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Journal Abstract Search

278 related items for PubMed ID: 8619549

  • 1. 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; 39(5):636-42. PubMed ID: 8619549
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  • 4. [A pedigree of autosomal dominant limb-girdle myopathy with rimmed vacuole formation].
    Kishibayashi J, Sunohara N, Saito Y.
    Rinsho Shinkeigaku; 1997 Jul; 37(7):603-10. PubMed ID: 9396357
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  • 5. [The first Japanese case of autosomal dominant Emery-Dreifuss muscular dystrophy with a novel mutation in the lamin A/C gene].
    Onishi Y, Higuchi J, Ogawa T, Namekawa A, Hayashi H, Odakura H, Goto K, Hayashi YK.
    Rinsho Shinkeigaku; 2002 Feb; 42(2):140-4. PubMed ID: 12424964
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  • 7. 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; 79(1):73-7. PubMed ID: 9505924
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  • 9. Childhood-onset autosomal-dominant limb-girdle muscular dystrophy with cardiac conduction block.
    Fang W, Huang CC, Chu NS, Chen CJ, Lu CS, Wang CC.
    Muscle Nerve; 1997 Mar; 20(3):286-92. PubMed ID: 9052806
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  • 10. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21.
    Starling A, Kok F, Passos-Bueno MR, Vainzof M, Zatz M.
    Eur J Hum Genet; 2004 Dec; 12(12):1033-40. PubMed ID: 15367920
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  • 11. [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
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  • 13. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics.
    van Tintelen JP, Hofstra RM, Katerberg H, Rossenbacker T, Wiesfeld AC, du Marchie Sarvaas GJ, Wilde AA, van Langen IM, Nannenberg EA, van der Kooi AJ, Kraak M, van Gelder IC, van Veldhuisen DJ, Vos Y, van den Berg MP, Working Group on Inherited Cardiac Disorders, line 27/50, Interuniversity Cardiology Institute of The Netherlands.
    Am Heart J; 2007 Dec; 154(6):1130-9. PubMed ID: 18035086
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  • 15. High incidence of sudden cardiac death with conduction disturbances and atrial cardiomyopathy caused by a nonsense mutation in the STA gene.
    Sakata K, Shimizu M, Ino H, Yamaguchi M, Terai H, Fujino N, Hayashi K, Kaneda T, Inoue M, Oda Y, Fujita T, Kaku B, Kanaya H, Mabuchi H.
    Circulation; 2005 Jun 28; 111(25):3352-8. PubMed ID: 15967842
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  • 16. Adult onset limb-girdle muscular dystrophy with autosomal dominant inheritance.
    Somer H, Laulumaa V, Paljärvi L, Partanen J, Haltia M.
    Prog Clin Biol Res; 1989 Jun 28; 306():69-71. PubMed ID: 2740412
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  • 17. [Hauptmann-Thannhauser muscular dystrophy and differential diagnosis of myopathies associated with contractures].
    Hanisch F, Neudecker S, Wehnert M, Zierz S.
    Nervenarzt; 2002 Oct 28; 73(10):1004-11. PubMed ID: 12376891
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  • 18. [Clinical and genetic heterogeneity of limb-girdle muscular dystrophy].
    Kozłowska M.
    Neurol Neurochir Pol; 1995 Oct 28; 29(4):569-75. PubMed ID: 8544936
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