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Journal Abstract Search

133 related items for PubMed ID: 2434909

  • 1. [Methemoglobinemia in the newborn and nursing infant. Genetic and acquired forms. Personal case list].
    Centa A, Camera G, Zucchinetti P, Di Pietro P.
    Pathologica; 1985; 77(1052):659-65. PubMed ID: 2434909
    [No Abstract] [Full Text] [Related]

  • 2. Landmark perspective: The legacy of well-water methemoglobinemia.
    Lukens JN.
    JAMA; 1985; 257(20):2793-5. PubMed ID: 3553638
    [No Abstract] [Full Text] [Related]

  • 3. [Methemoglobin formation in a young infant. Drinking water hygiene in Rheinhessen].
    Toussaint W, Selenka F.
    Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):282-4. PubMed ID: 5538129
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  • 5. Generalised deficiency of cytochrome b5 reductase in congenital methaemoglobinaemia with mental retardation.
    Leroux A, Junien C, Kaplan J, Bamberger J.
    Nature; 1975 Dec 18; 258(5536):619-20. PubMed ID: 1207738
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  • 6. [Hereditary methemoglobinemia due to NADH cytochrome b5 abnormality--clinical importance of the enzyme in leukocytes and platelets].
    Tomita Y, Inagaki M, Taki M, Miura T, Saito N, Meguro T, Yamada K, Fujii H, Takizawa T, Miwa S.
    Rinsho Ketsueki; 1986 Mar 18; 27(3):412-9. PubMed ID: 3735692
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  • 8. [Methemoglobinemias. Cytochrome b5-reductase deficiency].
    Thu DT, Damianova L.
    Eksp Med Morfol; 1993 Mar 18; 31(1-2):42-50. PubMed ID: 8258315
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  • 11. Enzymopenic hereditary methemoglobinemia: a clinical/biochemical classification.
    Jaffé ER.
    Blood Cells; 1986 Mar 18; 12(1):81-90. PubMed ID: 3539237
    [Abstract] [Full Text] [Related]

  • 12. [Clinical and biological forms of cytochrome b5 reductase deficiency].
    Kaplan JC, Leroux A, Beauvais P.
    C R Seances Soc Biol Fil; 1979 Mar 18; 173(2):368-79. PubMed ID: 159760
    [Abstract] [Full Text] [Related]

  • 13. Familial idiopathic methemoglobinemia revisited: original cases reveal 2 novel mutations in NADH-cytochrome b5 reductase.
    Percy MJ, Gillespie MJ, Savage G, Hughes AE, McMullin MF, Lappin TR.
    Blood; 2002 Nov 15; 100(10):3447-9. PubMed ID: 12393396
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  • 14. [Prenatal diagnosis of generalized cytochrome b5 reductase deficiency (congenital methemoglobinemia with mental retardation, type II) (author's transl)].
    Kaplan JC, Junien C, Leroux A, Bamberger J, Bakouri S, Boué J, Boué A.
    Ann Med Interne (Paris); 1981 Nov 15; 132(2):93-6. PubMed ID: 7235451
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  • 16. Methemoglobinemia caused by the ingestion of courgette soup given in order to resolve constipation in two formula-fed infants.
    Savino F, Maccario S, Guidi C, Castagno E, Farinasso D, Cresi F, Silvestro L, Mussa GC.
    Ann Nutr Metab; 2006 Nov 15; 50(4):368-71. PubMed ID: 16809905
    [Abstract] [Full Text] [Related]

  • 17. [Genetics and biochemistry of NADH-cytochrome b5 reductase deficiency].
    Shirabe K.
    Nihon Rinsho; 1999 Sep 15; 57 Suppl():769-71. PubMed ID: 10543233
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  • 19. [Gene analysis and genetic diagnosis of hereditary erythrocyte abnormalities. Cytochrome b5 reductase deficiency].
    Yokota E, Naito Y, Niho Y.
    Nihon Rinsho; 1987 Dec 15; 45(12):2911-6. PubMed ID: 3446879
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  • 20. Hereditary methemoglobinemia due to cytochrome b5 reductase deficiency in blood cells without associated neurologic and mental disorders.
    Tanishima K, Tanimoto K, Tomoda A, Mawatari K, Matsukawa S, Yoneyama Y, Ohkuwa H, Takazakura E.
    Blood; 1985 Dec 15; 66(6):1288-91. PubMed ID: 4063522
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