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 *

123 related articles for article (PubMed ID: 3953067)

  • 1. Familial automaticity-conduction disorder with associated cardiomyopathy.
    Greenlee PR; Anderson JL; Lutz JR; Lindsay AE; Hagan AD
    West J Med; 1986 Jan; 144(1):33-41. PubMed ID: 3953067
    [TBL] [Abstract][Full Text] [Related]  

  • 2. New phenotype of familial dilated cardiomyopathy and conduction disorders.
    Oropeza ES; Cadena CN
    Am Heart J; 2003 Feb; 145(2):317-23. PubMed ID: 12595850
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation.
    Hershberger RE; Hanson EL; Jakobs PM; Keegan H; Coates K; Bousman S; Litt M
    Am Heart J; 2002 Dec; 144(6):1081-6. PubMed ID: 12486434
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial dilated cardiomyopathy: evidence for clinical and immunogenetic heterogeneity.
    Bilińska ZT; Michalak E; Piatosa B; Grzybowski J; Skwarek M; Deptuch TW; Kuśmierczyk-Droszcz B; Piotrowski W; Ruzyłło W
    Med Sci Monit; 2003 May; 9(5):CR167-74. PubMed ID: 12761452
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Familial dilated cardiomyopathy with autosomal mode of inheritance. Case report].
    Dzielińska Z; Michalak E; Bilińska ZT; Walczak E; Demkow M; Chojnowska L; Ruzyłło W; Rydlewska-Sadowska W; Popławska W; Lewicki Z
    Kardiol Pol; 1993 Dec; 39(12):473-7. PubMed ID: 8289434
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1.
    Kass S; MacRae C; Graber HL; Sparks EA; McNamara D; Boudoulas H; Basson CT; Baker PB; Cody RJ; Fishman MC
    Nat Genet; 1994 Aug; 7(4):546-51. PubMed ID: 7951328
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.
    Bowles KR; Gajarski R; Porter P; Goytia V; Bachinski L; Roberts R; Pignatelli R; Towbin JA
    J Clin Invest; 1996 Sep; 98(6):1355-60. PubMed ID: 8823300
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial idiopathic congestive cardiomyopathy in three generations: a family study with eight affected members.
    MacLennan BA; Tsoi EY; Maguire C; Adgey AA
    Q J Med; 1987 Apr; 63(240):335-47. PubMed ID: 3685246
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Genetic linkage analysis in localizing a gene of autosomal dominant familial dilated cardiomyopathy with conduction defect].
    Xu W; Zhang BR; Hu ZM; Pan Q; Liu XP; Liang DS; Wu LQ; Cai F; Long ZG; Xia K; Xia JH
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2005 Oct; 30(5):510-4. PubMed ID: 16320577
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial dilated cardiomyopathy.
    Schmidt MA; Michels VV; Edwards WD; Miller FA
    Am J Med Genet; 1988 Sep; 31(1):135-43. PubMed ID: 3223495
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Rhythm and conduction disorders in familial myocardiopathy].
    Hurtado Buen Abad L; Elizalde Galván A; Cárdenas M
    Arch Inst Cardiol Mex; 1976; 46(3):253-61. PubMed ID: 802962
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 111(25):3352-8. PubMed ID: 15967842
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial atrial tachyarrhythmia with short PR interval.
    Brodsky M; Wu D; Denes P; Rosen KM
    Arch Intern Med; 1977 Feb; 137(2):165-9. PubMed ID: 836114
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial progressive sinoatrial and atrioventricular conduction disease of adult onset with sudden death, dilated cardiomyopathy, and brachydactyly. A new type of heart-hand syndrome?
    Sinkovec M; Petrovic D; Volk M; Peterlin B
    Clin Genet; 2005 Aug; 68(2):155-60. PubMed ID: 15996213
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dominantly inherited dilated cardiomyopathy.
    Gardner RJ; Hanson JW; Ionasescu VV; Ardinger HH; Skorton DJ; Mahoney LT; Hart MN; Rose EF; Smith WL; Florentine MS
    Am J Med Genet; 1987 May; 27(1):61-73. PubMed ID: 3605207
    [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. 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]  

  • 18. Evidence-based diagnosis of familial non-X-linked dilated cardiomyopathy. Prevalence, inheritance and characteristics.
    Gavazzi A; Repetto A; Scelsi L; Inserra C; Laudisa ML; Campana C; Specchia C; Dal Bello B; Diegoli M; Tavazzi L; Arbustini E
    Eur Heart J; 2001 Jan; 22(1):73-81. PubMed ID: 11133212
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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;
    Am Heart J; 2007 Dec; 154(6):1130-9. PubMed ID: 18035086
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Functional consequences of an LMNA mutation associated with a new cardiac and non-cardiac phenotype.
    Charniot JC; Pascal C; Bouchier C; Sébillon P; Salama J; Duboscq-Bidot L; Peuchmaurd M; Desnos M; Artigou JY; Komajda M
    Hum Mutat; 2003 May; 21(5):473-81. PubMed ID: 12673789
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.