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Journal Abstract Search

646 related items for PubMed ID: 19209654

  • 1. [Diagnosis of a myopathic disease in adult].
    Eymard B.
    Rev Prat; 2008 Dec 31; 58(20):2229-43. PubMed ID: 19209654
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  • 3. How to approach the patient with muscular symptoms in the general neurological practice?
    De Bleecker JL.
    Acta Neurol Belg; 2005 Mar 31; 105(1):18-22. PubMed ID: 15861991
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  • 6. [When should you consider a muscular disease?].
    Pouget J.
    Rev Prat; 2001 Feb 15; 51(3):251-5. PubMed ID: 11265420
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  • 8. [Articulation disorder as the initial manifestation of facioscapulohumeral muscular dystrophy in childhood].
    Lischka A, Grisold W, Weninger M, Toifl K, Tatzer E.
    Klin Padiatr; 1986 Feb 15; 198(2):119-21. PubMed ID: 3702273
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  • 9. [A family of autosomal dominant facio-limb-girdle muscular dystrophy].
    Takao S, Kira J, Kohtake N, Yoshimura T, Goto I.
    Fukuoka Igaku Zasshi; 1996 Dec 15; 87(12):278-82. PubMed ID: 9011111
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  • 12. A clinical approach to muscle diseases.
    Jackson CE.
    Semin Neurol; 2008 Apr 15; 28(2):228-40. PubMed ID: 18351524
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  • 13. Scapuloperoneal myopathy.
    Todman DH, Cooke RA.
    Clin Exp Neurol; 1984 Apr 15; 20():169-74. PubMed ID: 6568938
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  • 14. The clinical and myopathological features of oculopharyngodistal myopathy in a Chinese family.
    Lu H, Luan X, Yuan Y, Dong M, Sun W, Yan C.
    Neuropathology; 2008 Dec 15; 28(6):599-603. PubMed ID: 18503509
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  • 17. Proximal muscle weakness in a 15-year-old boy.
    Felker MV, Garg BP.
    Semin Pediatr Neurol; 2008 Dec 15; 15(4):186-9; discussion 189. PubMed ID: 19073325
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