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Journal Abstract Search

152 related items for PubMed ID: 8983689

  • 21. Myophosphorylase gene transfer in McArdle's disease myoblasts in vitro.
    Pari G, Crerar MM, Nalbantoglu J, Shoubridge E, Jani A, Tsujino S, Shanske S, DiMauro S, Howell JM, Karpati G.
    Neurology; 1999 Oct 12; 53(6):1352-4. PubMed ID: 10522901
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  • 25. The molecular genetic basis of myophosphorylase deficiency (McArdle's disease).
    Tsujino S, Shanske S, Nonaka I, DiMauro S.
    Muscle Nerve Suppl; 1995 Oct 12; 3():S23-7. PubMed ID: 7603523
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  • 28. [McArdle's disease. Apropos of a case].
    Yuste JR, Beloqui O, De la Peña A, Rodríguez-Rosado R, Monreal JI, Prósper F, Prieto J.
    Rev Med Univ Navarra; 1998 Oct 12; 42(1):29-33. PubMed ID: 10420954
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  • 29. Phosphorylase isoenzymes in normal and myophosphorylase-deficient human heart.
    Miranda AF, Nette EG, Hartlage PL, DiMauro S.
    Neurology; 1979 Nov 12; 29(11):1538-41. PubMed ID: 291791
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  • 31. McArdle's disease (myophosphorylase deficiency) presenting as acute renal failure.
    Sidhu N, Thompson T.
    N Z Med J; 2005 Aug 12; 118(1220):U1614. PubMed ID: 16132075
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  • 33. McArdle's disease-muscle glycogen phosphorylase deficiency.
    Bartram C, Edwards RH, Beynon RJ.
    Biochim Biophys Acta; 1995 Aug 15; 1272(1):1-13. PubMed ID: 7662715
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  • 38. Low muscle levels of pyridoxine in McArdle's syndrome.
    Haller RG, Dempsey WB, Feit H, Cook JD, Knochel JP.
    Am J Med; 1983 Feb 15; 74(2):217-20. PubMed ID: 6572033
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