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Journal Abstract Search

117 related items for PubMed ID: 6577313

  • 1. Congenital myopathy due to phosphorylase deficiency.
    Cornelio F, Bresolin N, DiMauro S, Mora M, Balestrini MR.
    Neurology; 1983 Oct; 33(10):1383-5. PubMed ID: 6577313
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  • 2. McArdle's disease: a study on the molecular basis of two different etiologies of myophosphorylase deficiency.
    Koster JF, Slee RG, Jennekens FG, Wintzen AR, van Berkel TJ.
    Clin Chim Acta; 1979 Jun 15; 94(3):229-35. PubMed ID: 111879
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  • 4. Phosphorylase isoenzymes in normal and myophosphorylase-deficient human heart.
    Miranda AF, Nette EG, Hartlage PL, DiMauro S.
    Neurology; 1979 Nov 15; 29(11):1538-41. PubMed ID: 291791
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  • 7. Phosphorylation of McArdle phosphorylase induces activity.
    Cerri CG, Willner JH.
    Proc Natl Acad Sci U S A; 1981 May 15; 78(5):2688-92. PubMed ID: 6265901
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  • 8. McArdle's disease--what limit to the age of onset?
    Hewlett RH, Gardner-Thorpe C.
    S Afr Med J; 1978 Jan 14; 53(2):60-3. PubMed ID: 273990
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  • 11. In McArdle disease, phosphorylase deficiency is the tip of an iceberg.
    Willner JH, Cerri CG, Wood DS, Ponzetto-Zimmerman C, Reydel PM.
    Trans Am Neurol Assoc; 1981 Jan 14; 106():208-9. PubMed ID: 6294950
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  • 12. Research on molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). Use of new protein mapping and immunological techniques.
    Daegelen-Proux D, Kahn A, Marie J, Dreyfus JC.
    Ann Hum Genet; 1981 May 14; 45(2):113-20. PubMed ID: 6797345
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  • 13. McArdle disease: phosphorylase activity in regenerating muscle fibers.
    Mitsumoto H.
    Neurology; 1979 Feb 14; 29(2):258-62. PubMed ID: 285339
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  • 18. McArdle disease: the mysterious appearance of phosphorylase activity in cells that ought to lack the genetic program. A fetal isoenzyme?
    DiMauro S, Arnold S, Miranda A, Rowland LP.
    Trans Am Neurol Assoc; 1977 Feb 14; 102():112-5. PubMed ID: 278321
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