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Journal Abstract Search

89 related items for PubMed ID: 1295057

  • 1. [Autosomal dominant centronuclear myopathy].
    Ferrer X, Vital C, Coquet M, Deleplanque B, Ellie E, Lagueny A, Julien J.
    Rev Neurol (Paris); 1992; 148(10):622-30. PubMed ID: 1295057
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  • 2. [A pedigree of autosomal dominant limb-girdle myopathy with rimmed vacuole formation].
    Kishibayashi J, Sunohara N, Saito Y.
    Rinsho Shinkeigaku; 1997 Jul; 37(7):603-10. PubMed ID: 9396357
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  • 3. [Familial form of centronuclear myopathy in the adult].
    Pépin B, Mikol J, Goldstein B, Haguenau M, Godlewski S.
    Rev Neurol (Paris); 1976 Dec; 132(12):845-57. PubMed ID: 1013570
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  • 7. [Early-onset benign autosomal dominant limb-girdle myopathy with contractures (Bethlem myopathy) in a Japanese family].
    Sasabe F, Takase Y, Fukusako T, Yamamoto K, Morimatsu M.
    Rinsho Shinkeigaku; 1992 Feb; 32(2):138-42. PubMed ID: 1611771
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  • 9. A novel autosomal dominant distal myopathy with early respiratory failure: clinico-pathologic characteristics and exclusion of linkage to candidate genetic loci.
    Chinnery PF, Johnson MA, Walls TJ, Gibson GJ, Fawcett PR, Jamieson S, Fulthorpe JJ, Cullen M, Hudgson P, Bushby KM.
    Ann Neurol; 2001 Apr; 49(4):443-52. PubMed ID: 11310621
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  • 10. Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients.
    Kley RA, Hellenbroich Y, van der Ven PF, Fürst DO, Huebner A, Bruchertseifer V, Peters SA, Heyer CM, Kirschner J, Schröder R, Fischer D, Müller K, Tolksdorf K, Eger K, Germing A, Brodherr T, Reum C, Walter MC, Lochmüller H, Ketelsen UP, Vorgerd M.
    Brain; 2007 Dec; 130(Pt 12):3250-64. PubMed ID: 18055494
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  • 12. Distal muscular dystrophy. Case reports.
    Ishpekova B, Milanov I.
    Electromyogr Clin Neurophysiol; 1997 Dec; 37(4):201-5. PubMed ID: 9208214
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  • 16. [A rare case of adult-onset Becker muscular dystrophy diagnosed by dystrophin staining].
    Ujike H, Tomita J, Kuroda S, Otsuki S, Arahata K.
    No To Shinkei; 1991 Oct; 43(10):975-9. PubMed ID: 1724729
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  • 17. Centronuclear myopathy: follow-up study of a case reported as an early onset myopathy (1966): muscle biopsies in parents and sibs.
    Mercelis R, Martin JJ, Martin L, Ceuterick C.
    Acta Neurol Belg; 1980 Oct; 80(6):348-60. PubMed ID: 7468147
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  • 18. [Autosomal recessive severe, proximal myopathy in children, common in Tunisia].
    Ben Hamida M, Attia N, Chabouni H, Fardeau M.
    Rev Neurol (Paris); 1983 Oct; 139(4):289-97. PubMed ID: 6612142
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  • 19. Distal muscular dystrophy of the Miyoshi type.
    Yildiz H, Emre U, Coskun O, Ergün U, Atasoy HT, Inan LE.
    Clin Neuropathol; 2003 Oct; 22(4):204-8. PubMed ID: 12908758
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