ROMANIELLO, ROMINA
ROMANIELLO, ROMINA
DIPARTIMENTO DI MEDICINA MOLECOLARE
A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype
2015-01-01 Romaniello, Romina; Saettini, Francesco; Panzeri, Elena; Arrigoni, Filippo; Bassi, Maria T; Borgatti, Renato
Aberrant supracallosal longitudinal bundle: MR features, pathogenesis and associated clinical phenotype
2016-01-01 Arrigoni, Filippo; Romaniello, Romina; Peruzzo, Denis; Righini, Andrea; Parazzini, Cecilia; Colombo, Paola; Bassi, Maria Teresa; Triulzi, Fabio; Borgatti, Renato
CASK related disorder: Epilepsy and developmental outcome
2021-01-01 Giacomini, T.; Nuovo, S.; Zanni, G.; Mancardi, M. M.; Cusmai, R.; Pepi, C.; Bertini, E.; Valente, E. M.; Battini, R.; Ferrari, A.; Romaniello, R.; Zucca, C.; Borgatti, R.; Uccella, S.; Severino, M.; Striano, P.; Pistorio, A.; Prato, G.; De Grandis, E.; Nobili, L.; Pisciotta, L.
Challenges and resources in adult life with Joubert syndrome: issues from an international classification of functioning (ICF) perspective
2021-01-01 Romaniello, R.; Gagliardi, C.; Desalvo, P.; Provenzi, L.; Battini, R.; Bertini, E.; Bonati, M. T.; Briguglio, M.; D'Arrigo, S.; Dotti, M. T.; Giordano, L.; Macaluso, C.; Moroni, I.; Nuovo, S.; Santucci, M.; Signorini, S.; Stanzial, F.; Valente, E. M.; Borgatti, R.
Characterizingwhite matter tract organization in polymicrogyria and lissencephaly: A multifiber diffusion mri modeling and tractography study
2020-01-01 Arrigoni, F.; Peruzzo, D.; Mandelstam, S.; Amorosino, G.; Redaelli, D.; Romaniello, R.; Leventer, R.; Borgatti, R.; Seal, M.; Yang, J. Y. -M.
Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients with Agenesis of the Corpus Callosum
2017-01-01 Romaniello, R.; Marelli, S.; Giorda, R.; Bedeschi, M. F.; Bonaglia, M. C.; Arrigoni, F.; Triulzi, F.; Bassi, M. T.; Borgatti, R.
Feasibility of a home-based computerized cognitive training for pediatric patients with congenital or acquired brain damage: An explorative study
2018-01-01 Corti, C.; Poggi, G.; Romaniello, R.; Strazzer, S.; Urgesi, C.; Borgatti, R.; Bardoni, A.
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders
2020-01-01 Nicita, F.; Ginevrino, M.; Travaglini, L.; D'Arrigo, S.; Zorzi, G.; Borgatti, R.; Terrone, G.; Catteruccia, M.; Vasco, G.; Brankovic, V.; Siliquini, S.; Romano, S.; Veredice, C.; Pedemonte, M.; Armando, M.; Lettori, D.; Stregapede, F.; Bosco, L.; Sferra, A.; Tessarollo, V.; Romaniello, R.; Ristori, G.; Bertini, E.; Valente, E. M.; Zanni, G.
Learning to live without the cerebellum
2015-01-01 Arrigoni, Filippo; Romaniello, Romina; Nordio, Andrea; Gagliardi, Chiara; Borgatti, Renato
Mutations in α- and β-tubulin encoding genes: implications in brain malformations
2015-01-01 Romaniello, Romina; Arrigoni, Filippo; Bassi, Maria Teresa; Borgatti, Renato
Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: Results of a multicentric study
2020-01-01 Nuovo, S.; Micalizzi, A.; Romaniello, R.; Arrigoni, F.; Ginevrino, M.; Casella, A.; Serpieri, V.; D'Arrigo, S.; Briguglio, M.; Salerno, G. G.; Rossato, S.; Sartori, S.; Leuzzi, V.; Battini, R.; Ben-Zeev, B.; Graziano, C.; Mirabelli Badenier, M.; Brankovic, V.; Nardocci, N.; Spiegel, R.; Petkovic RamadAa, D.; Vento, G.; Marti, I.; Simonati, A.; Dipresa, S.; Freri, E.; Mazza, T.; Bassi, M. T.; Bosco, L.; Travaglini, L.; Zanni, G.; Bertini, E. S.; Vanacore, N.; Borgatti, R.; Valente, E. M.
