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

  • 41. [Progressive pseudomyopathic spinal amyotrophies (author's transl)].
    Arnetoli G, Marconi GP, Marini P.
    Riv Patol Nerv Ment; 1976; 96(1):35-53. PubMed ID: 785577
    [Abstract] [Full Text] [Related]

  • 42. Bethlem myopathy in a Taiwanese family.
    Lien LM, Yang CC, Chen WH, Chiu HC.
    J Formos Med Assoc; 2001 Jun; 100(6):416-9. PubMed ID: 11480253
    [Abstract] [Full Text] [Related]

  • 43.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 44. Genetic localization of Bethlem myopathy.
    Jobsis GJ, Bolhuis PA, Boers JM, Baas F, Wolterman RA, Hensels GW, de Visser M.
    Neurology; 1996 Mar; 46(3):779-82. PubMed ID: 8618682
    [Abstract] [Full Text] [Related]

  • 45. Autosomal dominant humeroperoneal myopathy.
    Gilchrist JM, Leshner RT.
    Arch Neurol; 1986 Jul; 43(7):734-5. PubMed ID: 3729752
    [Abstract] [Full Text] [Related]

  • 46. Early-onset benign limb-girdle myopathy with contractures and facial involvement affecting a father and daughter.
    Malandrini A, Scarpini C, Fabrizi GM, Parrotta E, Salvadori C, Guazzi GC.
    J Neurol Sci; 1995 Oct; 132(2):195-200. PubMed ID: 8543948
    [Abstract] [Full Text] [Related]

  • 47. [Distal myopathy].
    Badurska B, Pfeffer-Baczuk A.
    Neurol Neurochir Pol; 1985 Oct; 19(6):512-5. PubMed ID: 3835492
    [Abstract] [Full Text] [Related]

  • 48. Muscular dystrophy in Northern Ireland. III. Linkage data with particular reference to autosomal limb girdle muscular dystrophy.
    STEVENSON AC, CHEESEMAN EA.
    Ann Hum Genet; 1955 Feb; 19(3):165-73. PubMed ID: 14350450
    [No Abstract] [Full Text] [Related]

  • 49. The clinical spectrum of limb girdle muscular dystrophy. A survey in The Netherlands.
    van der Kooi AJ, Barth PG, Busch HF, de Haan R, Ginjaar HB, van Essen AJ, van Hooff LJ, Höweler CJ, Jennekens FG, Jongen P, Oosterhuis HJ, Padberg GW, Spaans F, Wintzen AR, Wokke JH, Bakker E, van Ommen GJ, Bolhuis PA, de Visser M.
    Brain; 1996 Oct; 119 ( Pt 5)():1471-80. PubMed ID: 8931572
    [Abstract] [Full Text] [Related]

  • 50.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 51. Differential diagnosis of limb-girdle muscular dystrophy and spinal muscular atrophy.
    Coërs C, Telerman-Toppet N.
    Neurology; 1979 Jul; 29(7):957-72. PubMed ID: 572945
    [Abstract] [Full Text] [Related]

  • 52.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 53.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 54.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 55.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 56. Living with a hereditary disease: persons with muscular dystrophy and their next of kin.
    Boström K, Ahlström G.
    Am J Med Genet A; 2005 Jul 01; 136(1):17-24. PubMed ID: 15889411
    [Abstract] [Full Text] [Related]

  • 57. Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin beta 1?
    Taylor J, Muntoni F, Robb S, Dubowitz V, Sewry C.
    Neuromuscul Disord; 1997 Jun 01; 7(4):211-6. PubMed ID: 9196901
    [Abstract] [Full Text] [Related]

  • 58. Autosomal recessive inheritance of Duchennetype muscular dystrophy.
    KLOEPFER HW, TALLEY C.
    Ann Hum Genet; 1958 Feb 01; 22(2):138-43. PubMed ID: 13509526
    [No Abstract] [Full Text] [Related]

  • 59.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 60.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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