VACCARI, CARLOTTA
VACCARI, CARLOTTA
Albuminuria and glomerular damage in mice lacking the Metabotropic Glutamate Receptor Type 1 (GRM1).
2011-01-01 Puliti, Aldamaria; Rossi, Pia; Caridi, G; Corbelli, A; Ikehata, M; Armelloni, S; Li, M; Zennaro, C; Conti, V; Vaccari, Carlotta; Cassanello, M; Calevo, Mg; Emionite, L; Ravazzolo, Roberto; Rastaldi, M. P.
De novo deletion of chromosome 11q12.3 in monozygotic twins affected by Poland Syndrome
2014-01-01 Vaccari, Carlotta; Romanini, Mv; Musante, Ilaria; Tassano, E; Gimelli, S; Divizia, Mt; Torre, M; Morovic, Cg; Lerone, M; Ravazzolo, Roberto; Puliti, Aldamaria
Poland syndrome: A proposed classification system and perspectives on diagnosis and treatment
2018-01-01 Romanini, Maria Victoria; Calevo, Maria Grazia; Puliti, Aldamaria; Vaccari, Carlotta; Valle, Maura; Senes, Filippo; Torre, Michele
Thrombocytopenia-absent radius (TAR) syndrome due to compound inheritance for a 1q21.1 microdeletion and a low-frequency noncoding RBM8A SNP: a new familial case
2015-01-01 Tassano, Elisa; Gimelli, Stefania; Divizia, Maria Teresa; Lerone, Margherita; Vaccari, Carlotta; Puliti, Aldamaria; Gimelli, Giorgio
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Albuminuria and glomerular damage in mice lacking the Metabotropic Glutamate Receptor Type 1 (GRM1). | 1-gen-2011 | Puliti, Aldamaria; Rossi, Pia; Caridi, G; Corbelli, A; Ikehata, M; Armelloni, S; Li, M; Zennaro, C; Conti, V; Vaccari, Carlotta; Cassanello, M; Calevo, Mg; Emionite, L; Ravazzolo, Roberto; Rastaldi, M. P. | |
| De novo deletion of chromosome 11q12.3 in monozygotic twins affected by Poland Syndrome | 1-gen-2014 | Vaccari, Carlotta; Romanini, Mv; Musante, Ilaria; Tassano, E; Gimelli, S; Divizia, Mt; Torre, M; Morovic, Cg; Lerone, M; Ravazzolo, Roberto; Puliti, Aldamaria | |
| Poland syndrome: A proposed classification system and perspectives on diagnosis and treatment | 1-gen-2018 | Romanini, Maria Victoria; Calevo, Maria Grazia; Puliti, Aldamaria; Vaccari, Carlotta; Valle, Maura; Senes, Filippo; Torre, Michele | |
| Thrombocytopenia-absent radius (TAR) syndrome due to compound inheritance for a 1q21.1 microdeletion and a low-frequency noncoding RBM8A SNP: a new familial case | 1-gen-2015 | Tassano, Elisa; Gimelli, Stefania; Divizia, Maria Teresa; Lerone, Margherita; Vaccari, Carlotta; Puliti, Aldamaria; Gimelli, Giorgio |