المؤلفون: Corti, Claudia (ORCID 0000-0003-1466-3182), Oldrati, Viola, Storm, Fabio, Bardoni, Alessandra, Strazzer, Sandra, Romaniello, Romina

المصدر: Journal of Intellectual Disabilities. Sep 2023 27(3):808-841.

تمت مراجعته من قبل الزملاء: Y

Page Count: 34

الواصفات: Brain, Neurological Impairments, Genetic Disorders, Distance Education, Cognitive Development, Cognitive Ability, Compliance (Psychology), Difficulty Level, Cognitive Processes, Educational Technology, Children, Training, Adolescents, Program Effectiveness

المؤلفون: Ferrari, Elisabetta (ORCID 0000-0002-4781-1367), Butti, Niccolò, Gagliardi, Chiara, Romaniello, Romina, Borgatti, Renato, Urgesi, Cosimo

المصدر: Journal of Autism and Developmental Disorders. Sep 2023 53(9):3343-3355.

تمت مراجعته من قبل الزملاء: Y

Page Count: 13

الواصفات: Patients, Intellectual Disability, Developmental Disabilities, Congenital Impairments, Cognitive Processes, Predictor Variables, Brain, Theory of Mind, Spatial Ability, Visual Acuity, Verbal Ability

المؤلفون: Masnada, Silvia, Pichiecchio, Anna, Formica, Manuela, Arrigoni, Filippo, Borrelli, Paola, Accorsi, Patrizia, Bonanni, Paolo, Borgatti, Renato, Bernardina, Bernardo Dalla, Danieli, Alberto, Darra, Francesca, Deconinck, Nicolas, De Giorgis, Valentina, Dulac, Olivier, Gataullina, Svetlana, Giordano, Lucio, Guerrini, Renzo, La Briola, Francesca, Mastrangelo, Massimo, Montomoli, Martino, Mortilla, Marzia, Osanni, Elisa, Parisi, Pasquale, Perucca, Emilio, Pinelli, Lorenzo, Romaniello, Romina, Severino, Mariasavina, Vigevano, Federico, Vignoli, Aglaia, Bahi-Buisson, Nadia, Cavallin, Mara, Accogli, Andrea, Burgeois, Marie, Capra, Valeria, Chaves-Vischer, Virgine, Chiapparini, Luisa, Colafati, GiovannaStefania, D'Arrigo, Stefano, Desguerre, Isabelle, Doco-Fenzy, Martine, d'Orsi, Giuseppe, Epitashvili, Nino, Fazzi, Elisa, Ferretti, Alessandro, Fiorini, Elena, Fradin, Melanie, Fusco, Carlo, Granata, Tiziana, Johannesen, Katrine Marie, Lebon, Sebastien, Loget, Philippe, Moller, Rikke Steensjerre, Montanaro, Domenico, Orcesi, Simona, Quelin, Chloe, Rebessi, Erika, Romeo, Antonino, Solazzi, Roberta, Spagnoli, Carlotta, Uebler, Christian, Zara, Federico, Arzimanoglou, Alexis, Veggiotti, Pierangelo

المساهمون: Masnada, Silvia, Pichiecchio, Anna, Formica, Manuela, Arrigoni, Filippo, Borrelli, Paola, Accorsi, Patrizia, Bonanni, Paolo, Borgatti, Renato, Bernardina, Bernardo Dalla, Danieli, Alberto, Darra, Francesca, Deconinck, Nicola, De Giorgis, Valentina, Dulac, Olivier, Gataullina, Svetlana, Giordano, Lucio, Guerrini, Renzo, La Briola, Francesca, Mastrangelo, Massimo, Montomoli, Martino, Mortilla, Marzia, Osanni, Elisa, Parisi, Pasquale, Perucca, Emilio, Pinelli, Lorenzo, Romaniello, Romina, Severino, Mariasavina, Vigevano, Federico, Vignoli, Aglaia, Bahi-Buisson, Nadia, Cavallin, Mara, Accogli, Andrea, Burgeois, Marie, Capra, Valeria, Chaves-Vischer, Virgine, Chiapparini, Luisa, Colafati, Giovannastefania, D'Arrigo, Stefano, Desguerre, Isabelle, Doco-Fenzy, Martine, D'Orsi, Giuseppe, Epitashvili, Nino, Fazzi, Elisa, Ferretti, Alessandro, Fiorini, Elena, Fradin, Melanie, Fusco, Carlo, Granata, Tiziana, Johannesen, Katrine Marie, Lebon, Sebastien, Loget, Philippe, Moller, Rikke Steensjerre, Montanaro, Domenico, Orcesi, Simona, Quelin, Chloe, Rebessi, Erika, Romeo, Antonino, Solazzi, Roberta, Spagnoli, Carlotta, Uebler, Christian, Zara, Federico, Arzimanoglou, Alexi, Veggiotti, Pierangelo

