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 *

80 related articles for article (PubMed ID: 5007810)

  • 1. Familial atrial cardiomyopathy with heart block.
    Nagle RE; Smith B; Williams DO
    Br Heart J; 1972 Feb; 34(2):205. PubMed ID: 5007810
    [No Abstract]   [Full Text] [Related]  

  • 2. [Familial cardiomyopathy in 2 brothers with heart block and auricular flutter].
    Dake F; Nakayama H; Hayashi T
    Naika; 1966 Dec; 18(7):1349-53. PubMed ID: 5980317
    [No Abstract]   [Full Text] [Related]  

  • 3. Familial atrial cardiomyopathy with heart block.
    Williams DO; Jones EL; Nagle RE; Smith BS
    Q J Med; 1972 Oct; 41(164):491-508. PubMed ID: 4636548
    [No Abstract]   [Full Text] [Related]  

  • 4. Idiopathic familial atrial cardiomyopathy with diffuse conduction block.
    Stables RH; Bailey C; Ormerod OJ
    Q J Med; 1989 Apr; 71(264):325-32. PubMed ID: 2594963
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Atrial cardiomyopathy an orphan disease or common disorder?
    Fatkin D; Nikolova-Krstevski V
    Circ Cardiovasc Genet; 2013 Feb; 6(1):5-6. PubMed ID: 23424254
    [No Abstract]   [Full Text] [Related]  

  • 6. Metabolic cardiomyopathy and mitochondrial disorders in the pediatric intensive care unit.
    Kane JM; Rossi J; Tsao S; Burton BK
    J Pediatr; 2007 Nov; 151(5):538-41. PubMed ID: 17961702
    [No Abstract]   [Full Text] [Related]  

  • 7. Torsade de pontes and complete heart block in familial cardiomyopathy.
    Tan AT; Ee BK; Chia BL
    Singapore Med J; 1984 Apr; 25(2):84-6. PubMed ID: 6474209
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. [The electrocardiogram in myocardial diseases].
    Hess OM; Krayenbühl HP
    Schweiz Med Wochenschr; 1982 Mar; 112(10):333-8. PubMed ID: 6210957
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Contribution of genetics to cardiomyopathy].
    Komajda M
    Bull Acad Natl Med; 2002; 186(1):31-42; discussion 42-3. PubMed ID: 12146140
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Obstructive cardiomyopathy. Intraventricular conduction disorders and profuse lentiginosis. Genetic cardiocutaneous syndromes].
    Pernot C; Henry M; Worms AM
    Coeur Med Interne; 1972; 11(2):249-57. PubMed ID: 5049024
    [No Abstract]   [Full Text] [Related]  

  • 12. Familial cardiomyopathy associated with right bundle branch block, ST segment elevation and sudden death.
    Fontaine G
    J Am Coll Cardiol; 1996 Aug; 28(2):540-1. PubMed ID: 8800140
    [No Abstract]   [Full Text] [Related]  

  • 13. A case of familial atrioventricular heart block affected by alteration of the autonomic nervous system.
    Takehara N; Kawamura Y; Sato N; Sato A; Kakuchi H; Kikuchi K
    J Electrocardiol; 2001 Oct; 34(4):339-44. PubMed ID: 11590576
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Familial idiopathic cardiomyopathy].
    Petrov D
    Vutr Boles; 1982; 21(4):96-9. PubMed ID: 7147927
    [No Abstract]   [Full Text] [Related]  

  • 15. Intrahisian block in cardiomyopathy.
    Rakovec P; Pust B
    Cor Vasa; 1984; 26(6):438-44. PubMed ID: 6543166
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial conduction system disease associated with hypertrophic cardiomyopathy.
    Bahl A; Saikia UN; Talwar KK
    Int J Cardiol; 2008 Apr; 125(3):e44-7. PubMed ID: 17445920
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Electrophysiological and histopathological characteristics of progressive atrioventricular block accompanied by familial dilated cardiomyopathy caused by a novel mutation of lamin A/C gene.
    Otomo J; Kure S; Shiba T; Karibe A; Shinozaki T; Yagi T; Naganuma H; Tezuka F; Miura M; Ito M; Watanabe J; Matsubara Y; Shirato K
    J Cardiovasc Electrophysiol; 2005 Feb; 16(2):137-45. PubMed ID: 15720451
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Hereditary cardiomyopathies: a review. Mutation of structural proteins a common cause of hereditary cardiomyopathy].
    Sjöberg G; Kostareva A; Sejersen T
    Lakartidningen; 2005 Mar 14-20; 102(11):845-7, 850-3. PubMed ID: 15835520
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Familial auriculo-ventricular heart block?].
    Grondin P; Nguyen HV; Malcolm I
    Can Med Assoc J; 1983 May; 128(10):1144. PubMed ID: 6839235
    [No Abstract]   [Full Text] [Related]  

  • 20. [Familial heart block].
    Winter M
    Orv Hetil; 1981 Oct; 122(43):2647-9. PubMed ID: 7322561
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.