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.
157 related articles for article (PubMed ID: 20978592)
1. Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy. Otten E; Lekanne Dit Deprez RH; Weiss MM; van Slegtenhorst M; Joosten M; van der Smagt JJ; de Jonge N; Kerstjens-Frederikse WS; Roofthooft MT; Balk AH; van den Berg MP; Ruiter JS; van Tintelen JP Neth Heart J; 2010 Oct; 18(10):478-85. PubMed ID: 20978592 [TBL] [Abstract][Full Text] [Related]
2. Genotype-specific pathogenic effects in human dilated cardiomyopathy. Bollen IAE; Schuldt M; Harakalova M; Vink A; Asselbergs FW; Pinto JR; Krüger M; Kuster DWD; van der Velden J J Physiol; 2017 Jul; 595(14):4677-4693. PubMed ID: 28436080 [TBL] [Abstract][Full Text] [Related]
3. Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy. Mogensen J; Murphy RT; Shaw T; Bahl A; Redwood C; Watkins H; Burke M; Elliott PM; McKenna WJ J Am Coll Cardiol; 2004 Nov; 44(10):2033-40. PubMed ID: 15542288 [TBL] [Abstract][Full Text] [Related]
4. Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy. Petropoulou E; Soltani M; Firoozabadi AD; Namayandeh SM; Crockford J; Maroofian R; Jamshidi Y Eur J Med Genet; 2017 Sep; 60(9):485-488. PubMed ID: 28642161 [TBL] [Abstract][Full Text] [Related]
5. Familial dilated cardiomyopathy with troponin T K210del mutation. Martins E; Silva-Cardoso J; Alves C; Pereira H; Soares B; Damasceno A; Abreu-Lima C; Amorim A; Rocha-Gonçalves F Rev Port Cardiol; 2006 Mar; 25(3):295-300. PubMed ID: 16789403 [TBL] [Abstract][Full Text] [Related]
6. Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death. Fernlund E; Österberg AW; Kuchinskaya E; Gustafsson M; Jansson K; Gunnarsson C Pediatr Cardiol; 2017 Aug; 38(6):1262-1268. PubMed ID: 28669108 [TBL] [Abstract][Full Text] [Related]
7. The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy. Ahmad F; Banerjee SK; Lage ML; Huang XN; Smith SH; Saba S; Rager J; Conner DA; Janczewski AM; Tobita K; Tinney JP; Moskowitz IP; Perez-Atayde AR; Keller BB; Mathier MA; Shroff SG; Seidman CE; Seidman JG PLoS One; 2008 Jul; 3(7):e2642. PubMed ID: 18612386 [TBL] [Abstract][Full Text] [Related]
8. Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene. Villard E; Duboscq-Bidot L; Charron P; Benaiche A; Conraads V; Sylvius N; Komajda M Eur Heart J; 2005 Apr; 26(8):794-803. PubMed ID: 15769782 [TBL] [Abstract][Full Text] [Related]
9. Clinical and Prognostic Profiles of Cardiomyopathies Caused by Mutations in the Troponin T Gene. Ripoll-Vera T; Gámez JM; Govea N; Gómez Y; Núñez J; Socías L; Escandell Á; Rosell J Rev Esp Cardiol (Engl Ed); 2016 Feb; 69(2):149-58. PubMed ID: 26507537 [TBL] [Abstract][Full Text] [Related]
10. Hypertrophic cardiomyopathy: low frequency of mutations in the beta-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients. García-Castro M; Reguero JR; Batalla A; Díaz-Molina B; González P; Alvarez V; Cortina A; Cubero GI; Coto E Clin Chem; 2003 Aug; 49(8):1279-85. PubMed ID: 12881443 [TBL] [Abstract][Full Text] [Related]
11. Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience. van Spaendonck-Zwarts KY; van Rijsingen IA; van den Berg MP; Lekanne Deprez RH; Post JG; van Mil AM; Asselbergs FW; Christiaans I; van Langen IM; Wilde AA; de Boer RA; Jongbloed JD; Pinto YM; van Tintelen JP Eur J Heart Fail; 2013 Jun; 15(6):628-36. PubMed ID: 23349452 [TBL] [Abstract][Full Text] [Related]
12. Cardiac troponin T (TNNT2) mutations in chinese dilated cardiomyopathy patients. Li X; Luo R; Gu H; Deng Y; Xu X; Wu X; Hua W Biomed Res Int; 2014; 2014():907360. PubMed ID: 25110706 [TBL] [Abstract][Full Text] [Related]
13. Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy. van den Wijngaard A; Volders P; Van Tintelen JP; Jongbloed JD; van den Berg MP; Lekanne Deprez RH; Mannens MM; Hofmann N; Slegtenhorst M; Dooijes D; Michels M; Arens Y; Jongbloed R; Smeets BJ Neth Heart J; 2011 Aug; 19(7-8):344-51. PubMed ID: 21533915 [TBL] [Abstract][Full Text] [Related]
14. Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system. Zhao Y; Cao H; Song Y; Feng Y; Ding X; Pang M; Zhang Y; Zhang H; Ding J; Xia X Int J Mol Med; 2016 Jun; 37(6):1511-20. PubMed ID: 27082122 [TBL] [Abstract][Full Text] [Related]
15. Late onset sporadic dilated cardiomyopathy caused by a cardiac troponin T mutation. Morales A; Pinto JR; Siegfried JD; Li D; Norton N; Hofmeyer M; Vallin M; Morales AR; Potter JD; Hershberger RE Clin Transl Sci; 2010 Oct; 3(5):219-26. PubMed ID: 20973921 [TBL] [Abstract][Full Text] [Related]
16. Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy. Merlo M; Sinagra G; Carniel E; Slavov D; Zhu X; Barbati G; Spezzacatene A; Ramani F; Salcedo E; Di Lenarda A; Mestroni L; Taylor MR; Clin Transl Sci; 2013 Dec; 6(6):424-8. PubMed ID: 24119082 [TBL] [Abstract][Full Text] [Related]
17. Prevalence and Phenotypic Expression of Mutations in the MYH7, MYBPC3 and TNNT2 Genes in Families with Hypertrophic Cardiomyopathy in the South of Brazil: A Cross-Sectional Study. Mattos BP; Scolari FL; Torres MA; Simon L; Freitas VC; Giugliani R; Matte Ú Arq Bras Cardiol; 2016 Sep; 107(3):257-265. PubMed ID: 27737317 [TBL] [Abstract][Full Text] [Related]
19. Troponin T amino acid mutation (ΔK210) knock-in mice as a neonatal dilated cardiomyopathy model. Tanihata J; Fujii T; Baba S; Fujimoto Y; Morimoto S; Minamisawa S Pediatr Res; 2021 Mar; 89(4):846-857. PubMed ID: 32563186 [TBL] [Abstract][Full Text] [Related]
20. A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy. Girolami F; Olivotto I; Passerini I; Zachara E; Nistri S; Re F; Fantini S; Baldini K; Torricelli F; Cecchi F J Cardiovasc Med (Hagerstown); 2006 Aug; 7(8):601-7. PubMed ID: 16858239 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]