These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 4. Adult-onset autosomal dominant limb-girdle muscular dystrophy.
    Chutkow JG, Heffner RR, Kramer AA, Edwards JA.
    Ann Neurol; 1986 Aug; 20(2):240-8. PubMed ID: 3752967
    [Abstract] [Full Text] [Related]

  • 5. 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; 28(5):634-9. PubMed ID: 2260849
    [Abstract] [Full Text] [Related]

  • 6. [Myotubular or centronuclear myopathy; report of a case and review of the literature].
    Pereira de Sousa R, Miranda D, Perpetuo FO, Campos GB, Vuletin JC.
    Arq Neuropsiquiatr; 1977 Sep; 35(3):247-59. PubMed ID: 901263
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 8. Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family.
    Sobrido MJ, Fernández JM, Fontoira E, Pérez-Sousa C, Cabello A, Castro M, Teijeira S, Alvarez S, Mederer S, Rivas E, Seijo-Martínez M, Navarro C.
    Brain; 2005 Jul; 128(Pt 7):1716-27. PubMed ID: 15857933
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 11. [2 families with benign myopathy predominantly on the limb girdle with dominant autosomal heredity].
    Serratrice G, Pellissier JF.
    Rev Neurol (Paris); 1988 Dec; 144(1):43-6. PubMed ID: 3347807
    [Abstract] [Full Text] [Related]

  • 12. Distal muscular dystrophy. Case reports.
    Ishpekova B, Milanov I.
    Electromyogr Clin Neurophysiol; 1997 Dec; 37(4):201-5. PubMed ID: 9208214
    [Abstract] [Full Text] [Related]

  • 13. Distal muscular dystrophy with autosomal recessive inheritance.
    Scoppetta C, Vaccario ML, Casali C, Di Trapani G, Mennuni G.
    Muscle Nerve; 1984 Dec; 7(6):478-81. PubMed ID: 6543900
    [Abstract] [Full Text] [Related]

  • 14. [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; 87(12):278-82. PubMed ID: 9011111
    [Abstract] [Full Text] [Related]

  • 15. Scapuloperoneal myopathy.
    Todman DH, Cooke RA.
    Clin Exp Neurol; 1984 Dec; 20():169-74. PubMed ID: 6568938
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 20. A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement.
    van der Kooi AJ, Ledderhof TM, de Voogt WG, Res CJ, Bouwsma G, Troost D, Busch HF, Becker AE, de Visser M.
    Ann Neurol; 1996 May; 39(5):636-42. PubMed ID: 8619549
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.