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Journal Abstract Search

204 related items for PubMed ID: 15045049

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  • 3. 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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  • 7. Unforeseen cardiac involvement in McArdle's disease.
    Moustafa S, Patton DJ, Connelly MS.
    Heart Lung Circ; 2013 Sep; 22(9):769-71. PubMed ID: 23337261
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  • 11. McArdle's disease: a clinical review and case report.
    Keel BR, Brit M.
    Tenn Med; 2013 Sep; 106(10):33, 37. PubMed ID: 24282836
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  • 13. [McArdle's disease: a case report].
    Levy JA, Gagioti SM, Cavalieri MJ, Pereira JR.
    Arq Neuropsiquiatr; 1980 Dec; 38(4):411-4. PubMed ID: 6937160
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  • 16. 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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  • 17. [Muscle phosphorylase deficiency in childhood. A case report].
    Bruno C, Iester A, Bado M, Morreale G, Broda P, Minetti C, Cordone A, Cordone G.
    Minerva Pediatr; 1994 Oct 15; 46(10):459-62. PubMed ID: 7808367
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  • 18. [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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  • 20. 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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