Sfoglia per Autore
7p22.1 microduplication syndrome : clinical and molecular characterization of an adult case and review of the literature
2015 R. Caselli, L. Ballarati, A. Vignoli, A. Peron, M.P. Recalcati, I. Catusi, L. Larizza, D. Giardino
iPSC-derived neurons of CREBBP- and EP300-mutated Rubinstein-Taybi syndrome patients show morphological alterations and hypoexcitability
2018 V. Alari, S. Russo, B. Terragni, P.F. Ajmone, A. Sironi, I. Catusi, L. Calzari, D. Concolino, R. Marotta, D. Milani, D. Giardino, M. Mantegazza, C. Gervasini, P. Finelli, L. Larizza
13q mosaic deletion including RB1 associated to mild phenotype and no cancer outcome-case report and review of the literature
2018 I. Bestetti, A. Sironi, I. Catusi, M. Mariani, D. Giardino, S. Manoukian, D. Milani, L. Larizza, C. Castronovo, P. Finelli
Instability of short arm of acrocentric chromosomes : Lesson from non-acrocentric satellited chromosomes. Report of 24 unrelated cases
2020 S. Redaelli, D. Conconi, N. Villa, E. Sala, F. Crosti, C. Corti, I. Catusi, M. Garzo, L. Romitti, E. Martinoli, A. Patrizi, R. Malgara, M.P. Recalcati, L. Dalprà, M. Lavitrano, P. Riva, G. Roversi, A. Bentivegna
Ring Chromosome 20 Syndrome : Genetics, Clinical Characteristics, and Overlapping Phenotypes
2020 A. Peron, I. Catusi, M.P. Recalcati, L. Calzari, L. Larizza, A. Vignoli, M.P. Canevini
Histone deacetylase inhibitors ameliorate morphological defects and hypoexcitability of iPSC-neurons from Rubinstein-Taybi patients
2021 V. Alari, P. Scalmani, P.F. Ajmone, S. Perego, S. Avignone, I. Catusi, P.A. Lonati, M.O. Borghi, P. Finelli, B. Terragni, M. Mantegazza, S. Russo, L. Larizza
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile