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Journal Abstract Search

285 related items for PubMed ID: 5230980

  • 21.
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  • 23. 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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  • 24.
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  • 25. Neuropathy in McArdle's syndrome.
    Upton AR, McComas AJ, Bianchi FA.
    N Engl J Med; 1973 Oct 04; 289(14):750-1. PubMed ID: 4516762
    [No Abstract] [Full Text] [Related]

  • 26. Variable presentation of the clinical phenotype of McArdle's disease in a kindred harbouring a novel compound genotype in the muscle glycogen phosphorylase gene.
    Paradas C, Fernandez-Cadenas I, Gallardo E, Lligé D, Arenas J, Illa I, Andreu AL.
    Neurosci Lett; 2005 Dec 31; 391(1-2):28-31. PubMed ID: 16154688
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  • 27.
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  • 28. Steroid myopathy complicating McArdle's disease.
    Mastaglia FL, McCollum JP, Larson PF, Hudgson P.
    J Neurol Neurosurg Psychiatry; 1970 Feb 31; 33(1):111-20. PubMed ID: 4313853
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  • 29. [Experimental 2,4-dichlorophenoxyacetate myopathy. I. Electrophysiological and histochemical results].
    Rüdiger KD, Meerbach W, Osske G, Fischer W.
    Zentralbl Allg Pathol; 1972 Feb 31; 115(1):145-52. PubMed ID: 4503486
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  • 33. The value of electron microscopy in muscle biopsies.
    Hudgson P.
    Proc R Soc Med; 1970 May 31; 63(5):470-4. PubMed ID: 5271562
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  • 34. McArdle's disease in the 1980s.
    Layzer RB.
    N Engl J Med; 1985 Feb 07; 312(6):370-1. PubMed ID: 3855500
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  • 35. Contracture in McArdle's disease. Stability of adenosine triphosphate during contracture in phosphorylase-deficient human muscle.
    Rowland LP, Araki S, Carmel P.
    Arch Neurol; 1965 Nov 07; 13(5):541-4. PubMed ID: 5892420
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  • 36. A CASE OF MCARDLE'S SYNDROME WITH A POSITIVE FAMILY HISTORY.
    HOCKADAY TD, DOWNEY JA, MOTTRAM RF.
    J Neurol Neurosurg Psychiatry; 1964 Jun 07; 27(3):186-97. PubMed ID: 14175283
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  • 37. [McArdle's syndrome].
    Lobzin VS, Zagorodnyĭ RI, Glushkov BS.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973 Jun 07; 73(6):820-5. PubMed ID: 4518645
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  • 38. Late-onset Mcardle's disease with unusual electromyographic findings.
    Pourmand R, Sanders DB, Corwin HM.
    Arch Neurol; 1983 Jun 07; 40(6):374-7. PubMed ID: 6573876
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  • 39.
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  • 40. [McArdle's syndrome (myopathy in muscle phosphorylase deficiency)].
    Schimrigk K, Mertens HG, Ricker K, Führ J, Eyer P, Pette D.
    Klin Wochenschr; 1967 Jan 01; 45(1):1-17. PubMed ID: 6031735
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