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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 3
1976 5
1977 2
1978 1
1979 3
1980 4
1981 1
1982 2
1983 1
1984 1
1988 2
1989 1
1990 2
1992 2
1993 6
1994 1
1995 1
1996 4
1997 1
1998 1
1999 3
2000 1
2001 1
2003 1
2005 1
2006 1
2007 3
2008 2
2009 2
2010 3
2011 1
2012 1
2013 3
2015 2
2016 1
2017 1
2020 1
2021 1
2022 0
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Search Results

72 results
Results by year
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Page 1
Cardiac findings in congenital muscular dystrophies.
Finsterer J, Ramaciotti C, Wang CH, Wahbi K, Rosenthal D, Duboc D, Melacini P. Finsterer J, et al. Among authors: melacini p. Pediatrics. 2010 Sep;126(3):538-45. doi: 10.1542/peds.2010-0208. Epub 2010 Aug 2. Pediatrics. 2010. PMID: 20679303 Review.
Consensus statement on standard of care for congenital muscular dystrophies.
Wang CH, Bonnemann CG, Rutkowski A, Sejersen T, Bellini J, Battista V, Florence JM, Schara U, Schuler PM, Wahbi K, Aloysius A, Bash RO, Béroud C, Bertini E, Bushby K, Cohn RD, Connolly AM, Deconinck N, Desguerre I, Eagle M, Estournet-Mathiaud B, Ferreiro A, Fujak A, Goemans N, Iannaccone ST, Jouinot P, Main M, Melacini P, Mueller-Felber W, Muntoni F, Nelson LL, Rahbek J, Quijano-Roy S, Sewry C, Storhaug K, Simonds A, Tseng B, Vajsar J, Vianello A, Zeller R; International Standard of Care Committee for Congenital Muscular Dystrophy. Wang CH, et al. Among authors: melacini p. J Child Neurol. 2010 Dec;25(12):1559-81. doi: 10.1177/0883073810381924. Epub 2010 Nov 15. J Child Neurol. 2010. PMID: 21078917 Free PMC article. Review.
Novel Missense Variant in MYL2 Gene Associated With Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology.
De Bortoli M, Vio R, Basso C, Calore M, Minervini G, Angelini A, Melacini P, Vitiello L, Vazza G, Thiene G, Tosatto S, Corrado D, Iliceto S, Rampazzo A, Calore C. De Bortoli M, et al. Among authors: melacini p. Circ Genom Precis Med. 2020 Apr;13(2):e002824. doi: 10.1161/CIRCGEN.119.002824. Epub 2020 Jan 31. Circ Genom Precis Med. 2020. PMID: 32004434 No abstract available.
Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy.
De Bortoli M, Calore C, Lorenzon A, Calore M, Poloni G, Mazzotti E, Rigato I, Marra MP, Melacini P, Iliceto S, Thiene G, Basso C, Daliento L, Corrado D, Rampazzo A, Bauce B. De Bortoli M, et al. Among authors: melacini p. Eur J Hum Genet. 2017 Oct;25(10):1165-1169. doi: 10.1038/ejhg.2017.109. Epub 2017 Jul 12. Eur J Hum Genet. 2017. PMID: 28699631 Free PMC article.
Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies.
Perrot A, Tomasov P, Villard E, Faludi R, Melacini P, Lossie J, Lohmann N, Richard P, De Bortoli M, Angelini A, Varga-Szemes A, Sperling SR, Simor T, Veselka J, Özcelik C, Charron P. Perrot A, et al. Among authors: melacini p. Arch Med Sci. 2016 Apr 1;12(2):263-78. doi: 10.5114/aoms.2016.59250. Epub 2016 Apr 11. Arch Med Sci. 2016. PMID: 27186169 Free PMC article.
No evidence of cardiomyopathy in spinal and bulbar muscular atrophy.
Querin G, Melacini P, D'Ascenzo C, Morandi L, Mazzini L, Silani V, Romito S, Mandrioli J, Raimondi M, Pegoraro E, Soraru' G. Querin G, et al. Among authors: melacini p. Acta Neurol Scand. 2013 Dec;128(6):e30-2. doi: 10.1111/ane.12140. Epub 2013 May 16. Acta Neurol Scand. 2013. PMID: 23679084
Cardioembolic stroke in Danon disease.
Spinazzi M, Fanin M, Melacini P, Nascimbeni AC, Angelini C. Spinazzi M, et al. Among authors: melacini p. Clin Genet. 2008 Apr;73(4):388-90. doi: 10.1111/j.1399-0004.2008.00971.x. Epub 2008 Feb 26. Clin Genet. 2008. PMID: 18312451 No abstract available.
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy.
Barp A, Bello L, Politano L, Melacini P, Calore C, Polo A, Vianello S, Sorarù G, Semplicini C, Pantic B, Taglia A, Picillo E, Magri F, Gorni K, Messina S, Vita GL, Vita G, Comi GP, Ermani M, Calvo V, Angelini C, Hoffman EP, Pegoraro E. Barp A, et al. Among authors: melacini p. PLoS One. 2015 Oct 29;10(10):e0141240. doi: 10.1371/journal.pone.0141240. eCollection 2015. PLoS One. 2015. PMID: 26513582 Free PMC article.
72 results