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Journal Abstract Search

147 related items for PubMed ID: 14272202

  • 1. MCARDLE'S DISEASE: HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE.
    FAHN S, SCHOTLAND DL, ROWLAND LP.
    Trans Am Neurol Assoc; 1963; 88():145-7. PubMed ID: 14272202
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  • 4. MUSCLE PHOSPHORYLASE DEFICIENCY.
    SHY GM.
    Ann Intern Med; 1965 Feb; 62():409-11. PubMed ID: 14259223
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  • 5. MCARDLE'S SYNDROME WITH PREVIOUSLY UNREPORTED ELECTROCARDIOGRAPHIC AND SERUM ENZYME ABNORMALITIES.
    RATINOV G, BAKER WP, SWAIMAN KF.
    Ann Intern Med; 1965 Feb; 62():328-34. PubMed ID: 14259215
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  • 7. Molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). RNA and DNA analysis.
    Gautron S, Daegelen D, Mennecier F, Dubocq D, Kahn A, Dreyfus JC.
    J Clin Invest; 1987 Jan; 79(1):275-81. PubMed ID: 3466902
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  • 10. The clinical diagnosis of McArdle's disease. Identification of another family with deficiency of muscle phosphorylase.
    Rowland LP, Lovelace RE, Schotland DL, Araki S, Carmel P.
    Neurology; 1966 Jan; 16(1):93-100. PubMed ID: 5215287
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  • 13. McArdle's disease: a clinical review and case report.
    Keel BR, Brit M.
    Tenn Med; 2013 Jan; 106(10):33, 37. PubMed ID: 24282836
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  • 14. [McArdle's disease without typical symptoms].
    Watanabe M, Matsubara E, Amari M, Okamoto K, Hirai S.
    Rinsho Shinkeigaku; 1990 Nov; 30(11):1247-51. PubMed ID: 2085931
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  • 17. McArdle's syndrome: phosphorylase-deficient myopathy.
    MELLICK RS, MAHLER RF, HUGHES BP.
    Lancet; 1962 May 19; 1(7238):1045-8. PubMed ID: 14472393
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  • 19. Myopathy in McArdle's syndrome. Improvement with a high-protein diet.
    Slonim AE, Goans PJ.
    N Engl J Med; 1985 Feb 07; 312(6):355-9. PubMed ID: 3855499
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