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

Journal Abstract Search


128 related items for PubMed ID: 10478586

  • 1. Autosomal dominant limb-girdle muscular dystrophy with ankle joint contracture.
    Tanaka K, Yamada T, Kikuchi H, Mitsunaga Y, Furuya H, Kira J.
    Acta Neurol Scand; 1999 Sep; 100(3):199-201. PubMed ID: 10478586
    [Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone.
    Kimonis VE, Kovach MJ, Waggoner B, Leal S, Salam A, Rimer L, Davis K, Khardori R, Gelber D.
    Genet Med; 2000 Feb; 2(4):232-41. PubMed ID: 11252708
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. A missense mutation in the exon 8 of lamin A/C gene in a Japanese case of autosomal dominant limb-girdle muscular dystrophy and cardiac conduction block.
    Kitaguchi T, Matsubara S, Sato M, Miyamoto K, Hirai S, Schwartz K, Bonne G.
    Neuromuscul Disord; 2001 Sep; 11(6-7):542-6. PubMed ID: 11525883
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophy.
    Gilchrist JM, Pericak-Vance M, Silverman L, Roses AD.
    Neurology; 1988 Jan; 38(1):5-9. PubMed ID: 3275904
    [Abstract] [Full Text] [Related]

  • 11. Heterogeneity in familial dominant Paget disease of bone and muscular dystrophy.
    Waggoner B, Kovach MJ, Winkelman M, Cai D, Khardori R, Gelber D, Kimonis VE.
    Am J Med Genet; 2002 Mar 15; 108(3):187-91. PubMed ID: 11891683
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No 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 15; 4(2):139-42. PubMed ID: 8012194
    [Abstract] [Full Text] [Related]

  • 14. [Proximal muscular dystrophy with contractures and malignant course: is it a variant of Emery-Dreifuss disease?].
    Badalian Lo, Temin PA, Kalinin VA, Arkhipov BA, Zabadenko NN, Voloshina TG, Lysov VL.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1990 Mar 15; 90(3):52-6. PubMed ID: 2163170
    [Abstract] [Full Text] [Related]

  • 15. Limb girdle muscular dystrophy with autosomal dominant inheritance.
    Marconi G, Pizzi A, Arimondi CG, Vannelli B.
    Acta Neurol Scand; 1991 Apr 15; 83(4):234-8. PubMed ID: 2048397
    [Abstract] [Full Text] [Related]

  • 16. The heart in limb girdle muscular dystrophy.
    van der Kooi AJ, de Voogt WG, Barth PG, Busch HF, Jennekens FG, Jongen PJ, de Visser M.
    Heart; 1998 Jan 15; 79(1):73-7. PubMed ID: 9505924
    [Abstract] [Full Text] [Related]

  • 17. [A pedigree of autosomal dominant limb-girdle myopathy with rimmed vacuole formation].
    Kishibayashi J, Sunohara N, Saito Y.
    Rinsho Shinkeigaku; 1997 Jul 15; 37(7):603-10. PubMed ID: 9396357
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 7.