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PUBMED FOR HANDHELDS

Journal Abstract Search


247 related items for PubMed ID: 5543874

  • 1. Electrophoretic and functional variants of NADH-methemoglobin reductase in hereditary methemoglobinemia.
    Hsieh HS, Jaffé ER.
    J Clin Invest; 1971 Jan; 50(1):196-202. PubMed ID: 5543874
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  • 2. Unstable variant of NADH methemoglobin reductase in Puerto Ricans with hereditary methemoglobinemia.
    Schwartz JM, Paress PS, Ross JM, DiPillo F, Rizek R.
    J Clin Invest; 1972 Jun; 51(6):1594-601. PubMed ID: 4336945
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  • 3. Concentration of NADH-cytochrome b5 reductase in erythrocytes of normal and methemoglobinemic individuals measured with a quantitative radioimmunoblotting assay.
    Borgese N, Pietrini G, Gaetani S.
    J Clin Invest; 1987 Nov; 80(5):1296-302. PubMed ID: 3680497
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  • 4. Methemoglobin pathophysiology.
    Jaffé ER.
    Prog Clin Biol Res; 1981 Nov; 51():133-51. PubMed ID: 7022466
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  • 5. Enzymopenic hereditary methemoglobinemia.
    Jaffé ER.
    Haematologia (Budap); 1982 Dec; 15(4):389-99. PubMed ID: 6764628
    [Abstract] [Full Text] [Related]

  • 6. Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families.
    Kedar PS, Colah RB, Ghosh K, Mohanty D.
    Haematologia (Budap); 2002 Dec; 32(4):543-9. PubMed ID: 12803131
    [Abstract] [Full Text] [Related]

  • 7. [Cyanosis in children caused by inherited methemoglobinemia due to deficiency of NADH-dependent methemoglobin reductase in erythrocytes].
    Jabłońska-Skwiecińska E, Wierzbicka M, Kubicka K.
    Pediatr Pol; 1989 Jan; 64(1):53-9. PubMed ID: 2812907
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  • 8. Recessive hereditary methemoglobinemia: two novel mutations in the NADH-cytochrome b5 reductase gene.
    Fermo E, Bianchi P, Vercellati C, Marcello AP, Garatti M, Marangoni O, Barcellini W, Zanella A.
    Blood Cells Mol Dis; 2008 Jan; 41(1):50-5. PubMed ID: 18343696
    [Abstract] [Full Text] [Related]

  • 9. NADH-methemoglobin reductase and methemoglobinemia among leprosy patients.
    Magna LA, Beiguelman B.
    Int J Lepr Other Mycobact Dis; 1984 Dec; 52(4):475-81. PubMed ID: 6535820
    [Abstract] [Full Text] [Related]

  • 10. Membrane-bound cytochrome b5 reductase (methemoglobin reductase) in human erythrocytes. Study in normal and methemoglobinemic subjects.
    Choury D, Leroux A, Kaplan JC.
    J Clin Invest; 1981 Jan; 67(1):149-55. PubMed ID: 7451647
    [Abstract] [Full Text] [Related]

  • 11. Generalized deficiency of the NADH-methemoglobin reductase in congenital methemoglobinemia with neurological symptoms.
    Jabłońska-Skwiecińska E, Holtorp-Tyszkiewiczowa J, Staniszewska K.
    Biomed Biochim Acta; 1984 Jan; 43(6):S98-100. PubMed ID: 6487287
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  • 12. 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 Jan; 59(6):348-53. PubMed ID: 97893
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