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Journal Abstract Search

137 related items for PubMed ID: 5243846

  • 1. McArdle's disease: lack of muscle phosphorylase.
    Dawson DM, Spong FL, Harrington JF.
    Ann Intern Med; 1968 Aug; 69(2):229-35. PubMed ID: 5243846
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  • 3. 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; 37(9):1558-61. PubMed ID: 3476861
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  • 4. 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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  • 6. Acute renal failure in McArdle's disease. Report of two cases.
    Grünfeld JP, Ganeval D, Chanard J, Fardeau M, Dreyfus JC.
    N Engl J Med; 1972 Jun 08; 286(23):1237-41. PubMed ID: 4502558
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  • 8. Metabolic adaptation in muscle of phosphorylase deficiency (McArdle's disease)?
    Nolte J, Schollmeyer P.
    Klin Wochenschr; 1973 Mar 01; 51(5):250-1. PubMed ID: 4511939
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  • 10. Myopathy resembling McArdle's syndrome.
    Slotwiner P, Song SK, Maker HS.
    Arch Neurol; 1969 Jun 01; 20(6):586-98. PubMed ID: 5253619
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  • 18. [McArdle's disease (muscular phosphorylase deficiency)].
    Schollmeyer P, Nolte J, Meisel D, Dichgans J, Jerusalem F.
    Verh Dtsch Ges Inn Med; 1969 Jun 01; 83():1277-80. PubMed ID: 274025
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  • 19. 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 01; 79(1):275-81. PubMed ID: 3466902
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