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236 related items for PubMed ID: 10695902

  • 1. 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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  • 2. [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 Feb; 42(1):29-33. PubMed ID: 10420954
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  • 3. [McArdle's disease without typical symptoms].
    Watanabe M, Matsubara E, Amari M, Okamoto K, Hirai S.
    Rinsho Shinkeigaku; 1990 Nov; 30(11):1247-51. PubMed ID: 2085931
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  • 4. McArdle's disease with late-onset symptoms: case report and review of the literature.
    Felice KJ, Schneebaum AB, Jones HR.
    J Neurol Neurosurg Psychiatry; 1992 May; 55(5):407-8. PubMed ID: 1602316
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  • 10. [McArdle disease: differential diagnosis of the increase in creatine kinase induced by the exercise test].
    Frick E, Reutter FW, Weder B.
    Schweiz Med Wochenschr; 1988 Dec 31; 118(52):1993-6. PubMed ID: 3217781
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  • 11. [Late diagnosis of a McArdle disease's case (type V glycogenosis)].
    Flavier S, Rolland MO, Eude M, Fédou C, Brun JF, Maire I, Mercier J, Raynaud E.
    Ann Biol Clin (Paris); 2007 Dec 31; 65(5):550-4. PubMed ID: 17913675
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  • 12. Mcardle's disease. A case report.
    Dirik E, Taşkin F, Eroğlu Y, Büyükgebiz B, Selamzade M, Cevik NT.
    Turk J Pediatr; 1996 Dec 31; 38(3):355-9. PubMed ID: 8827906
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  • 13. Glycogen storage disease type V (Mc Ardle's disease): a report on three cases.
    Krishnamoorthy N, Santosh V, Yasha TC, Mahadevan A, Shankar SK, Jethwani D, Taly AB, Bhanu K, Gayathri N.
    Neurol India; 2011 Dec 31; 59(6):884-6. PubMed ID: 22234204
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  • 14. McArdle's disease with non-insulin-dependent diabetes mellitus: the beneficial effects of hyperglycemia and hyperinsulinemia for exercise intolerance.
    Yamauchi A, Amano K, Ichikawa Y, Nakamoto S, Takei I, Maruyama H, Kono N, Saruta T.
    Intern Med; 1996 May 31; 35(5):403-6. PubMed ID: 8797056
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  • 16. A homozygous missense mutation (A659D) in the myophosphorylase gene in a Spanish patient with McArdle's disease.
    Martín MA, Rubio JC, Campos Y, Ricoy JR, Cabello A, Arenas J.
    Neuromuscul Disord; 2000 Aug 31; 10(6):447-9. PubMed ID: 10899452
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  • 17. A new stop codon mutation (Y52X) in the myophosphorylase gene in a Greek patient with McArdle's disease.
    Hadjigeorgiou GM, Papadimitriou A, Musumeci O, Paterakis K, Flabouriari K, Shanske S, DiMauro S.
    J Neurol Sci; 2002 Feb 15; 194(1):83-6. PubMed ID: 11809171
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