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 *

114 related articles for article (PubMed ID: 9170393)

  • 1. Dystrophinopathy, the expanding phenotype. Dystrophin abnormalities in X-linked dilated cardiomyopathy.
    Beggs AH
    Circulation; 1997 May; 95(10):2344-7. PubMed ID: 9170393
    [No Abstract]   [Full Text] [Related]  

  • 2. [X-linked dilated cardiomyopathy: a cardiospecific phenotype of dystrophinopathy].
    Yoshida K; Takeda S
    Ryoikibetsu Shokogun Shirizu; 2001; (35):23-7. PubMed ID: 11555918
    [No Abstract]   [Full Text] [Related]  

  • 3. Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy.
    Muntoni F; Di Lenarda A; Porcu M; Sinagra G; Mateddu A; Marrosu G; Ferlini A; Cau M; Milasin J; Melis MA; Marrosu MG; Cianchetti C; Sanna A; Falaschi A; Camerini F; Giacca M; Mestroni L
    Heart; 1997 Dec; 78(6):608-12. PubMed ID: 9470882
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy.
    Ortiz-Lopez R; Li H; Su J; Goytia V; Towbin JA
    Circulation; 1997 May; 95(10):2434-40. PubMed ID: 9170407
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dilated cardiomyopathy and the dystrophin gene: an illustrated review.
    Oldfors A; Eriksson BO; Kyllerman M; Martinsson T; Wahlström J
    Br Heart J; 1994 Oct; 72(4):344-8. PubMed ID: 7833192
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [The heartache of muscular dystrophy].
    Hoogerwaard EM; Ginjaar HB; Wilde AA; Leschot NJ; de Voogt WG; de Visser M
    Ned Tijdschr Geneeskd; 2000 Nov; 144(46):2181-4. PubMed ID: 11103252
    [TBL] [Abstract][Full Text] [Related]  

  • 7. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.
    Towbin JA; Hejtmancik JF; Brink P; Gelb B; Zhu XM; Chamberlain JS; McCabe ER; Swift M
    Circulation; 1993 Jun; 87(6):1854-65. PubMed ID: 8504498
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathy.
    Feng J; Yan JY; Buzin CH; Sommer SS; Towbin JA
    J Am Coll Cardiol; 2002 Sep; 40(6):1120-4. PubMed ID: 12354438
    [TBL] [Abstract][Full Text] [Related]  

  • 9. X-linked dilated cardiomyopathy and the dystrophin gene.
    Ferlini A; Sewry C; Melis MA; Mateddu A; Muntoni F
    Neuromuscul Disord; 1999 Jul; 9(5):339-46. PubMed ID: 10407857
    [TBL] [Abstract][Full Text] [Related]  

  • 10. X-linked dilated cardiomyopathy with a large hot-spot deletion in the dystrophin gene.
    Tasaki N; Yoshida K; Haruta SI; Kouno H; Ichinose H; Fujimoto Y; Urasawa N; Kawakami T; Taniguchi M; Kurushima S; Shimakura T
    Intern Med; 2001 Dec; 40(12):1215-21. PubMed ID: 11813847
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathy.
    Franz WM; Müller M; Müller OJ; Herrmann R; Rothmann T; Cremer M; Cohn RD; Voit T; Katus HA
    Lancet; 2000 May; 355(9217):1781-5. PubMed ID: 10832829
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dystrophin muscle enhancer 1 is implicated in the activation of non-muscle isoforms in the skeletal muscle of patients with X-linked dilated cardiomyopathy.
    Bastianutto C; Bestard JA; Lahnakoski K; Broere D; De Visser M; Zaccolo M; Pozzan T; Ferlini A; Muntoni F; Patarnello T; Klamut HJ
    Hum Mol Genet; 2001 Nov; 10(23):2627-35. PubMed ID: 11726549
    [TBL] [Abstract][Full Text] [Related]  

  • 13. X-linked dilated cardiomyopathy. Novel mutation of the dystrophin gene.
    Franz WM; Cremer M; Herrmann R; Grünig E; Fogel W; Scheffold T; Goebel HH; Kircheisen R; Kübler W; Voit T
    Ann N Y Acad Sci; 1995 Mar; 752():470-91. PubMed ID: 7755293
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel Rod Domain Duplication in Dystrophin Resulting in X-Linked Dilated Cardiomyopathy.
    Chamberlain RC; Smith EC; Campbell MJ
    Pediatr Neurol; 2015 Nov; 53(5):439-41. PubMed ID: 26294044
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Mutations of the dystrophin gene in dilated cardiomyopathy].
    Shiga N; Akita H; Yokoyama M
    Nihon Rinsho; 2000 Jan; 58(1):123-7. PubMed ID: 10885299
    [TBL] [Abstract][Full Text] [Related]  

  • 16. X-linked dilated cardiomyopathy.
    Bies RD
    N Engl J Med; 1994 Feb; 330(5):368-9; author reply 370. PubMed ID: 8277968
    [No Abstract]   [Full Text] [Related]  

  • 17. A point mutation in the 5' splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy.
    Milasin J; Muntoni F; Severini GM; Bartoloni L; Vatta M; Krajinovic M; Mateddu A; Angelini C; Camerini F; Falaschi A; Mestroni L; Giacca M
    Hum Mol Genet; 1996 Jan; 5(1):73-9. PubMed ID: 8789442
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.
    Muntoni F; Cau M; Ganau A; Congiu R; Arvedi G; Mateddu A; Marrosu MG; Cianchetti C; Realdi G; Cao A
    N Engl J Med; 1993 Sep; 329(13):921-5. PubMed ID: 8361506
    [No Abstract]   [Full Text] [Related]  

  • 19. Molecular basis of hypertrophic and dilated cardiomyopathy.
    Marian AJ; Roberts R
    Tex Heart Inst J; 1994; 21(1):6-15. PubMed ID: 8180512
    [TBL] [Abstract][Full Text] [Related]  

  • 20. X-linked dilated cardiomyopathy.
    Towbin JA; Ortiz-Lopez R
    N Engl J Med; 1994 Feb; 330(5):369-70. PubMed ID: 8123157
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.