Early manifestations in a cohort of children prenatally diagnosed with 47,XYY. Role of multidisciplinary counseling for parental guidance and prevention of aggressive behavior

por Lalatta, Faustina, Folliero, Emanuela, Cavallari, Ugo, Di Segni, Marina, Gentilin, Barbara, Fogliani, Roberto, Quagliarini, Donatella, Vizziello, Paola, Monti, Federico, Gargantini, Luigi
Publicado 2012

Derivation of human induced pluripotent stem cell line EURACi004-A from skin fibroblasts of a patient with Arrhythmogenic Cardiomyopathy carrying the heterozygous PKP2 mutation c.2...

por Ermon, Benedetta, Volpato, Claudia B., Cattelan, Giada, Silipigni, Rosamaria, Di Segni, Marina, Cantaloni, Chiara, Casella, Michela, Pramstaller, Peter P., Pompilio, Giulio, Sommariva, Elena, Meraviglia, Viviana, Rossini, Alessandra
Publicado 2018

Generation of the Becker muscular dystrophy patient derived induced pluripotent stem cell line carrying the DMD splicing mutation c.1705-8 T>C.

por Rovina, Davide, Castiglioni, Elisa, Niro, Francesco, Farini, Andrea, Belicchi, Marzia, Di Fede, Elisabetta, Gervasini, Cristina, Paganini, Stefania, Di Segni, Marina, Torrente, Yvan, Santoro, Rosaria, Pompilio, Giulio, Gowran, Aoife
Publicado 2020