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Journal Abstract Search

208 related items for PubMed ID: 15603910

  • 1. Disorders of oxidised haemoglobin.
    Percy MJ, McFerran NV, Lappin TR.
    Blood Rev; 2005 Mar; 19(2):61-8. PubMed ID: 15603910
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  • 2. Occupational methaemoglobinaemia. Mechanisms of production, features, diagnosis and management including the use of methylene blue.
    Bradberry SM.
    Toxicol Rev; 2003 Mar; 22(1):13-27. PubMed ID: 14579544
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  • 3. Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families.
    Kedar PS, Colah RB, Ghosh K, Mohanty D.
    Haematologia (Budap); 2002 Mar; 32(4):543-9. PubMed ID: 12803131
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  • 5. Drug- and chemical-induced methaemoglobinaemia. Clinical features and management.
    Hall AH, Kulig KW, Rumack BH.
    Med Toxicol; 1986 Mar; 1(4):253-60. PubMed ID: 3537620
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  • 7. Congenital enzymopenic methaemoglobinaemia.
    Kueh YK, Chio LF, Guan R.
    Ann Acad Med Singap; 1986 Apr; 15(2):250-4. PubMed ID: 3752898
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  • 8. [Methemoglobinemia; a description of a case of NADH methemoglobulin reductase deficiency].
    Gerli GC, Beretta L, Bianchi M, Bernasconi C, Morandi M, Adami R, Ferrari A.
    Minerva Med; 1981 Jul 31; 72(29):1925-30. PubMed ID: 7254639
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  • 9. A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia.
    Kedar PS, Warang P, Nadkarni AH, Colah RB, Ghosh K.
    Blood Cells Mol Dis; 2008 Jul 31; 40(3):323-7. PubMed ID: 17964195
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  • 11. Congenital methaemoglobinaemia in a 61-year-old patient with normal haemoglobin levels.
    de Geus KF, Anas AA, Franssen R, Duijkers FAM, Bikker H, Linthorst GE.
    Neth J Med; 2018 May 31; 76(4):194-197. PubMed ID: 29845943
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  • 13. A novel L218P mutation in NADH-cytochrome b5 reductase associated with type I recessive congenital methemoglobinemia.
    Arikoglu T, Yarali N, Kara A, Bay A, Bozkaya IO, Tunc B, Percy MJ.
    Pediatr Hematol Oncol; 2009 May 31; 26(5):381-5. PubMed ID: 19579085
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  • 17. Congenital methaemoglobinaemia: a rare cause of cyanosis in an adult patient.
    Londhey V, Khadilkar K, Gad J, Chawla B, Asgaonkar D.
    J Assoc Physicians India; 2014 Mar 31; 62(3):269-71. PubMed ID: 25327075
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  • 19. Congenital methaemoglobinaemia Type I in a Turkish infant due to a novel mutation, Pro144Ser, in NADH-cytochrome b5 reductase.
    Percy MJ, Oren H, Savage G, Irken G.
    Hematol J; 2004 Mar 31; 5(4):367-70. PubMed ID: 15297856
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  • 20. [Congenital methaemoglobinaemia--a rare cause of dyspnoea and cyanosis].
    Rasmussen KB, Gantzhorn EK.
    Ugeskr Laeger; 2011 Aug 29; 173(35):2133-4. PubMed ID: 21884667
    [Abstract] [Full Text] [Related]

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