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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 9052806)

  • 1. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Danish family with limb-girdle muscular dystrophy with autosomal dominant inheritance.
    Nielsen JF; Jakobsen J
    Neuromuscul Disord; 1994 Mar; 4(2):139-42. PubMed ID: 8012194
    [TBL] [Abstract][Full Text] [Related]  

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

  • 13. Late onset foot-drop muscular dystrophy with rimmed vacuoles.
    Partanen J; Laulumaa V; Paljärvi L; Partanen K; Naukkarinen A
    J Neurol Sci; 1994 Sep; 125(2):158-67. PubMed ID: 7807161
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Emery-Dreifuss muscular dystrophy and other related disorders.
    Emery AE
    Br Med Bull; 1989 Jul; 45(3):772-87. PubMed ID: 2688828
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Muscular dystrophy with separate clinical phenotypes in a large family.
    Udd B; Kääriänen H; Somer H
    Muscle Nerve; 1991 Nov; 14(11):1050-8. PubMed ID: 1745277
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 7(3):249-56. PubMed ID: 11561226
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Abnormal merosin in adults. A new form of late onset muscular dystrophy not linked to chromosome 6q2.
    Bushby K; Anderson LV; Pollitt C; Naom I; Muntoni F; Bindoff L
    Brain; 1998 Apr; 121 ( Pt 4)():581-8. PubMed ID: 9577386
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 108(3):187-91. PubMed ID: 11891683
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Merosin-positive congenital muscular dystrophy: a large inbred family.
    Mahjneh I; Bushby K; Anderson L; Muntoni F; Tolvanen-Mahjneh H; Bashir R; Pizzi A; Brockington M; Marconi G
    Neuropediatrics; 1999 Feb; 30(1):22-8. PubMed ID: 10222457
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Late-onset autosomal dominant limb girdle muscular dystrophy and Paget's disease of bone unlinked to the VCP gene locus.
    Kottlors M; Moske-Eick O; Huebner A; Krause S; Mueller K; Kress W; Schwarzwald R; Bornemann A; Haug V; Heitzer M; Kirschner J
    J Neurol Sci; 2010 Apr; 291(1-2):79-85. PubMed ID: 20116073
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.