The phenotypic spectrum of WWOX -related disorders: 20 additional cases of WOREE syndrome and review of the literature
2019-01-01 Piard, J.; Hawkes, L.; Milh, M.; Villard, L.; Borgatti, R.; Romaniello, R.; Fradin, M.; Capri, Y.; Heron, D.; Nougues, M. -C.; Nava, C.; Arsene, O. T.; Shears, D.; Taylor, J.; Pagnamenta, A.; Taylor, J. C.; Sogawa, Y.; Johnson, D.; Firth, H.; Vasudevan, P.; Jones, G.; Nguyen-Morel, M. -A.; Busa, T.; Roubertie, A.; van den Born, M.; Brischoux-Boucher, E.; Koenig, M.; Mignot, C.; Kini, U.; Philippe, C.
Tubulin genes and malformations of cortical development
2018-01-01 Romaniello, R.; Arrigoni, F.; Fry, A. E.; Bassi, M. T.; Rees, M. I.; Borgatti, R.; Pilz, D. T.; Cushion, T. D.
Virtual Reality Social Prediction Improvement and Rehabilitation Intensive Training (VR-SPIRIT) for paediatric patients with congenital cerebellar diseases: Study protocol of a randomised controlled trial
2020-01-01 Butti, N.; Biffi, E.; Genova, C.; Romaniello, R.; Redaelli, D. F.; Reni, G.; Borgatti, R.; Urgesi, C.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype | 1-gen-2015 | Romaniello, Romina; Saettini, Francesco; Panzeri, Elena; Arrigoni, Filippo; Bassi, Maria T; Borgatti, Renato | |
| Aberrant supracallosal longitudinal bundle: MR features, pathogenesis and associated clinical phenotype | 1-gen-2016 | Arrigoni, Filippo; Romaniello, Romina; Peruzzo, Denis; Righini, Andrea; Parazzini, Cecilia; Colombo, Paola; Bassi, Maria Teresa; Triulzi, Fabio; Borgatti, Renato | |
| CASK related disorder: Epilepsy and developmental outcome | 1-gen-2021 | Giacomini, T.; Nuovo, S.; Zanni, G.; Mancardi, M. M.; Cusmai, R.; Pepi, C.; Bertini, E.; Valente, E. M.; Battini, R.; Ferrari, A.; Romaniello, R.; Zucca, C.; Borgatti, R.; Uccella, S.; Severino, M.; Striano, P.; Pistorio, A.; Prato, G.; De Grandis, E.; Nobili, L.; Pisciotta, L. | |
| Challenges and resources in adult life with Joubert syndrome: issues from an international classification of functioning (ICF) perspective | 1-gen-2021 | Romaniello, R.; Gagliardi, C.; Desalvo, P.; Provenzi, L.; Battini, R.; Bertini, E.; Bonati, M. T.; Briguglio, M.; D'Arrigo, S.; Dotti, M. T.; Giordano, L.; Macaluso, C.; Moroni, I.; Nuovo, S.; Santucci, M.; Signorini, S.; Stanzial, F.; Valente, E. M.; Borgatti, R. | |
| Characterizingwhite matter tract organization in polymicrogyria and lissencephaly: A multifiber diffusion mri modeling and tractography study | 1-gen-2020 | Arrigoni, F.; Peruzzo, D.; Mandelstam, S.; Amorosino, G.; Redaelli, D.; Romaniello, R.; Leventer, R.; Borgatti, R.; Seal, M.; Yang, J. Y. -M. | |
| Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients with Agenesis of the Corpus Callosum | 1-gen-2017 | Romaniello, R.; Marelli, S.; Giorda, R.; Bedeschi, M. F.; Bonaglia, M. C.; Arrigoni, F.; Triulzi, F.; Bassi, M. T.; Borgatti, R. | |
