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Journal Abstract Search

269 related items for PubMed ID: 11594178

  • 1. [McArdle disease: report of four brothers with myophosphorylase deficiency].
    López Martín A, Baños Madrid RI, García-Estañ Candela J, García Pérez B, Pérez Bautista FJ, Salmerón P.
    An Med Interna; 2001 Mar; 18(3):136-8. PubMed ID: 11594178
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  • 2. McArdle disease in a Druze family.
    Sarova-Pinhas I, Sadeh M.
    Isr J Med Sci; 1989 Feb; 25(2):64-8. PubMed ID: 2703328
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  • 3. [McArdle disease: differential diagnosis of the increase in creatine kinase induced by the exercise test].
    Frick E, Reutter FW, Weder B.
    Schweiz Med Wochenschr; 1988 Dec 31; 118(52):1993-6. PubMed ID: 3217781
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  • 4. Molecular diagnosis of McArdle disease: revised genomic structure of the myophosphorylase gene and identification of a novel mutation.
    Kubisch C, Wicklein EM, Jentsch TJ.
    Hum Mutat; 1998 Dec 31; 12(1):27-32. PubMed ID: 9633816
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  • 8. Splice mutations preserve myophosphorylase activity that ameliorates the phenotype in McArdle disease.
    Vissing J, Duno M, Schwartz M, Haller RG.
    Brain; 2009 Jun 31; 132(Pt 6):1545-52. PubMed ID: 19433441
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  • 13. [Myalgia during warming-up in a 12-year-old boy].
    Koenraads M, den Boer JA, Kerkhoff H, Sas TC.
    Ned Tijdschr Geneeskd; 2011 Jun 31; 155():A2668. PubMed ID: 21527049
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