Corretger JM, Leroux A, Kaplan JC.
    Acta Haematol; 1978 Jul 30; 59(6):348-53. PubMed ID: 97893
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  • 36. Hereditary methaemoglobinaemia due to enzyme deficiency: a case report and study of a Chatham Island family.
    Watt MW, Taylor IM.
    N Z Med J; 1973 Oct 24; 78(501):354-5. PubMed ID: 4519433
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  • 37. [Congenital methemoglobinemia caused by the NADH-diaphorase deficiency].
    Stanulović M, Mijatović B, Marković O.
    Med Pregl; 1971 Oct 24; 24(9):463-7. PubMed ID: 4333391
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  • 38. [The enzyme defect in recessive congenital methemoglobinemia with encephalopathy. A new defective variant of NADH-diaphorase (Beni-Messous variant)].
    Kaplan JC, Leroux A, Bakouri S, Grangaud JP, Benabadji M.
    Nouv Rev Fr Hematol; 1974 Oct 24; 14(6):755-70. PubMed ID: 4282504
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