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Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis.
Te Riele AS, Agullo-Pascual E, James CA, Leo-Macias A, Cerrone M, Zhang M, Lin X, Lin B, Sobreira NL, Amat-Alarcon N, Marsman RF, Murray B, Tichnell C, van der Heijden JF, Dooijes D, van Veen TA, Tandri H, Fowler SJ, Hauer RN, Tomaselli G, van den Berg MP, Taylor MR, Brun F, Sinagra G, Wilde AA, Mestroni L, Bezzina CR, Calkins H, Peter van Tintelen J, Bu L, Delmar M, Judge DP. Te Riele AS, et al. Among authors: mestroni l. Cardiovasc Res. 2017 Jan;113(1):102-111. doi: 10.1093/cvr/cvw234. Cardiovasc Res. 2017. PMID: 28069705 Free PMC article.
Genetic factors in dilated cardiomyopathy.
Mestroni L, Milasin J, Vatta M, Pinamonti B, Sinagra G, Rocco C, Matulic M, Falaschi A, Giacca M, Camerini F. Mestroni L, et al. Arch Mal Coeur Vaiss. 1996 Jul;89 Spec No 2:15-20. Arch Mal Coeur Vaiss. 1996. PMID: 8881501 Review.
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. Among authors: mestroni l. 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.
Cardiology patient page. Familial dilated cardiomyopathy.
Ku L, Feiger J, Taylor M, Mestroni L; Familial Cardiomyopathy Registry. Ku L, et al. Among authors: mestroni l. Circulation. 2003 Oct 28;108(17):e118-21. doi: 10.1161/01.CIR.0000097493.70422.50. Circulation. 2003. PMID: 14581388 No abstract available.
260 results