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

310 related items for PubMed ID: 8741343

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries.
    Fardeau M, Matsumura K, Tomé FM, Collin H, Leturcq F, Kaplan JC, Campbell KP.
    C R Acad Sci III; 1993 Aug; 316(8):799-804. PubMed ID: 8044705
    [Abstract] [Full Text] [Related]

  • 23. Novel mutations in three patients with LGMD2C with phenotypic differences.
    Vermeer S, Verrips A, Willemsen MA, ter Laak HJ, Ginjaar IB, Hamel BC.
    Pediatr Neurol; 2004 Apr; 30(4):291-4. PubMed ID: 15087111
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the gamma-sarcoglycan gene.
    Lasa A, Piccolo F, de Diego C, Jeanpierre M, Colomer J, Rodríguez MJ, Urtizberea JA, Baiget M, Kaplan J, Gallano P.
    Eur J Hum Genet; 1998 Apr; 6(4):396-9. PubMed ID: 9781048
    [Abstract] [Full Text] [Related]

  • 26. [Muscular dystrophy due to a mutation in the gene of alpha-sarcoglycan subunit of dystrophin associated protein complex].
    Urtasun M, Poza JJ, Gallano P, Lasa A, Sáenz A, Cobo AM, Leturcq F, López de Munain A, García-Bragado F.
    Med Clin (Barc); 1998 Apr 25; 110(14):538-42. PubMed ID: 9646269
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2).
    Duggan DJ, Manchester D, Stears KP, Mathews DJ, Hart C, Hoffman EP.
    Neurogenetics; 1997 May 25; 1(1):49-58. PubMed ID: 10735275
    [Abstract] [Full Text] [Related]

  • 33. New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiency.
    Higuchi I, Iwaki H, Kawai H, Endo T, Kunishige M, Fukunaga H, Nakagawa M, Arimura K, Osame M.
    J Neurol Sci; 1997 Dec 09; 153(1):100-5. PubMed ID: 9455986
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. [Dystrophinopathies, congenital muscular dystrophy, limb-girdle dystrophies: updated classification].
    Teijeira-Bautista S, García-García D, Teijeiro-Ferreira A, Fernández-Hojas R, Fernández-Rodríguez JM, Navarro-Fernández-Balbuena C.
    Rev Neurol; 1998 Jun 09; 26(154):1021-6. PubMed ID: 9658487
    [Abstract] [Full Text] [Related]

  • 36. Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy.
    Fadic R, Sunada Y, Waclawik AJ, Buck S, Lewandoski PJ, Campbell KP, Lotz BP.
    N Engl J Med; 1996 Feb 08; 334(6):362-6. PubMed ID: 8538707
    [No Abstract] [Full Text] [Related]

  • 37. The childhood muscular dystrophies: making order out of chaos.
    Tsao CY, Mendell JR.
    Semin Neurol; 1999 Feb 08; 19(1):9-23. PubMed ID: 10711985
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Ultrastructural localization of adhalin, alpha-dystroglycan and merosin in normal and dystrophic muscle.
    Cullen MJ, Walsh J, Roberds SL, Campbell KP.
    Neuropathol Appl Neurobiol; 1996 Feb 08; 22(1):30-7. PubMed ID: 8866780
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 16.