MANTOVANI, VALENTINA
MANTOVANI, VALENTINA
DIPARTIMENTO DI MEDICINA SPECIALISTICA, DIAGNOSTICA E SPERIMENTALE (attivo dal 28/10/2011 al 31/12/2022)
HNF1B-related syndrome: genotype-phenotype correlation
2020 Cristalli, Cp; Mattiaccio, A; Graziano, C; Capelli, I; Baraldi, O; Comai, G; Pariali, M; Gargano, L; Seri, M; La Manna, G; Mantovani, V
Genetic and viral characterization by high throughput mass spectrometry in kidney transplant recipients
2018 Cristalli, Cp; Mucciacciaro, V; De Carolis, S; Mattiaccio, A; Minardi, R; Ruggeri, M; Comai, G; Cricca, M; Bonafe, M; Mantovani, V; La Manna, G
Genetic heterogeneity in nephronophthisis and related syndromes
2018 Minardi, R; Cristalli, Cp; Mattiaccio, A; Pariali, M; Baraldi, O; Capelli, I; Comai, G; Graziano, C; Seri, M; La Manna, G; Mantovani, V
Non-valvular atrial fibrillation: Potential clinical implications of the heterogeneous definitions used in trials on new oral anticoagulants
2015 Boriani, Giuseppe; Cimaglia, Paolo; Fantecchi, Elisa; Mantovani, Valentina; Ziacchi, Matteo; Valzania, Cinzia; Martignani, Cristian; Biffi, Mauro; Diemberger, Igor
Corrigendum: Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients(EMBO Mol Med, (2014), 6, (795–809), 10.1002/emmm.201303235)
2014 Bonora, E.; Graziano, C.; Minopoli, F.; Bacchelli, E.; Magini, P.; Diquigiovanni, C.; Lomartire, S.; Bianco, F.; Vargiolu, M.; Parchi, P.; Marasco, E.; Mantovani, V.; Rampoldi, L.; Trudu, M.; Parmeggiani, A.; Battaglia, A.; Mazzone, L.; Tortora, G.; Maestrini, E.; Seri, M.; Romeo, G.
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| HNF1B-related syndrome: genotype-phenotype correlation | Cristalli, Cp; Mattiaccio, A; Graziano, C; Capelli, I; Baraldi, O; Comai, G; Pariali, M; Gargano,... L; Seri, M; La Manna, G; Mantovani, V | 2020-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 4.01 Contributo in Atti di convegno | - |
| Genetic and viral characterization by high throughput mass spectrometry in kidney transplant recipients | Cristalli, Cp; Mucciacciaro, V; De Carolis, S; Mattiaccio, A; Minardi, R; Ruggeri, M; Comai, G; C...ricca, M; Bonafe, M; Mantovani, V; La Manna, G | 2018-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 4.01 Contributo in Atti di convegno | - |
| Genetic heterogeneity in nephronophthisis and related syndromes | Minardi, R; Cristalli, Cp; Mattiaccio, A; Pariali, M; Baraldi, O; Capelli, I; Comai, G; Graziano,... C; Seri, M; La Manna, G; Mantovani, V | 2018-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 4.01 Contributo in Atti di convegno | - |
| Non-valvular atrial fibrillation: Potential clinical implications of the heterogeneous definitions used in trials on new oral anticoagulants | Boriani, Giuseppe; Cimaglia, Paolo; Fantecchi, Elisa; Mantovani, Valentina; Ziacchi, Matteo; Valz...ania, Cinzia; Martignani, Cristian; Biffi, Mauro; Diemberger, Igor | 2015-01-01 | JOURNAL OF CARDIOVASCULAR MEDICINE | - | 1.01 Articolo in rivista | - |
| Corrigendum: Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients(EMBO Mol Med, (2014), 6, (795–809), 10.1002/emmm.201303235) | Bonora, E.; Graziano, C.; Minopoli, F.; Bacchelli, E.; Magini, P.; Diquigiovanni, C.; Lomartire, ...S.; Bianco, F.; Vargiolu, M.; Parchi, P.; Marasco, E.; Mantovani, V.; Rampoldi, L.; Trudu, M.; Parmeggiani, A.; Battaglia, A.; Mazzone, L.; Tortora, G.; Maestrini, E.; Seri, M.; Romeo, G. | 2014-01-01 | EMBO MOLECULAR MEDICINE | - | 1.01 Articolo in rivista | - |