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Journal Abstract Search

74 related items for PubMed ID: 2161189

  • 1.
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  • 2. McArdle disease in a Druze family.
    Sarova-Pinhas I, Sadeh M.
    Isr J Med Sci; 1989 Feb; 25(2):64-8. PubMed ID: 2703328
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  • 4. [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 Feb; 65(5):550-4. PubMed ID: 17913675
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  • 5. [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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  • 7. [McArdle disease (gycogenosis type V): analysis of clinical, biological and genetic features of five French patients].
    Delmont E, Sacconi S, Berge-Lefranc JL, Aquaron R, Butori C, Desnuelle C.
    Rev Neurol (Paris); 2008 Nov 31; 164(11):912-6. PubMed ID: 18808785
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  • 8. [Exercise-induced muscular weakness, myalgia and contractures. I. A clinical review].
    Mattle H, Jerusalem F.
    Schweiz Med Wochenschr; 1977 Apr 02; 107(13):428-36. PubMed ID: 139680
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  • 9. [McArdle's disease in a 14-year-old girl with fatigability and raised muscle enzymes].
    López-Pisón J, Muñoz-Albillos MS, Boudet-García A, Giménez-Más JA, Peña-Segura JL, Abenia-Usón P.
    Rev Neurol; 1977 Apr 02; 30(10):932-4. PubMed ID: 10919189
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  • 10. Splice mutations preserve myophosphorylase activity that ameliorates the phenotype in McArdle disease.
    Vissing J, Duno M, Schwartz M, Haller RG.
    Brain; 2009 Jun 02; 132(Pt 6):1545-52. PubMed ID: 19433441
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  • 12. In McArdle disease, phosphorylase deficiency is the tip of an iceberg.
    Willner JH, Cerri CG, Wood DS, Ponzetto-Zimmerman C, Reydel PM.
    Trans Am Neurol Assoc; 1981 Jun 02; 106():208-9. PubMed ID: 6294950
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  • 13. Permanent muscle weakness in McArdle disease.
    Nadaj-Pakleza AA, Vincitorio CM, Laforêt P, Eymard B, Dion E, Teijeira S, Vietez I, Jeanpierre M, Navarro C, Stojkovic T.
    Muscle Nerve; 2009 Sep 02; 40(3):350-7. PubMed ID: 19670320
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  • 17. [Myoadenylate deaminase deficiency in a child with myalgias induced by physical exercise].
    Pantoja-Martínez J, Navarro Fernández-Balbuena C, Gormaz-Moreno M, Quintans-Castro B, Esparza-Sánchez MA, Bonet-Arzo J.
    Rev Neurol; 2009 Sep 02; 39(5):431-4. PubMed ID: 15378456
    [Abstract] [Full Text] [Related]

  • 18. One-year follow-up in a child with McArdle disease: exercise is medicine.
    Pérez M, Foster C, González-Freire M, Arenas J, Lucia A.
    Pediatr Neurol; 2008 Feb 02; 38(2):133-6. PubMed ID: 18206796
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  • 19. Adult phosphorylase b kinase deficiency.
    Clemens PR, Yamamoto M, Engel AG.
    Ann Neurol; 1990 Oct 02; 28(4):529-38. PubMed ID: 2252364
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  • 20. McArdle disease: the mystery of reappearing phosphorylase activity in muscle culture--a fetal isoenzyme.
    DiMauro S, Arnold S, Miranda A, Rowland LP.
    Ann Neurol; 1978 Jan 02; 3(1):60-6. PubMed ID: 418736
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