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Journal Abstract Search

212 related items for PubMed ID: 4524323

  • 1. Biochemical determinations in a recently investigated case of McArdle's disease.
    Luca N, Bănileanu S.
    Eur Neurol; 1974; 11(1):58-68. PubMed ID: 4524323
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  • 4. Myophosphorylase deficiency (McArdle's disease) in two interrelated families.
    Cochrane P, Hughes RR, Buxton PH, Yorke RA.
    J Neurol Neurosurg Psychiatry; 1973 Apr; 36(2):217-24. PubMed ID: 4513544
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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. [Apropos of a further case of absence of phosphorylase in the striated muscle (McArdle's disease)].
    Delwaide PJ, Reznik M, Lemaire R, Lelièvre P, Bonnet F.
    Rev Neurol (Paris); 1967 Feb; 116(2):119-40. PubMed ID: 5230980
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  • 11. McArdle's disease. Metabolic studies in a patient and review of the syndrome.
    Fattah SM, Rubulis A, Faloon WW.
    Am J Med; 1970 Jun; 48(6):693-9. PubMed ID: 5268114
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  • 13. Amino acid metabolism during exercise in McArdle's syndrome: evidence of altered alanine metabolism.
    Felig P, Havel RJ, Jorfeldt L, Pernow B, Saltin B, Wahren J.
    J Physiol; 1972 Dec; 227(2):33P-35P. PubMed ID: 4509618
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  • 15. Glucose arteriovenous differences across muscle in McArdle's disease.
    Turner CE, Waterhouse C.
    Am J Med Sci; 1973 Feb; 265(2):109-15. PubMed ID: 4513596
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  • 18. Renal failure in McArdle's disease.
    Bank WJ, DiMauro S, Rowland LP.
    N Engl J Med; 1972 Nov 23; 287(21):1102. PubMed ID: 4507439
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