BORGATTI, RENATO
BORGATTI, RENATO
DIPARTIMENTO DI SCIENZE DEL SISTEMA NERVOSO E DEL COMPORTAMENTO
A 2.3Mb duplication of chromosome 8q24.3 associated with severe mental retardation and epilepsy detected by standard karyotype
2005-01-01 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
2015-01-01 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
2010-01-01 Montirosso, R; Borgatti, R; Trojan, S; Zanini, R; Tronick, E
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
A different brain: Anomalies of functional and structural connections in williams syndrome
2018-01-01 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
2015-01-01 Provenzi, Livio; Borgatti, Renato; Menozzi, Giorgia; Montirosso, Rosario
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation
2004-01-01 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
2012-01-01 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
2011-01-01 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
2010-01-01 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
2016-01-01 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
2020-01-01 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
2020-01-01 Provenzi, L.; Grumi, S.; Borgatti, R.
Anterior Mesencephalic Cap Dysplasia: Novel Brain Stem Malformative Features Associated with Joubert Syndrome
2017-01-01 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
2021-01-01 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
2021-01-01 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.
Behavioral problems in psychotic, clinically high-risk, and non-psychotic adolescent patients
2022-01-01 Rogantini, C.; Provenzi, L.; Borgatti, R.; Mensi, M.; Iorio, M.; Orlandi, M.; Vecchio, A.
Behavioural features of Italian infants and young adults with Williams-Beuren syndrome
2011-01-01 Gagliardi, C; Martelli, S; Tavano, A; Borgatti, R
Bilateral frontoparietal polymicrogyria (BFPP) syndrome secondary to a 16q12.1-q21 chromosome deletion involving GPR56 gene
2009-01-01 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
1996-01-01 Borgatti, R; Tettamanti, A; Piccinelli, P
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. | |
Behavioral problems in psychotic, clinically high-risk, and non-psychotic adolescent patients | 1-gen-2022 | Rogantini, C.; Provenzi, L.; Borgatti, R.; Mensi, M.; Iorio, M.; Orlandi, M.; Vecchio, A. | |
Behavioural features of Italian infants and young adults with Williams-Beuren syndrome | 1-gen-2011 | Gagliardi, C; Martelli, S; Tavano, A; Borgatti, R | |
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 |