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Journal Abstract Search

159 related items for PubMed ID: 269730

  • 21. Phosphorylation of McArdle phosphorylase induces activity.
    Cerri CG, Willner JH.
    Proc Natl Acad Sci U S A; 1981 May; 78(5):2688-92. PubMed ID: 6265901
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  • 22. Histochemical phosphorylase activity in regenerating muscle fibers from myophosphorylase-deficient patients.
    Roelofs RI, Engel WK, Chauvin PB.
    Science; 1972 Sep 01; 177(4051):795-7. PubMed ID: 4506147
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  • 23. McArdle's syndrome. Fine structural changes in muscle.
    Korényi-Both A, Smith BH, Baruah JK.
    Acta Neuropathol; 1977 Sep 26; 40(1):11-9. PubMed ID: 269622
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  • 24. Expression of glycogen phosphorylase isoforms in cultured muscle from patients with McArdle's disease carrying the p.R771PfsX33 PYGM mutation.
    Nogales-Gadea G, Mormeneo E, García-Consuegra I, Rubio JC, Orozco A, Arenas J, Martín MA, Lucia A, Gómez-Foix AM, Martí R, Andreu AL.
    PLoS One; 2010 Oct 05; 5(10):. PubMed ID: 20957198
    [Abstract] [Full Text] [Related]

  • 25. Angina in McArdle's disease.
    Nicholls DP, Campbell NP, Stevenson HP, Patterson VH.
    Heart; 1996 Oct 05; 76(4):372-3. PubMed ID: 8983689
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  • 26. Increased muscular beta-hydroxyacyl CoA dehydrogenase with McArdle's disease.
    Turk WR, Heller SL, Norris BJ, Nemeth PM.
    Muscle Nerve; 1990 Jul 05; 13(7):607-12. PubMed ID: 2388659
    [Abstract] [Full Text] [Related]

  • 27. Low muscle levels of pyridoxine in McArdle's syndrome.
    Haller RG, Dempsey WB, Feit H, Cook JD, Knochel JP.
    Am J Med; 1983 Feb 05; 74(2):217-20. PubMed ID: 6572033
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  • 28. McArdle's disease in two generations: autosomal recessive transmission with manifesting heterozygote.
    Schmidt B, Servidei S, Gabbai AA, Silva AC, de Sousa Bulle de Oliveira A, DiMauro S.
    Neurology; 1987 Sep 05; 37(9):1558-61. PubMed ID: 3476861
    [Abstract] [Full Text] [Related]

  • 29. 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 05; 47(2):107-15. PubMed ID: 6576726
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  • 34. A new variant of late-onset myophosphorylase deficiency.
    Kost GJ, Verity MA.
    Muscle Nerve; 1980 May 05; 3(3):195-201. PubMed ID: 6929403
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  • 35. McArdle's disease: a rare frameshift mutation in exon 1 of the muscle glycogen phosphorylase gene.
    Bartram C, Edwards RH, Clague J, Beynon RJ.
    Biochim Biophys Acta; 1994 Jul 18; 1226(3):341-3. PubMed ID: 8054367
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  • 37. McArdle's disease in an elderly woman.
    Harris RA, Dowben RM.
    South Med J; 1985 Feb 18; 78(2):191-3. PubMed ID: 3856326
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  • 39. Congenital myopathy due to phosphorylase deficiency.
    Cornelio F, Bresolin N, DiMauro S, Mora M, Balestrini MR.
    Neurology; 1983 Oct 18; 33(10):1383-5. PubMed ID: 6577313
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