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PUBMED FOR HANDHELDS

Journal Abstract Search


153 related items for PubMed ID: 5404915

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  • 22. [Familial methemoglobinemia due to diaphorase deficiency: a 3d Swiss line].
    Marti HR, Dorta T, Deubelbeiss KA.
    Schweiz Med Wochenschr; 1966 Mar 19; 96(11):355-7. PubMed ID: 5987762
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  • 30. [Inborn methemoglobinemia].
    Benedeková M, Benko J, Bircák J, Gvozdjaková G, Klimentová T, Sakalová A, Vrsanská V.
    Cesk Pediatr; 1978 Jun 19; 33(6):342-5. PubMed ID: 688508
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  • 31. [Erythrocyte metabolism and oxygen transport].
    Kaplan JC.
    Schweiz Med Wochenschr; 1971 Dec 11; 101(49):1751-4. PubMed ID: 5140909
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  • 37. Congenital methemoglobinemia methemoglobin reductase deficiency.
    Koepke JA.
    Ann Clin Lab Sci (1971); 1971 Dec 11; 1(3):222-6. PubMed ID: 5154970
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  • 39. NADH diaphorase: an inherited variant associated with normal methemoglobin reduction.
    Detter JC, Anderson JE, Giblett ER.
    Am J Hum Genet; 1970 Jan 11; 22(1):100-4. PubMed ID: 5411644
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  • 40. Diaphorase deficiency methaemoglobinaemia mimicking cardiac disease in pregnancy.
    Vassallo L, Cauchi M.
    J Obstet Gynaecol Br Commonw; 1970 Feb 11; 77(2):178-9. PubMed ID: 5419883
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