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Journal Abstract Search

208 related items for PubMed ID: 286404

  • 1. Quadriceps myopathy in two brothers: rare familial myopathy confirmed by muscle biopsy.
    Finelli PF.
    R I Med J (1976); 1979 Apr; 62(4):125-9. PubMed ID: 286404
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  • 2. [Quadriceps myopathy or amyotrophic quadriceps syndrome. Nosologic study apropos of 10 cases].
    Serratrice G, Gastaut JL, Pellissier JF, Cros D, Pouget J.
    Rev Neurol (Paris); 1983 Apr; 139(5):367-73. PubMed ID: 6612146
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  • 5. Chronic neurogenic quadriceps amyotrophy.
    Furukawa T, Akagami N, Maruyama S.
    Ann Neurol; 1977 Dec; 2(6):528-30. PubMed ID: 617595
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  • 6. Nemaline myopathy and a mitochondrial neuromuscular disorder in one family.
    Shapira YA, Yarom R, Blank A.
    Neuropediatrics; 1981 May; 12(2):152-65. PubMed ID: 6267500
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  • 7. Type I muscle fibre atrophy and central nuclei. A rare familial neuromuscular disease.
    Karpati G, Carpenter S, Nelson RF.
    J Neurol Sci; 1970 May; 10(5):489-500. PubMed ID: 4910660
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  • 9. [Unknown cause of familial neuromuscular disease with infiltration of cytotoxic/suppressor T cells].
    Fukunaga H, Kitajima I, Sonoda Y, Atuchi H.
    Rinsho Shinkeigaku; 1990 Jun; 30(6):654-8. PubMed ID: 2146056
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  • 10. [Facioscapulohumeral neuromuscular syndromes--problems of differential and early diagnosis and genetic counseling].
    Bachmann H, Ziegan J, Steinbicker V, von Rohden L, Wagner A.
    Psychiatr Neurol Med Psychol (Leipz); 1989 Oct; 41(10):586-95. PubMed ID: 2608758
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  • 13. Familial nemaline myopathy.
    Scarlato G, Pellegrini G, Moggio M, Meola G, Cordone G, Minetti C, Lester A.
    Neuropediatrics; 1982 Nov; 13(4):211-5. PubMed ID: 6296713
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  • 14. [Role of MRI in the diagnosis of neuromuscular disorders].
    Pál E, Dérczy K.
    Orv Hetil; 2011 Aug 21; 152(34):1362-7. PubMed ID: 21835742
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  • 15. Quadriceps myopathy: forme fruste of Becker muscular dystrophy.
    Sunohara N, Arahata K, Hoffman EP, Yamada H, Nishimiya J, Arikawa E, Kaido M, Nonaka I, Sugita H.
    Ann Neurol; 1990 Nov 21; 28(5):634-9. PubMed ID: 2260849
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  • 16. MRI in myopathy.
    Lovitt S, Marden FA, Gundogdu B, Ostrowski ML.
    Neurol Clin; 2004 Aug 21; 22(3):509-38, v. PubMed ID: 15207874
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  • 20. Myopathy in a patient with chromosome 22q11 deletion.
    Mongini T, Doriguzzi C, Arduino C, Brusco A, Bortolotto S, Mutani R, Palmucci L.
    Neuropediatrics; 2001 Apr 21; 32(2):107-9. PubMed ID: 11414642
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