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Cardiac Remodeling in Subclinical Hypertrophic Cardiomyopathy: The VANISH Randomized Clinical Trial.
Vissing CR, Axelsson Raja A, Day SM, Russell MW, Zahka K, Lever HM, Pereira AC, Colan SD, Margossian R, Murphy AM, Canter C, Bach RG, Wheeler MT, Rossano JW, Owens AT, Benson L, Mestroni L, Taylor MRG, Patel AR, Wilmot I, Thrush P, Soslow JH, Becker JR, Seidman CE, Lakdawala NK, Cirino AL, McMurray JJV, MacRae CA, Solomon SD, Bundgaard H, Orav EJ, Ho CY; Valsartan for Attenuating Disease Evolution in Early Sarcomeric Hypertrophic Cardiomyopathy (VANISH) Investigators. Vissing CR, et al. Among authors: taylor mrg. JAMA Cardiol. 2023 Nov 1;8(11):1083-1088. doi: 10.1001/jamacardio.2023.2808. JAMA Cardiol. 2023. PMID: 37672268 Clinical Trial.
Natural history of dilated cardiomyopathy due to lamin A/C gene mutations.
Taylor MR, Fain PR, Sinagra G, Robinson ML, Robertson AD, Carniel E, Di Lenarda A, Bohlmeyer TJ, Ferguson DA, Brodsky GL, Boucek MM, Lascor J, Moss AC, Li WL, Stetler GL, Muntoni F, Bristow MR, Mestroni L; Familial Dilated Cardiomyopathy Registry Research Group. Taylor MR, et al. J Am Coll Cardiol. 2003 Mar 5;41(5):771-80. doi: 10.1016/s0735-1097(02)02954-6. J Am Coll Cardiol. 2003. PMID: 12628721 Free article.
Cardiomyopathy, familial dilated.
Taylor MR, Carniel E, Mestroni L. Taylor MR, et al. Orphanet J Rare Dis. 2006 Jul 13;1:27. doi: 10.1186/1750-1172-1-27. Orphanet J Rare Dis. 2006. PMID: 16839424 Free PMC article. Review.
Cardiomyopathy and carnitine deficiency.
Amat di San Filippo C, Taylor MR, Mestroni L, Botto LD, Longo N. Amat di San Filippo C, et al. Mol Genet Metab. 2008 Jun;94(2):162-6. doi: 10.1016/j.ymgme.2008.02.002. Epub 2008 Mar 11. Mol Genet Metab. 2008. PMID: 18337137 Free PMC article.
Heart failure and personalized medicine.
Mestroni L, Merlo M, Taylor MR, Camerini F, Sinagra G. Mestroni L, et al. J Cardiovasc Med (Hagerstown). 2011 Jan;12(1):6-12. doi: 10.2459/JCM.0b013e32833e8b0d. J Cardiovasc Med (Hagerstown). 2011. PMID: 20814312 Review.
159 results