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Journal Abstract Search

168 related items for PubMed ID: 2062570

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  • 4. [McArdle's disease. Apropos of a case].
    Yuste JR, Beloqui O, De la Peña A, Rodríguez-Rosado R, Monreal JI, Prósper F, Prieto J.
    Rev Med Univ Navarra; 1998; 42(1):29-33. PubMed ID: 10420954
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  • 5. HyperCKemia as the only sign of McArdle's disease in a child.
    Bruno C, Bertini E, Santorelli FM, DiMauro S.
    J Child Neurol; 2000 Feb; 15(2):137-8. PubMed ID: 10695902
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  • 12. McArdle's disease: molecular genetics and metabolic consequences of the phenotype.
    Beynon RJ, Bartram C, Hopkins P, Toescu V, Gibson H, Phoenix J, Edwards RH.
    Muscle Nerve Suppl; 1995 Feb; 3():S18-22. PubMed ID: 7603521
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  • 14. Myophosphorylase deficiency impairs muscle oxidative metabolism.
    Haller RG, Lewis SF, Cook JD, Blomqvist CG.
    Ann Neurol; 1985 Feb; 17(2):196-9. PubMed ID: 3856415
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  • 16. Absence of functional messenger RNA for glycogen phosphorylase in the muscle of two patients with McArdle's disease.
    Daegelen D, Munnich A, Levin MJ, Girault A, Goasguen J, Kahn A, Dreyfus JC.
    Ann Hum Genet; 1983 May; 47(2):107-15. PubMed ID: 6576726
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  • 17. Myophosphorylase deficiency (McArdle's disease): report of a family.
    Mahmud MZ, Howell RR, Stevenson RE, Gilroy J.
    Can J Neurol Sci; 1976 Aug; 3(3):175-9. PubMed ID: 1067141
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  • 19. 31-P NMR characterization of the metabolic anomalies associated with the lack of glycogen phosphorylase activity in human forearm muscle.
    Bendahan D, Confort-Gouny S, Kozak-Ribbens G, Cozzone PJ.
    Biochem Biophys Res Commun; 1992 May 29; 185(1):16-21. PubMed ID: 1599452
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  • 20. 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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