BORGATTI, RENATO

BORGATTI, RENATO  

DIPARTIMENTO DI SCIENZE DEL SISTEMA NERVOSO E DEL COMPORTAMENTO  

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Titolo Data di pubblicazione Autore(i) File
A 2.3Mb duplication of chromosome 8q24.3 associated with severe mental retardation and epilepsy detected by standard karyotype 1-gen-2005 Bonaglia, Mc; Giorda, R; Tenconi, R; Pessina, M; Pramparo, T; Borgatti, R; Zuffardi, O
A categorical approach to infants' individual differences during the Still-Face paradigm 1-gen-2015 Montirosso, Rosario; Casini, Erica; Provenzi, Livio; Putnam, Samuel P; Morandi, Francesco; Fedeli, Claudia; Borgatti, Renato
A comparison of dyadic interactions and coping with still-face in healthy pre-term and full-term infants 1-gen-2010 Montirosso, R; Borgatti, R; Trojan, S; Zanini, R; Tronick, E
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
A different brain: Anomalies of functional and structural connections in williams syndrome 1-gen-2018 Gagliardi, C.; Arrigoni, F.; Nordio, A.; De Luca, A.; Peruzzo, D.; Decio, A.; Leemans, A.; Borgatti, R.
A dynamic system analysis of dyadic flexibility and stability across the Face-to-Face Still-Face procedure: application of the State Space Grid 1-gen-2015 Provenzi, Livio; Borgatti, Renato; Menozzi, Giorgia; Montirosso, Rosario
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation 1-gen-2004 Borgatti, R; Zucca, C; Cavallini, A; Ferrario, M; Panzeri, C; Castaldo, P; Soldovieri, Mv; Baschirotto, C; Bresolin, N; Dalla Bernardina, B; Taglialatela, M; Bassi, Mt
A novel mutation in the beta-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance 1-gen-2012 Romaniello, R; Tonelli, A; Arrigoni, F; Baschirotto, C; Triulzi, F; Bresolin, N; Bassi, Mt; Borgatti, R
A Smile Enhances 3-Month-Olds' Recognition of an Individual Face 1-gen-2011 Turati, C; Montirosso, R; Brenna, V; Ferrara, V; Borgatti, R
A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation 1-gen-2010 Romaniello, R; Zucca, C; Tonelli, A; Bonato, S; Baschirotto, C; Zanotta, N; Epifanio, R; Righini, A; Bresolin, N; Bassi, Mt; Borgatti, R
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
Age and sex prevalence estimate of Joubert syndrome in Italy 1-gen-2020 Nuovo, Sara; Bacigalupo, Ilaria; Ginevrino, Monia; Battini, Roberta; Bertini, Enrico; Borgatti, Renato; Casella, Antonella; Micalizzi, Alessia; Nardella, Marta; Romaniello, Romina; Serpieri, Valentina; Zanni, Ginevra; Valente, Enza Maria; Vanacore, Nicola
Alone With the Kids: Tele-Medicine for Children With Special Healthcare Needs During COVID-19 Emergency 1-gen-2020 Provenzi, L.; Grumi, S.; Borgatti, R.
Anterior Mesencephalic Cap Dysplasia: Novel Brain Stem Malformative Features Associated with Joubert Syndrome 1-gen-2017 Arrigoni, F; Romaniello, R; Peruzzo, D; De Luca, A; Parazzini, C; Valente, ENZA MARIA; Borgatti, R; Triulzi, F.
Assessing Family Functioning Before and After an Integrated Multidisciplinary Family Treatment for Adolescents With Restrictive Eating Disorders 1-gen-2021 Mensi, M. M.; Orlandi, M.; Rogantini, C.; Provenzi, L.; Chiappedi, M.; Criscuolo, M.; Castiglioni, M. C.; Zanna, V.; Borgatti, R.
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome 1-gen-2021 Masnada, S.; Pichiecchio, A.; Formica, M.; Arrigoni, F.; Borrelli, P.; Accorsi, P.; Bonanni, P.; Borgatti, R.; Bernardina, B. D.; Danieli, A.; Darra, F.; Deconinck, N.; De Giorgis, V.; Dulac, O.; Gataullina, S.; Giordano, L.; Guerrini, R.; La Briola, F.; Mastrangelo, M.; Montomoli, M.; Mortilla, M.; Osanni, E.; Parisi, P.; Perucca, E.; Pinelli, L.; Romaniello, R.; Severino, M.; Vigevano, F.; Vignoli, A.; Bahi-Buisson, N.; Cavallin, M.; Accogli, A.; Burgeois, M.; Capra, V.; Chaves-Vischer, V.; Chiapparini, L.; Colafati, G.; D'Arrigo, S.; Desguerre, I.; Doco-Fenzy, M.; D'Orsi, G.; Epitashvili, N.; Fazzi, E.; Ferretti, A.; Fiorini, E.; Fradin, M.; Fusco, C.; Granata, T.; Johannesen, K. M.; Lebon, S.; Loget, P.; Moller, R. S.; Montanaro, D.; Orcesi, S.; Quelin, C.; Rebessi, E.; Romeo, A.; Solazzi, R.; Spagnoli, C.; Uebler, C.; Zara, F.; Arzimanoglou, A.; Veggiotti, P.
Bilateral frontoparietal polymicrogyria (BFPP) syndrome secondary to a 16q12.1-q21 chromosome deletion involving GPR56 gene 1-gen-2009 Borgatti, R; Marelli, S; Bernardini, L; Novelli, A; Cavallini, A; Tonelli, A; Bassi, Mt; Dallapiccola, B
Brain injury in a healthy child one year after periureteral injection of Teflon 1-gen-1996 Borgatti, R; Tettamanti, A; Piccinelli, P
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.
Cerebellar Damage Affects Contextual Priors for Action Prediction in Patients with Childhood Brain Tumor 1-gen-2020 Butti, N.; Corti, C.; Finisguerra, A.; Bardoni, A.; Borgatti, R.; Poggi, G.; Urgesi, C.