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Journal Abstract Search

146 related items for PubMed ID: 285339

  • 21. 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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  • 24. An automated assay of glycogen phosphorylase in the direction of phosphorolysis.
    Schreiber WE, Bowling S.
    Ann Clin Biochem; 1990 Mar; 27 ( Pt 2)():129-32. PubMed ID: 2109566
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  • 28. McArdle's syndrome. Fine structural changes in muscle.
    Korényi-Both A, Smith BH, Baruah JK.
    Acta Neuropathol; 1977 Sep 26; 40(1):11-9. PubMed ID: 269622
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  • 31. Absence of biochemical heterogeneity in McArdle's disease. A high resolution SDS-polyacrylamide gel electrophoresis study.
    Mantle D, Lauffart B, Atack J, Lane RJ.
    J Neurol Sci; 1987 Mar 26; 78(1):63-70. PubMed ID: 3471865
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  • 35. McArdle disease: molecular genetic update.
    Andreu AL, Nogales-Gadea G, Cassandrini D, Arenas J, Bruno C.
    Acta Myol; 2007 Jul 26; 26(1):53-7. PubMed ID: 17915571
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  • 36. Phenotype consequences of myophosphorylase dysfunction: insights from the McArdle mouse model.
    Brull A, de Luna N, Blanco-Grau A, Lucia A, Martin MA, Arenas J, Martí R, Andreu AL, Pinós T.
    J Physiol; 2015 Jun 15; 593(12):2693-706. PubMed ID: 25873271
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  • 37. Muscle diffusion tensor imaging in glycogen storage disease V (McArdle disease).
    Rehmann R, Schlaffke L, Froeling M, Kley RA, Kühnle E, De Marées M, Forsting J, Rohm M, Tegenthoff M, Schmidt-Wilcke T, Vorgerd M.
    Eur Radiol; 2019 Jun 15; 29(6):3224-3232. PubMed ID: 30560358
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