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Journal Abstract Search

278 related items for PubMed ID: 8619549

  • 21.
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  • 22. [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
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  • 23. Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy.
    van der Kooi AJ, Bonne G, Eymard B, Duboc D, Talim B, Van der Valk M, Reiss P, Richard P, Demay L, Merlini L, Schwartz K, Busch HF, de Visser M.
    Neurology; 2002 Aug 27; 59(4):620-3. PubMed ID: 12196663
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  • 24.
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  • 25. Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease.
    Jakobs PM, Hanson EL, Crispell KA, Toy W, Keegan H, Schilling K, Icenogle TB, Litt M, Hershberger RE.
    J Card Fail; 2001 Sep 27; 7(3):249-56. PubMed ID: 11561226
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  • 26.
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  • 27. Limb-girdle muscular dystrophy due to emerin gene mutations.
    Ura S, Hayashi YK, Goto K, Astejada MN, Murakami T, Nagato M, Ohta S, Daimon Y, Takekawa H, Hirata K, Nonaka I, Noguchi S, Nishino I.
    Arch Neurol; 2007 Jul 27; 64(7):1038-41. PubMed ID: 17620497
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  • 28.
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  • 29. [Cardiac dysfunction in female gene carriers of Duchenne muscular dystrophy].
    Ueda Y, Kawai H, Adachi K, Naruo T, Saito S.
    Rinsho Shinkeigaku; 1995 Nov 27; 35(11):1191-8. PubMed ID: 8720327
    [Abstract] [Full Text] [Related]

  • 30. A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12.
    Jarry J, Rioux MF, Bolduc V, Robitaille Y, Khoury V, Thiffault I, Tétreault M, Loisel L, Bouchard JP, Brais B.
    Brain; 2007 Feb 27; 130(Pt 2):368-80. PubMed ID: 17008331
    [Abstract] [Full Text] [Related]

  • 31.
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  • 32. Limb girdle muscular dystrophy: description of a phenotype.
    Stübgen JP.
    Muscle Nerve; 1994 Dec 27; 17(12):1449-55. PubMed ID: 7969245
    [Abstract] [Full Text] [Related]

  • 33. 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 Dec 27; 2(4):232-41. PubMed ID: 11252708
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  • 34.
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  • 35. The limb-girdle muscular dystrophies: diagnostic guidelines.
    Bushby KM.
    Eur J Paediatr Neurol; 1999 Dec 27; 3(2):53-8. PubMed ID: 10700539
    [Abstract] [Full Text] [Related]

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  • 37.
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  • 38. Cardiac involvement in patients with limb-girdle muscular dystrophy type 2 and Becker muscular dystrophy.
    Sveen ML, Thune JJ, Køber L, Vissing J.
    Arch Neurol; 2008 Sep 27; 65(9):1196-201. PubMed ID: 18779423
    [Abstract] [Full Text] [Related]

  • 39. 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 27; 130(Pt 12):3250-64. PubMed ID: 18055494
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  • 40.
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