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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

150 related items for PubMed ID: 9590044

  • 41.
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  • 44. Screening for methylmalonic aciduria in Alberta: a voluntary program with particular significance for the Hutterite Brethren.
    Fowlow SB, Holmes TM, Morgan K, Snyder FF.
    Am J Med Genet; 1985 Nov; 22(3):513-9. PubMed ID: 2865895
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  • 49. Varying neurological phenotypes among muto and mut- patients with methylmalonylCoA mutase deficiency.
    Shevell MI, Matiaszuk N, Ledley FD, Rosenblatt DS.
    Am J Med Genet; 1993 Mar 01; 45(5):619-24. PubMed ID: 7681251
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  • 50. Homozygous nonsense mutation in the MCEE gene and siRNA suppression of methylmalonyl-CoA epimerase expression: a novel cause of mild methylmalonic aciduria.
    Dobson CM, Gradinger A, Longo N, Wu X, Leclerc D, Lerner-Ellis J, Lemieux M, Belair C, Watkins D, Rosenblatt DS, Gravel RA.
    Mol Genet Metab; 2006 Aug 01; 88(4):327-33. PubMed ID: 16697227
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  • 52. Methylmalonic acidemia.
    Cohen JJ.
    Kidney Int; 1979 Mar 01; 15(3):311-20. PubMed ID: 41966
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  • 53. Long-term follow-up of 77 patients with isolated methylmalonic acidaemia.
    Baumgarter ER, Viardot C.
    J Inherit Metab Dis; 1995 Mar 01; 18(2):138-42. PubMed ID: 7564229
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  • 55. Renal transplantation in a patient with methylmalonic acidaemia.
    Van Calcar SC, Harding CO, Lyne P, Hogan K, Banerjee R, Sollinger H, Rieselbach RE, Wolff JA.
    J Inherit Metab Dis; 1998 Oct 01; 21(7):729-37. PubMed ID: 9819702
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  • 58. [Methylmalonic acid].
    Tanaka A, Yamaoka S.
    Nihon Rinsho; 2004 Nov 01; 62 Suppl 11():696-9. PubMed ID: 15628513
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  • 60. Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency.
    Luciani A, Schumann A, Berquez M, Chen Z, Nieri D, Failli M, Debaix H, Festa BP, Tokonami N, Raimondi A, Cremonesi A, Carrella D, Forny P, Kölker S, Diomedi Camassei F, Diaz F, Moraes CT, Di Bernardo D, Baumgartner MR, Devuyst O.
    Nat Commun; 2020 Feb 20; 11(1):970. PubMed ID: 32080200
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