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Page 1
Obliterated cavum septi pellucidi: Clinical significance and role of fetal magnetic resonance.
Fantasia I, Ciardo C, Bracalente G, Filippi E, Murru FM, Spezzacatene A, Bin M, Mendez Quintero O, Montaguti E, Lees C, Papanikolaou K, Pilu G, Prefumo F, Thilaganathan B, Stampalija T. Fantasia I, et al. Among authors: spezzacatene a. Acta Obstet Gynecol Scand. 2023 Jun;102(6):744-750. doi: 10.1111/aogs.14575. Epub 2023 Apr 14. Acta Obstet Gynecol Scand. 2023. PMID: 37059118 Free PMC article.
Giant non-parasitic mixed splenic cyst in a child.
Cleva M, Vaivoda A, Boscarelli A, Codrich D, Spezzacatene A, Murru FM. Cleva M, et al. Among authors: spezzacatene a. J Paediatr Child Health. 2023 Jan;59(1):175-177. doi: 10.1111/jpc.16220. Epub 2022 Sep 20. J Paediatr Child Health. 2023. PMID: 36124936 No abstract available.
Right precordial-directed electrocardiographical markers identify arrhythmogenic right ventricular cardiomyopathy in the absence of conventional depolarization or repolarization abnormalities.
Cortez D, Svensson A, Carlson J, Graw S, Sharma N, Brun F, Spezzacatene A, Mestroni L, Platonov PG. Cortez D, et al. Among authors: spezzacatene a. BMC Cardiovasc Disord. 2017 Oct 13;17(1):261. doi: 10.1186/s12872-017-0696-x. BMC Cardiovasc Disord. 2017. PMID: 29029613 Free PMC article.
Role of Titin Missense Variants in Dilated Cardiomyopathy.
Begay RL, Graw S, Sinagra G, Merlo M, Slavov D, Gowan K, Jones KL, Barbati G, Spezzacatene A, Brun F, Di Lenarda A, Smith JE, Granzier HL, Mestroni L, Taylor M; Familial Cardiomyopathy Registry. Begay RL, et al. Among authors: spezzacatene a. J Am Heart Assoc. 2015 Nov 13;4(11):e002645. doi: 10.1161/JAHA.115.002645. J Am Heart Assoc. 2015. PMID: 26567375 Free PMC article.
Arrhythmogenic Phenotype in Dilated Cardiomyopathy: Natural History and Predictors of Life-Threatening Arrhythmias.
Spezzacatene A, Sinagra G, Merlo M, Barbati G, Graw SL, Brun F, Slavov D, Di Lenarda A, Salcedo EE, Towbin JA, Saffitz JE, Marcus FI, Zareba W, Taylor MR, Mestroni L; Familial Cardiomyopathy Registry. Spezzacatene A, et al. J Am Heart Assoc. 2015 Oct 16;4(10):e002149. doi: 10.1161/JAHA.115.002149. J Am Heart Assoc. 2015. PMID: 26475296 Free PMC article.
GENETIC CAUSES OF DILATED CARDIOMYOPATHY.
Mestroni L, Brun F, Spezzacatene A, Sinagra G, Taylor MR. Mestroni L, et al. Among authors: spezzacatene a. Prog Pediatr Cardiol. 2014 Dec;37(1-2):13-18. doi: 10.1016/j.ppedcard.2014.10.003. Prog Pediatr Cardiol. 2014. PMID: 25584016 Free PMC article.
Titin and desmosomal genes in the natural history of arrhythmogenic right ventricular cardiomyopathy.
Brun F, Barnes CV, Sinagra G, Slavov D, Barbati G, Zhu X, Graw SL, Spezzacatene A, Pinamonti B, Merlo M, Salcedo EE, Sauer WH, Taylor MR, Mestroni L; Familial Cardiomyopathy Registry. Brun F, et al. Among authors: spezzacatene a. J Med Genet. 2014 Oct;51(10):669-76. doi: 10.1136/jmedgenet-2014-102591. Epub 2014 Aug 25. J Med Genet. 2014. PMID: 25157032 Free PMC article.
Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
Merlo M, Sinagra G, Carniel E, Slavov D, Zhu X, Barbati G, Spezzacatene A, Ramani F, Salcedo E, Di Lenarda A, Mestroni L, Taylor MR; Familial Cardiomyopathy Registry. Merlo M, et al. Among authors: spezzacatene a. Clin Transl Sci. 2013 Dec;6(6):424-8. doi: 10.1111/cts.12116. Epub 2013 Oct 3. Clin Transl Sci. 2013. PMID: 24119082 Free PMC article.