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544 results

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Page 1
Cardiomyopathy With Restrictive Physiology in Sickle Cell Disease.
Niss O, Quinn CT, Lane A, Daily J, Khoury PR, Bakeer N, Kimball TR, Towbin JA, Malik P, Taylor MD. Niss O, et al. Among authors: towbin ja. JACC Cardiovasc Imaging. 2016 Mar;9(3):243-52. doi: 10.1016/j.jcmg.2015.05.013. Epub 2016 Feb 17. JACC Cardiovasc Imaging. 2016. PMID: 26897687 Free PMC article. Review.
Myocardial Fas ligand expression increases susceptibility to AZT-induced cardiomyopathy.
Purevjav E, Nelson DP, Varela JJ, Jimenez S, Kearney DL, Sanchez XV, DeFreitas G, Carabello B, Taylor MD, Vatta M, Shearer WT, Towbin JA, Bowles NE. Purevjav E, et al. Among authors: towbin ja. Cardiovasc Toxicol. 2007;7(4):255-63. doi: 10.1007/s12012-007-9004-9. Epub 2007 Oct 18. Cardiovasc Toxicol. 2007. PMID: 17943461
Hypertrophic cardiomyopathy.
Towbin JA. Towbin JA. Pacing Clin Electrophysiol. 2009 Jul;32 Suppl 2:S23-31. doi: 10.1111/j.1540-8159.2009.02381.x. Pacing Clin Electrophysiol. 2009. PMID: 19602159 Review.
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.
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
Purevjav E, Arimura T, Augustin S, Huby AC, Takagi K, Nunoda S, Kearney DL, Taylor MD, Terasaki F, Bos JM, Ommen SR, Shibata H, Takahashi M, Itoh-Satoh M, McKenna WJ, Murphy RT, Labeit S, Yamanaka Y, Machida N, Park JE, Alexander PM, Weintraub RG, Kitaura Y, Ackerman MJ, Kimura A, Towbin JA. Purevjav E, et al. Among authors: towbin ja. Hum Mol Genet. 2012 May 1;21(9):2039-53. doi: 10.1093/hmg/dds022. Epub 2012 Jan 27. Hum Mol Genet. 2012. PMID: 22286171 Free PMC article.
Pediatric cardiomyopathy: importance of genetic and metabolic evaluation.
Kindel SJ, Miller EM, Gupta R, Cripe LH, Hinton RB, Spicer RL, Towbin JA, Ware SM. Kindel SJ, et al. Among authors: towbin ja. J Card Fail. 2012 May;18(5):396-403. doi: 10.1016/j.cardfail.2012.01.017. Epub 2012 Mar 10. J Card Fail. 2012. PMID: 22555271 Free PMC article.
Altered regional cardiac wall mechanics are associated with differential cardiomyocyte calcium handling due to nebulette mutations in preclinical inherited dilated cardiomyopathy.
Maiellaro-Rafferty K, Wansapura JP, Mendsaikhan U, Osinska H, James JF, Taylor MD, Robbins J, Kranias EG, Towbin JA, Purevjav E. Maiellaro-Rafferty K, et al. Among authors: towbin ja. J Mol Cell Cardiol. 2013 Jul;60:151-60. doi: 10.1016/j.yjmcc.2013.04.021. Epub 2013 Apr 28. J Mol Cell Cardiol. 2013. PMID: 23632046 Free PMC article.
Recovery of echocardiographic function in children with idiopathic dilated cardiomyopathy: results from the pediatric cardiomyopathy registry.
Everitt MD, Sleeper LA, Lu M, Canter CE, Pahl E, Wilkinson JD, Addonizio LJ, Towbin JA, Rossano J, Singh RK, Lamour J, Webber SA, Colan SD, Margossian R, Kantor PF, Jefferies JL, Lipshultz SE; Pediatric Cardiomyopathy Registry Investigators. Everitt MD, et al. Among authors: towbin ja. J Am Coll Cardiol. 2014 Apr 15;63(14):1405-13. doi: 10.1016/j.jacc.2013.11.059. Epub 2014 Feb 19. J Am Coll Cardiol. 2014. PMID: 24561146 Free PMC article.
New mechanistic and therapeutic targets for pediatric heart failure: report from a National Heart, Lung, and Blood Institute working group.
Burns KM, Byrne BJ, Gelb BD, Kühn B, Leinwand LA, Mital S, Pearson GD, Rodefeld M, Rossano JW, Stauffer BL, Taylor MD, Towbin JA, Redington AN. Burns KM, et al. Among authors: towbin ja. Circulation. 2014 Jul 1;130(1):79-86. doi: 10.1161/CIRCULATIONAHA.113.007980. Circulation. 2014. PMID: 24982119 Free PMC article. No abstract available.
544 results