CERMINARA, MARIA
CERMINARA, MARIA
100009 - Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno-Infantili
Complex cases with Autism Spectrum Disorder (ASD), developmental delay, hyperactivity and sleep disturbance explained by oligogenic mechanisms
2021-01-01 Cerminara, Maria; Servetti, Martina; Squillari2, Margherita; Pisciotta, Livia; Spirito, Giovanni; Teresa Divizia, Maria; Lerone, Margherita; DE GRANDIS, Elisa; Boeri, Silvia; Nobili, Lino; Vozzi, Diego; Sanges, Remo; Zara, Federico; Gustincich, Stefano; Puliti, Aldamaria
In-vitro and in-vivo studies depict metabotropic glutamate receptor 5 as a potential pharmacological target to modulate disease progression in ALS
2021-01-01 Milanese, M.; Torazza, C.; Provenzano, F.; Bonifacino, T.; Ravera, S.; Balbi, M.; Frumento, G.; Kumar, M.; Cerminara, M.; Puliti, A.; Usai, C.; Bonanno, G.
Partial deletion of mGluR5 affects microglia inflammatory phenotype, bioenergetic characteristics, and red-ox state during ALS progression in SOD1G93A mice
2022-01-01 Balbi, Matilde; Bonifacino, T.; Ravera, Silvia; Fenoglio, D.; Altosole, T.; Filaci, G.; Leardi, R.; Farinini, E.; Cerminara, M.; Puliti, Aldamaria; Milanese, Marco; Bonanno, G.
Phenotypic spectrum overview of patients with neurodevelopmental disorders sharing one recurrent copy number variant (CNV) and carrying different additional CNVs
2022-01-01 Servetti, Martina; Pisciotta, Livia; Tassano, Elisa; Cerminara, Maria; Fontana, Marco; Bagliani, Chiara; Nobili, Lino; Boeri, Silvia; Rosti, Giulia; Lerone, Margherita; Teresa Divizia, Maria; Zara, Federico; Ronchetto, Patrizia; Puliti, Aldamaria
Phenotypic Spectrum revealed by two hits model mechanism in Neurodevelopmental Disorder patients with Syndromic and Recurrent CNVs.
2021-01-01 Servetti, M.; Pisciotta, L.; Tassano, E.; Cerminara, M.; Nobili, L.; Boeri, S.; Rosti, G.; Lerone, M.; Divizia, M. T.; Zara, F.; Ronchetto, P.; Puliti, A.
Relevance of double-hit mechanisms in patients with Neurodevelopmental Disorders (NDDs): a re-evaluation of 526 patients with non-benign copy number variants (CNVs).
2021-01-01 Servetti, Martina; Pisciotta, Livia; Tassano, Elisa; Nobili, Lino; Boeri, Silvia; Cerminara, Maria; Lerone, Margherita; Teresa Divizia, Maria; Ronchetto, Patrizia; Puliti, Aldamaria
Whole exome sequencing (WES) and functional analyses suggest synergistic effects of deleterious variants in two candidate genes for Poland Syndrome
2022-01-01 Cerminara, Maria; Vaccari, Carlotta; Musante, Ilaria; Divizia, MARIA TERESA; Lerone, Margherita; Torre, Michele; Victoria Romanini, Maria; Bossi, Simone; Servetti, Martina; Bocciardi, Renata; Pedemonte, Nicoletta; Del Zotto, Genny; Maria Senes, Filippo; Valle, Maura; Grazia Calevo, Maria; Fontana, Marco; Cittaro, Davide; Lazarevic, Dejan; Zara, Federico; Francesca Bedeschi, Maria; Puliti, Aldamaria
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Complex cases with Autism Spectrum Disorder (ASD), developmental delay, hyperactivity and sleep disturbance explained by oligogenic mechanisms | 1-gen-2021 | Cerminara, Maria; Servetti, Martina; Squillari2, Margherita; Pisciotta, Livia; Spirito, Giovanni; Teresa Divizia, Maria; Lerone, Margherita; DE GRANDIS, Elisa; Boeri, Silvia; Nobili, Lino; Vozzi, Diego; Sanges, Remo; Zara, Federico; Gustincich, Stefano; Puliti, Aldamaria | |
| In-vitro and in-vivo studies depict metabotropic glutamate receptor 5 as a potential pharmacological target to modulate disease progression in ALS | 1-gen-2021 | Milanese, M.; Torazza, C.; Provenzano, F.; Bonifacino, T.; Ravera, S.; Balbi, M.; Frumento, G.; Kumar, M.; Cerminara, M.; Puliti, A.; Usai, C.; Bonanno, G. | |
| Partial deletion of mGluR5 affects microglia inflammatory phenotype, bioenergetic characteristics, and red-ox state during ALS progression in SOD1G93A mice | 1-gen-2022 | Balbi, Matilde; Bonifacino, T.; Ravera, Silvia; Fenoglio, D.; Altosole, T.; Filaci, G.; Leardi, R.; Farinini, E.; Cerminara, M.; Puliti, Aldamaria; Milanese, Marco; Bonanno, G. | |
| Phenotypic spectrum overview of patients with neurodevelopmental disorders sharing one recurrent copy number variant (CNV) and carrying different additional CNVs | 1-gen-2022 | Servetti, Martina; Pisciotta, Livia; Tassano, Elisa; Cerminara, Maria; Fontana, Marco; Bagliani, Chiara; Nobili, Lino; Boeri, Silvia; Rosti, Giulia; Lerone, Margherita; Teresa Divizia, Maria; Zara, Federico; Ronchetto, Patrizia; Puliti, Aldamaria | |
| Phenotypic Spectrum revealed by two hits model mechanism in Neurodevelopmental Disorder patients with Syndromic and Recurrent CNVs. | 1-gen-2021 | Servetti, M.; Pisciotta, L.; Tassano, E.; Cerminara, M.; Nobili, L.; Boeri, S.; Rosti, G.; Lerone, M.; Divizia, M. T.; Zara, F.; Ronchetto, P.; Puliti, A. | |
| Relevance of double-hit mechanisms in patients with Neurodevelopmental Disorders (NDDs): a re-evaluation of 526 patients with non-benign copy number variants (CNVs). | 1-gen-2021 | Servetti, Martina; Pisciotta, Livia; Tassano, Elisa; Nobili, Lino; Boeri, Silvia; Cerminara, Maria; Lerone, Margherita; Teresa Divizia, Maria; Ronchetto, Patrizia; Puliti, Aldamaria | |
| Whole exome sequencing (WES) and functional analyses suggest synergistic effects of deleterious variants in two candidate genes for Poland Syndrome | 1-gen-2022 | Cerminara, Maria; Vaccari, Carlotta; Musante, Ilaria; Divizia, MARIA TERESA; Lerone, Margherita; Torre, Michele; Victoria Romanini, Maria; Bossi, Simone; Servetti, Martina; Bocciardi, Renata; Pedemonte, Nicoletta; Del Zotto, Genny; Maria Senes, Filippo; Valle, Maura; Grazia Calevo, Maria; Fontana, Marco; Cittaro, Davide; Lazarevic, Dejan; Zara, Federico; Francesca Bedeschi, Maria; Puliti, Aldamaria |