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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

166 related items for PubMed ID: 6620333

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  • 2. [Cyanosis as a result of drug-induced methemoglobinemia. A case report].
    Hess W, Eberlein HJ, Pöthe H.
    Anaesthesist; 1983 Mar; 32(3):124-6. PubMed ID: 6859496
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  • 3. Methaemoglobinaemia produced by phenazopyridine (Pyridium) in a man with chronic obstructive airways disease.
    Chakraborty TK, Filshie RJ, Lee MR.
    Scott Med J; 1987 Dec; 32(6):185-6. PubMed ID: 3449947
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  • 5. Alteration of NADH-diaphorase and cytochrome b5 reductase activities of erythrocytes, platelets, and leucocytes in hereditary methaemoglobinaemia with and without mental retardation.
    Takeshita M, Matsuki T, Tanishima K, Yubisui T, Yoneyama Y, Kurata K, Hara N, Igarashi T.
    J Med Genet; 1982 Jun; 19(3):204-9. PubMed ID: 6896729
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  • 6. Analyis of met-form haemoglobins in human erythrocytes of normal adults and of a patient with hereditary methaemoglobinaemia due to deficiency of NADH-cytochrome b5 reductase.
    Tomoda A, Imoto M, Hirano M, Yoneyama Y.
    Biochem J; 1979 Aug 01; 181(2):505-7. PubMed ID: 496898
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  • 12. Phenazopyridine-induced methemoglobinemia.
    Terrell JR, Spruill WJ, Parish RC, Jenkins FH.
    Drug Intell Clin Pharm; 1988 Nov 01; 22(11):915. PubMed ID: 3234262
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  • 13. [An infant with hereditary methemoglobinemia].
    Golterman LK, Maaswinkel-Mooy PD.
    Tijdschr Kindergeneeskd; 1989 Apr 01; 57(2):60-2. PubMed ID: 2741161
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  • 14. Metoclopramide-induced methemoglobinemia in a patient with co-existing deficiency of glucose-6-phosphate dehydrogenase and NADH-cytochrome b5 reductase: failure of methylene blue treatment.
    Karadsheh NS, Shaker Q, Ratroat B.
    Haematologica; 2001 Jun 01; 86(6):659-60. PubMed ID: 11418378
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  • 17. 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 01; 66(6):1288-91. PubMed ID: 4063522
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  • 20. 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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