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Page 1
Clinical Features and Natural History of Preadolescent Nonsyndromic Hypertrophic Cardiomyopathy.
Norrish G, Cleary A, Field E, Cervi E, Boleti O, Ziółkowska L, Olivotto I, Khraiche D, Limongelli G, Anastasakis A, Weintraub R, Biagini E, Ragni L, Prendiville T, Duignan S, McLeod K, Ilina M, Fernandez A, Marrone C, Bökenkamp R, Baban A, Kubus P, Daubeney PEF, Sarquella-Brugada G, Cesar S, Klaassen S, Ojala TH, Bhole V, Medrano C, Uzun O, Brown E, Gran F, Sinagra G, Castro FJ, Stuart G, Yamazawa H, Barriales-Villa R, Garcia-Guereta L, Adwani S, Linter K, Bharucha T, Gonzales-Lopez E, Siles A, Rasmussen TB, Calcagnino M, Jones CB, De Wilde H, Kubo T, Felice T, Popoiu A, Mogensen J, Mathur S, Centeno F, Reinhardt Z, Schouvey S, Elliott PM, Kaski JP. Norrish G, et al. Among authors: sinagra g. J Am Coll Cardiol. 2022 May 24;79(20):1986-1997. doi: 10.1016/j.jacc.2022.03.347. J Am Coll Cardiol. 2022. PMID: 35589160 Free PMC article.
Long-term effects of carvedilol in idiopathic dilated cardiomyopathy with persistent left ventricular dysfunction despite chronic metoprolol. The Heart-Muscle Disease Study Group.
Di Lenarda A, Sabbadini G, Salvatore L, Sinagra G, Mestroni L, Pinamonti B, Gregori D, Ciani F, Muzzi A, Klugmann S, Camerini F. Di Lenarda A, et al. Among authors: sinagra g. J Am Coll Cardiol. 1999 Jun;33(7):1926-34. doi: 10.1016/s0735-1097(99)00134-5. J Am Coll Cardiol. 1999. PMID: 10362195 Free article. 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. Among authors: sinagra g. 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.
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: sinagra g. 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.
The Italian Registry for hypertrophic cardiomyopathy: a nationwide survey.
Cecchi F, Olivotto I, Betocchi S, Rapezzi C, Conte MR, Sinagra G, Zachara E, Gavazzi A, Rordorf R, Carnemolla G, Porcu M, Nistri S, Gruppillo P, Giampaoli S. Cecchi F, et al. Among authors: sinagra g. Am Heart J. 2005 Nov;150(5):947-54. doi: 10.1016/j.ahj.2005.01.005. Am Heart J. 2005. PMID: 16290970
SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism.
McNair WP, Sinagra G, Taylor MR, Di Lenarda A, Ferguson DA, Salcedo EE, Slavov D, Zhu X, Caldwell JH, Mestroni L; Familial Cardiomyopathy Registry Research Group. McNair WP, et al. Among authors: sinagra g. J Am Coll Cardiol. 2011 May 24;57(21):2160-8. doi: 10.1016/j.jacc.2010.09.084. J Am Coll Cardiol. 2011. PMID: 21596231 Free PMC article.
971 results