| Feasibility of a home-based computerized cognitive training for pediatric patients with congenital or acquired brain damage: An explorative study | 1-gen-2018 | Corti, C.; Poggi, G.; Romaniello, R.; Strazzer, S.; Urgesi, C.; Borgatti, R.; Bardoni, A. | |
| Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders | 1-gen-2020 | Nicita, F.; Ginevrino, M.; Travaglini, L.; D'Arrigo, S.; Zorzi, G.; Borgatti, R.; Terrone, G.; Catteruccia, M.; Vasco, G.; Brankovic, V.; Siliquini, S.; Romano, S.; Veredice, C.; Pedemonte, M.; Armando, M.; Lettori, D.; Stregapede, F.; Bosco, L.; Sferra, A.; Tessarollo, V.; Romaniello, R.; Ristori, G.; Bertini, E.; Valente, E. M.; Zanni, G. | |
| Learning to live without the cerebellum | 1-gen-2015 | Arrigoni, Filippo; Romaniello, Romina; Nordio, Andrea; Gagliardi, Chiara; Borgatti, Renato | |
| Mutations in α- and β-tubulin encoding genes: implications in brain malformations | 1-gen-2015 | Romaniello, Romina; Arrigoni, Filippo; Bassi, Maria Teresa; Borgatti, Renato | |
| Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: Results of a multicentric study | 1-gen-2020 | Nuovo, S.; Micalizzi, A.; Romaniello, R.; Arrigoni, F.; Ginevrino, M.; Casella, A.; Serpieri, V.; D'Arrigo, S.; Briguglio, M.; Salerno, G. G.; Rossato, S.; Sartori, S.; Leuzzi, V.; Battini, R.; Ben-Zeev, B.; Graziano, C.; Mirabelli Badenier, M.; Brankovic, V.; Nardocci, N.; Spiegel, R.; Petkovic RamadAa, D.; Vento, G.; Marti, I.; Simonati, A.; Dipresa, S.; Freri, E.; Mazza, T.; Bassi, M. T.; Bosco, L.; Travaglini, L.; Zanni, G.; Bertini, E. S.; Vanacore, N.; Borgatti, R.; Valente, E. M. | |
| The phenotypic spectrum of WWOX -related disorders: 20 additional cases of WOREE syndrome and review of the literature | 1-gen-2019 | Piard, J.; Hawkes, L.; Milh, M.; Villard, L.; Borgatti, R.; Romaniello, R.; Fradin, M.; Capri, Y.; Heron, D.; Nougues, M. -C.; Nava, C.; Arsene, O. T.; Shears, D.; Taylor, J.; Pagnamenta, A.; Taylor, J. C.; Sogawa, Y.; Johnson, D.; Firth, H.; Vasudevan, P.; Jones, G.; Nguyen-Morel, M. -A.; Busa, T.; Roubertie, A.; van den Born, M.; Brischoux-Boucher, E.; Koenig, M.; Mignot, C.; Kini, U.; Philippe, C. | |
| Tubulin genes and malformations of cortical development | 1-gen-2018 | Romaniello, R.; Arrigoni, F.; Fry, A. E.; Bassi, M. T.; Rees, M. I.; Borgatti, R.; Pilz, D. T.; Cushion, T. D. | |
| Virtual Reality Social Prediction Improvement and Rehabilitation Intensive Training (VR-SPIRIT) for paediatric patients with congenital cerebellar diseases: Study protocol of a randomised controlled trial | 1-gen-2020 | Butti, N.; Biffi, E.; Genova, C.; Romaniello, R.; Redaelli, D. F.; Reni, G.; Borgatti, R.; Urgesi, C. |