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

106 related items for PubMed ID: 3347807

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

  • 2. 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]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 5. [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]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. [Calpain-3 gene defect causing limb gird muscular dystrophy in a Hungarian family].
    Horváth R, Walter MC, Lochmüller H, Hübner A, Karcagi V, Pikó H, Timár L, Komoly S.
    Ideggyogy Sz; 2005 Jan 20; 58(1-2):52-8. PubMed ID: 15884399
    [Abstract] [Full Text] [Related]

  • 8. [Clinical and genetic heterogeneity of limb-girdle muscular dystrophy].
    Kozłowska M.
    Neurol Neurochir Pol; 1995 Jan 20; 29(4):569-75. PubMed ID: 8544936
    [Abstract] [Full Text] [Related]

  • 9. [Emery-Dreifuss disease or syndrome of amyotrophy with early contractures and secondary disorders of cardiac conduction with variable heredity].
    Serratrice G, Pouget J.
    Rev Neurol (Paris); 1986 Jan 20; 142(10):766-70. PubMed ID: 3823708
    [Abstract] [Full Text] [Related]

  • 10. [Autosomal dominant centronuclear myopathy].
    Ferrer X, Vital C, Coquet M, Deleplanque B, Ellie E, Lagueny A, Julien J.
    Rev Neurol (Paris); 1992 Jan 20; 148(10):622-30. PubMed ID: 1295057
    [Abstract] [Full Text] [Related]

  • 11. [Autosomal recessive severe, proximal myopathy in children, common in Tunisia].
    Ben Hamida M, Attia N, Chabouni H, Fardeau M.
    Rev Neurol (Paris); 1983 Jan 20; 139(4):289-97. PubMed ID: 6612142
    [Abstract] [Full Text] [Related]

  • 12. [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 20; 41(10):586-95. PubMed ID: 2608758
    [Abstract] [Full Text] [Related]

  • 13. A Danish family with limb-girdle muscular dystrophy with autosomal dominant inheritance.
    Nielsen JF, Jakobsen J.
    Neuromuscul Disord; 1994 Mar 20; 4(2):139-42. PubMed ID: 8012194
    [Abstract] [Full Text] [Related]

  • 14. 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 20; 39(5):636-42. PubMed ID: 8619549
    [Abstract] [Full Text] [Related]

  • 15. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
    Bonne G, Mercuri E, Muchir A, Urtizberea A, Bécane HM, Recan D, Merlini L, Wehnert M, Boor R, Reuner U, Vorgerd M, Wicklein EM, Eymard B, Duboc D, Penisson-Besnier I, Cuisset JM, Ferrer X, Desguerre I, Lacombe D, Bushby K, Pollitt C, Toniolo D, Fardeau M, Schwartz K, Muntoni F.
    Ann Neurol; 2000 Aug 20; 48(2):170-80. PubMed ID: 10939567
    [Abstract] [Full Text] [Related]

  • 16. 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 20; 128(Pt 7):1716-27. PubMed ID: 15857933
    [Abstract] [Full Text] [Related]

  • 17. Distal muscular dystrophy with autosomal recessive inheritance.
    Scoppetta C, Vaccario ML, Casali C, Di Trapani G, Mennuni G.
    Muscle Nerve; 1984 Jul 20; 7(6):478-81. PubMed ID: 6543900
    [Abstract] [Full Text] [Related]

  • 18. [Scapular-peroneal amyotrophy as one of the forms of progressive muscular dystrophy].
    Dracheva ZN, Iablokova MS, Lutvinenko NI.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1970 Jul 20; 70(3):337-41. PubMed ID: 5419678
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Two novel CAV3 gene mutations in Japanese families.
    Sugie K, Murayama K, Noguchi S, Murakami N, Mochizuki M, Hayashi YK, Nonaka I, Nishino I.
    Neuromuscul Disord; 2004 Dec 20; 14(12):810-4. PubMed ID: 15564037
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.