Towbin JA - Search Results

1

Myocardial infarction, viral infection, and the cytoskeleton final common pathways of a common disease?

Towbin JA, Vatta M. Towbin JA, et al. J Am Coll Cardiol. 2007 Dec 4;50(23):2215-7. doi: 10.1016/j.jacc.2007.08.034. Epub 2007 Nov 19. J Am Coll Cardiol. 2007. PMID: 18061068 Free article. No abstract available.

2

Molecular normalization of dystrophin in the failing left and right ventricle of patients treated with either pulsatile or continuous flow-type ventricular assist devices.

Vatta M, Stetson SJ, Jimenez S, Entman ML, Noon GP, Bowles NE, Towbin JA, Torre-Amione G. Vatta M, et al. Among authors: towbin ja. J Am Coll Cardiol. 2004 Mar 3;43(5):811-7. doi: 10.1016/j.jacc.2003.09.052. J Am Coll Cardiol. 2004. PMID: 14998622 Free article.

3

Nebulette mutations are associated with dilated cardiomyopathy and endocardial fibroelastosis.

Purevjav E, Varela J, Morgado M, Kearney DL, Li H, Taylor MD, Arimura T, Moncman CL, McKenna W, Murphy RT, Labeit S, Vatta M, Bowles NE, Kimura A, Boriek AM, Towbin JA. Purevjav E, et al. Among authors: towbin ja. J Am Coll Cardiol. 2010 Oct 26;56(18):1493-502. doi: 10.1016/j.jacc.2010.05.045. J Am Coll Cardiol. 2010. PMID: 20951326 Free PMC article.

4

Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction.

Vatta M, Mohapatra B, Jimenez S, Sanchez X, Faulkner G, Perles Z, Sinagra G, Lin JH, Vu TM, Zhou Q, Bowles KR, Di Lenarda A, Schimmenti L, Fox M, Chrisco MA, Murphy RT, McKenna W, Elliott P, Bowles NE, Chen J, Valle G, Towbin JA. Vatta M, et al. Among authors: towbin ja. J Am Coll Cardiol. 2003 Dec 3;42(11):2014-27. doi: 10.1016/j.jacc.2003.10.021. J Am Coll Cardiol. 2003. PMID: 14662268 Free article.

5

ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy gene.

Moulik M, Vatta M, Witt SH, Arola AM, Murphy RT, McKenna WJ, Boriek AM, Oka K, Labeit S, Bowles NE, Arimura T, Kimura A, Towbin JA. Moulik M, et al. Among authors: towbin ja. J Am Coll Cardiol. 2009 Jul 21;54(4):325-33. doi: 10.1016/j.jacc.2009.02.076. J Am Coll Cardiol. 2009. PMID: 19608030 Free PMC article.

6

Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathy.

Xu T, Yang Z, Vatta M, Rampazzo A, Beffagna G, Pilichou K, Scherer SE, Saffitz J, Kravitz J, Zareba W, Danieli GA, Lorenzon A, Nava A, Bauce B, Thiene G, Basso C, Calkins H, Gear K, Marcus F, Towbin JA; Multidisciplinary Study of Right Ventricular Dysplasia Investigators. Xu T, et al. Among authors: towbin ja. J Am Coll Cardiol. 2010 Feb 9;55(6):587-97. doi: 10.1016/j.jacc.2009.11.020. J Am Coll Cardiol. 2010. PMID: 20152563 Free PMC article.

7

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome.

Vatta M, Dumaine R, Varghese G, Richard TA, Shimizu W, Aihara N, Nademanee K, Brugada R, Brugada J, Veerakul G, Li H, Bowles NE, Brugada P, Antzelevitch C, Towbin JA. Vatta M, et al. Among authors: towbin ja. Hum Mol Genet. 2002 Feb 1;11(3):337-45. doi: 10.1093/hmg/11.3.337. Hum Mol Genet. 2002. PMID: 11823453

8

Genetics and cardiac arrhythmias.

Towbin JA, Vatta M, Li H, Bowles NE. Towbin JA, et al. Adv Pediatr. 2002;49:87-129. Adv Pediatr. 2002. PMID: 12214781 Review.

9

Beta2-adrenergic receptor genetic variants and risk of sudden cardiac death.

Sotoodehnia N, Siscovick DS, Vatta M, Psaty BM, Tracy RP, Towbin JA, Lemaitre RN, Rea TD, Durda JP, Chang JM, Lumley TS, Kuller LH, Burke GL, Heckbert SR. Sotoodehnia N, et al. Among authors: towbin ja. Circulation. 2006 Apr 18;113(15):1842-8. doi: 10.1161/CIRCULATIONAHA.105.582833. Circulation. 2006. PMID: 16618831

10

Arrhythmogenic right ventricular cardiomyopathy: a 'final common pathway' that defines clinical phenotype.

Vatta M, Marcus F, Towbin JA. Vatta M, et al. Among authors: towbin ja. Eur Heart J. 2007 Mar;28(5):529-30. doi: 10.1093/eurheartj/ehl530. Epub 2007 Feb 15. Eur Heart J. 2007. PMID: 17303588 No abstract available.

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