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

Year Number of Results
2003 2
2005 1
2008 2
2009 2
2010 2
2011 5
2013 1
2014 1
2016 1
2018 1
2020 1
2022 1
2023 2
2024 0

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20 results

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Page 1
qPCR Applications for the Determination of the Biological Age.
Castagnetta M, Pfeffer U, Chiesa A, Gennaro E, Cecconi M, Coviello D, Sacchi N. Castagnetta M, et al. Among authors: cecconi m. Methods Mol Biol. 2020;2065:191-197. doi: 10.1007/978-1-4939-9833-3_14. Methods Mol Biol. 2020. PMID: 31578696
Significance of sarcomere gene mutations analysis in the end-stage phase of hypertrophic cardiomyopathy.
Biagini E, Olivotto I, Iascone M, Parodi MI, Girolami F, Frisso G, Autore C, Limongelli G, Cecconi M, Maron BJ, Maron MS, Rosmini S, Formisano F, Musumeci B, Cecchi F, Iacovoni A, Haas TS, Bacchi Reggiani ML, Ferrazzi P, Salvatore F, Spirito P, Rapezzi C. Biagini E, et al. Among authors: cecconi m. Am J Cardiol. 2014 Sep 1;114(5):769-76. doi: 10.1016/j.amjcard.2014.05.065. Epub 2014 Jun 19. Am J Cardiol. 2014. PMID: 25037680
Targeted next-generation sequencing helps to decipher the genetic and phenotypic heterogeneity of hypertrophic cardiomyopathy.
Cecconi M, Parodi MI, Formisano F, Spirito P, Autore C, Musumeci MB, Favale S, Forleo C, Rapezzi C, Biagini E, Davì S, Canepa E, Pennese L, Castagnetta M, Degiorgio D, Coviello DA. Cecconi M, et al. Int J Mol Med. 2016 Oct;38(4):1111-24. doi: 10.3892/ijmm.2016.2732. Epub 2016 Sep 7. Int J Mol Med. 2016. PMID: 27600940 Free PMC article.
Perlman syndrome: clinical report and nine-year follow-up.
Piccione M, Cecconi M, Giuffrè M, Lo Curto M, Malacarne M, Piro E, Riccio A, Corsello G. Piccione M, et al. Among authors: cecconi m. Am J Med Genet A. 2005 Dec 1;139A(2):131-5. doi: 10.1002/ajmg.a.30994. Am J Med Genet A. 2005. PMID: 16278893
No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy.
Madia F, Gennaro E, Cecconi M, Buti D, Capovilla G, Dalla Bernardina B, Elia M, Ferrari A, Fontana E, Gaggero R, Giannotta M, Giordano L, Granata T, La Selva L, Luisa Lispi M, Santucci M, Vanadia F, Veggiotti P, Vigliano P, Viri M, Dagna Bricarelli F, Bianchi A, Zara F. Madia F, et al. Among authors: cecconi m. Epilepsy Res. 2003 Mar;53(3):196-200. doi: 10.1016/s0920-1211(03)00022-6. Epilepsy Res. 2003. PMID: 12694927
Deletion of NSD1 exon 14 in Sotos syndrome: first description.
Piccione M, Consiglio V, Di Fiore A, Grasso M, Cecconi M, Perroni L, Corsello G. Piccione M, et al. Among authors: cecconi m. J Genet. 2011 Apr;90(1):119-23. doi: 10.1007/s12041-011-0017-6. J Genet. 2011. PMID: 21677396 Free article. No abstract available.
20 results