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

278 related items for PubMed ID: 8619549

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
    Bonne G, Mercuri E, Muchir A, Urtizberea A, Bécane HM, Recan D, Merlini L, Wehnert M, Boor R, Reuner U, Vorgerd M, Wicklein EM, Eymard B, Duboc D, Penisson-Besnier I, Cuisset JM, Ferrer X, Desguerre I, Lacombe D, Bushby K, Pollitt C, Toniolo D, Fardeau M, Schwartz K, Muntoni F.
    Ann Neurol; 2000 Aug; 48(2):170-80. PubMed ID: 10939567
    [Abstract] [Full Text] [Related]

  • 3. Cardiac dysrhythmias,cardiomyopathy and muscular dystrophy in patients with Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy type 1B.
    Hong JS, Ki CS, Kim JW, Suh YL, Kim JS, Baek KK, Kim BJ, Ahn KJ, Kim DK.
    J Korean Med Sci; 2005 Apr; 20(2):283-90. PubMed ID: 15832002
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

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

  • 6. Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles.
    Nakamura A, Yoshida K, Ikeda S.
    Clin Neurol Neurosurg; 2004 Mar; 106(2):122-8. PubMed ID: 15003303
    [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. 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
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Emery-dreifuss humeroperoneal muscular dystrophy: an x-linked myopathy with unusual contractures and bradycardia.
    Hopkins LC, Jackson JA, Elsas LJ.
    Ann Neurol; 1981 Sep; 10(3):230-7. PubMed ID: 7294729
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 14. Adult-onset autosomal dominant limb-girdle muscular dystrophy.
    Chutkow JG, Heffner RR, Kramer AA, Edwards JA.
    Ann Neurol; 1986 Aug; 20(2):240-8. PubMed ID: 3752967
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 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 Aug; 306():69-71. PubMed ID: 2740412
    [No Abstract] [Full Text] [Related]

  • 17. [Hauptmann-Thannhauser muscular dystrophy and differential diagnosis of myopathies associated with contractures].
    Hanisch F, Neudecker S, Wehnert M, Zierz S.
    Nervenarzt; 2002 Oct; 73(10):1004-11. PubMed ID: 12376891
    [Abstract] [Full Text] [Related]

  • 18. [Clinical and genetic heterogeneity of limb-girdle muscular dystrophy].
    Kozłowska M.
    Neurol Neurochir Pol; 1995 Oct; 29(4):569-75. PubMed ID: 8544936
    [Abstract] [Full Text] [Related]

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

  • 20. Malignant mutation in the lamin A/C gene causing progressive conduction system disease and early sudden death in a family with mild form of limb-girdle muscular dystrophy.
    Antoniades L, Eftychiou C, Kyriakides T, Christodoulou K, Katritsis DG.
    J Interv Card Electrophysiol; 2007 Jun; 19(1):1-7. PubMed ID: 17605093
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.