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Author Greco S |
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Article
Aguilar-Gonzalez A ; Gonzalez-Correa JE ; Barriocanal-Casado E ; Ramos-Hernandez I ; Lerma-Juarez MA ; Greco S ; Rodriguez-Sevilla JJ ; Molina-Estevez FJ ; Montalvo-Romeral V ; Ronzitti G ; Sanchez-Martin RM ; Martin F ; Munoz P | 04/06/2022Article
Perfetti A, Author ; Greco S ; Cardani R ; Fossati B ; Cuomo G ; Valaperta R ; Ambrogi F ; Cortese A ; Botta A ; Mignarri A ; Santoro M ; Gaetano C ; Costa E ; Dotti MT ; Silvestri G ; Massa R ; Meola G ; Martelli F | 2016Article
Perfetti A, Author ; Greco S, Author ; Fasanaro P, Author ; Bugiardini E, Author ; Cardani R, Author ; Garcia Manteiga JM, Author ; Riba M, Author ; Citarro D, Author ; Stupka E, Author ; Meola G, Author ; Martelli F, Author | 04/2014Article
Perfetti A ; Greco S ; Bugiardini E ; Cardani R ; Gaia P ; Gaetano C ; Meola G ; Martelli F | 2014Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Cardani R ; Greco S ; Sarra-Ferraris G ; Bugiardini E ; Meola G ; Martelli F | 2011Myotonic dystrophy type 1(DM1) is a dominantly inherited multisystemic disorder affecting skeletal muscle, heart, eye, and the endocrine system. DM1 is caused by expansion of a CTG repeat in the 3'UTR of DMPK gene. This genetic lesion leads to t[...]