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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]
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]