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Journal Abstract Search

114 related items for PubMed ID: 6294950

  • 21.
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  • 23. Gentamicin treatment in McArdle disease: failure to correct myophosphorylase deficiency.
    Schroers A, Kley RA, Stachon A, Horvath R, Lochmüller H, Zange J, Vorgerd M.
    Neurology; 2006 Jan 24; 66(2):285-6. PubMed ID: 16434679
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  • 24. Metabolic basis of improved exercise tolerance: muscle phosphorylase deficiency after glucagon administration.
    Kono N, Mineo I, Sumi S, Shimizu T, Kang J, Nonaka K, Tarui S.
    Neurology; 1984 Nov 24; 34(11):1471-6. PubMed ID: 6593602
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  • 25. Adenovirus-mediated delivery into myocytes of muscle glycogen phosphorylase, the enzyme deficient in patients with glycogen-storage disease type V.
    Baqué S, Newgard CB, Gerard RD, Guinovart JJ, Gómez-Foix AM.
    Biochem J; 1994 Dec 15; 304 ( Pt 3)(Pt 3):1009-14. PubMed ID: 7818463
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  • 27. An A-to-C substitution involving the translation initiation codon in a patient with myophosphorylase deficiency (McArdle's disease).
    Tsujino S, Rubin LA, Shanske S, DiMauro S.
    Hum Mutat; 1994 Dec 15; 4(1):73-5. PubMed ID: 7951262
    [No Abstract] [Full Text] [Related]

  • 28. Absence of functional messenger RNA for glycogen phosphorylase in the muscle of two patients with McArdle's disease.
    Daegelen D, Munnich A, Levin MJ, Girault A, Goasguen J, Kahn A, Dreyfus JC.
    Ann Hum Genet; 1983 May 15; 47(2):107-15. PubMed ID: 6576726
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  • 29. Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease.
    Howell JM, Walker KR, Creed KE, Dunton E, Davies L, Quinlivan R, Karpati G.
    Neuromuscul Disord; 2014 Feb 15; 24(2):167-77. PubMed ID: 24309536
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  • 30. Vascular insufficiency in McArdle's disease.
    Wheeler SD, Brooke MH.
    Neurology; 1983 Feb 15; 33(2):249-50. PubMed ID: 6571954
    [No Abstract] [Full Text] [Related]

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  • 33. A metabolic myopathy due to absence of muscle phosphorylase.
    PEARSON CM, RIMER DG, MOMMAERTS WF.
    Am J Med; 1961 Apr 15; 30():502-17. PubMed ID: 13733779
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  • 34.
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  • 35. Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease.
    Garcia-Consuegra I, Rubio JC, Nogales-Gadea G, Bautista J, Jiménez S, Cabello A, Lucía A, Andreu AL, Arenas J, Martin MA.
    Hum Genet; 2009 Apr 15; 125(3):343. PubMed ID: 19320016
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  • 36.
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  • 37. Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease.
    Viéitez I, Teijeira S, Otolano S, Parente P, San Millán B, Navarro C.
    Hum Genet; 2009 Apr 15; 125(3):351. PubMed ID: 19320039
    [No Abstract] [Full Text] [Related]

  • 38. Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease.
    Viéitez I, Teijeira S, San Millán B, Navarro C.
    Hum Genet; 2009 Apr 15; 125(3):339. PubMed ID: 19309804
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  • 39. Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease.
    Viéitez I, Teijeira S, Millán BS, Navarro C.
    Hum Genet; 2009 Apr 15; 125(3):335. PubMed ID: 19309779
    [No Abstract] [Full Text] [Related]

  • 40. Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease.
    Viéitez I, Teijeira S, San Millán B, Navarro C.
    Hum Genet; 2009 Apr 15; 125(3):349. PubMed ID: 19320035
    [No Abstract] [Full Text] [Related]

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