BERLOCO, BIANCA
BERLOCO, BIANCA
100009 - Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno-Infantili
Case Report: Whole Exome Sequencing Revealed Disease-Causing Variants in Two Genes in a Patient With Autism Spectrum Disorder, Intellectual Disability, Hyperactivity, Sleep and Gastrointestinal Disturbances
2021-01-01 Cerminara, M.; Spirito, G.; Pisciotta, L.; Squillario, M.; Servetti, M.; Divizia, M. T.; Lerone, M.; Berloco, B.; Boeri, S.; Nobili, L.; Vozzi, D.; Sanges, R.; Gustincich, S.; Puliti, A.
Correction to: Insomnia in Children with Autism Spectrum Disorder: A Cross-Sectional Study on Clinical Correlates and Parental Stress
2023-01-01 Berloco, Bianca; Guerrera, Silvia; Fucà, Elisa; Menghini, Deny; Valeri, Giovanni; Nobili, Lino; Vicari, Stefano
Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development
2019-01-01 Uccella, S.; Accogli, A.; Tortora, D.; Mancardi, M. M.; Nobili, L.; Berloco, B.; Morana, G.; Striano, P.; Capra, V.; Srour, M.; Saint-Martine, C.; Rossi, A.; Severino, M.
PRENATAL DIAGNOSIS OF CORPUS CAL LOSUM AGENESIS WITH ASSOCIATED INTER HEMISPHERIC CYSTS: LONGTERM OUTCOME IN 23 CHILDREN
2018-01-01 Uccella, S.; Berloco, B.; Tortora, D.; Capra, V.; Ravegnani, M.; Paladini, D.; Pastorino, D.; Mancardi, M. M.; Severino, M.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Case Report: Whole Exome Sequencing Revealed Disease-Causing Variants in Two Genes in a Patient With Autism Spectrum Disorder, Intellectual Disability, Hyperactivity, Sleep and Gastrointestinal Disturbances | 1-gen-2021 | Cerminara, M.; Spirito, G.; Pisciotta, L.; Squillario, M.; Servetti, M.; Divizia, M. T.; Lerone, M.; Berloco, B.; Boeri, S.; Nobili, L.; Vozzi, D.; Sanges, R.; Gustincich, S.; Puliti, A. | |
| Correction to: Insomnia in Children with Autism Spectrum Disorder: A Cross-Sectional Study on Clinical Correlates and Parental Stress | 1-gen-2023 | Berloco, Bianca; Guerrera, Silvia; Fucà, Elisa; Menghini, Deny; Valeri, Giovanni; Nobili, Lino; Vicari, Stefano | |
| Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development | 1-gen-2019 | Uccella, S.; Accogli, A.; Tortora, D.; Mancardi, M. M.; Nobili, L.; Berloco, B.; Morana, G.; Striano, P.; Capra, V.; Srour, M.; Saint-Martine, C.; Rossi, A.; Severino, M. | |
| PRENATAL DIAGNOSIS OF CORPUS CAL LOSUM AGENESIS WITH ASSOCIATED INTER HEMISPHERIC CYSTS: LONGTERM OUTCOME IN 23 CHILDREN | 1-gen-2018 | Uccella, S.; Berloco, B.; Tortora, D.; Capra, V.; Ravegnani, M.; Paladini, D.; Pastorino, D.; Mancardi, M. M.; Severino, M. |