مصطلحات موضوعية: Adolescent, Adult, Aicardi Syndrome, Basal Ganglia, Brain, Child, Preschool, Drinking, Drug Resistant Epilepsy, Eating, Electroencephalography, Female, Human, Infant, Magnetic Resonance Imaging, Motor Skill, Retina, Retrospective Studie, Seizure, Treatment Outcome, Young Adult

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33277420; info:eu-repo/semantics/altIdentifier/wos/WOS:000657054500016; volume:96; issue:9; firstpage:e1319; lastpage:e1333; numberofpages:15; journal:NEUROLOGY; http://hdl.handle.net/11564/742291Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85102538218; https://n.neurology.org/content/96/9/e1319.longTest

الإتاحة: https://doi.org/10.1212/WNL.0000000000011237Test
http://hdl.handle.net/11564/742291Test
https://n.neurology.org/content/96/9/e1319.longTest

المؤلفون: Masnada, Silvia, Pichiecchio, Anna, Formica, Manuela, Arrigoni, Filippo, Borrelli, Paola, Accorsi, Patrizia, Bonanni, Paolo, Borgatti, Renato, Dalla Bernardina, Bernardo, Danieli, Alberto, Darra, Francesca, Deconinck, Nicolas, De Giorgis, Valentina, Dulac, Olivier, Gataullina, Svetlana, Giordano, Lucio, Guerrini, Renzo, La Briola, Francesca, Mastrangelo, Massimo, Montomoli, Martino, Mortilla, Marzia, Osanni, Elisa, Parisi, Pasquale, Perucca, Emilio, Pinelli, Lorenzo, Romaniello, Romina, Severino, Mariasavina, Vigevano, Federico, Vignoli, Aglaia, Bahi-Buisson, Nadia, Cavallin, Mara, Accogli, Andrea, Burgeois, Marie, Capra, Valeria, Chaves-Vischer, Virgine, Chiapparini, Luisa, Colafati, GiovannaStefania, D'Arrigo, Stefano, Desguerre, Isabelle, Doco-Fenzy, Martine, D'Orsi, Giuseppe, Epitashvili, Nino, Fazzi, Elisa, Ferretti, Alessandro, Fiorini, Elena, Fradin, Melanie, Fusco, Carlo, Granata, Tiziana, Johannesen, Katrine Marie, Lebon, Sebastien, Loget, Philippe, Moller, Rikke Steensjerre, Montanaro, Domenico, Orcesi, Simona, Quelin, Chloe, Rebessi, Erika, Romeo, Antonino, Solazzi, Roberta, Spagnoli, Carlotta, Uebler, Christian, Zara, Federico, Arzimanoglou, Alexis, Veggiotti, Pierangelo, Grp, Aicardi Syndrome Int Study

المصدر: Neurology
Masnada, S, Pichiecchio, A, Formica, M, Arrigoni, F, Borrelli, P, Accorsi, P, Bonanni, P, Borgatti, R, Dalla Bernardina, B, 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 & Grp, A S I S 2021, ' Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome ', Neurology, vol. 96, no. 9, pp. e1319-e1333 . https://doi.org/10.1212/WNL.0000000000011237Test

مصطلحات موضوعية: 0301 basic medicine, Drug Resistant Epilepsy, Basal Ganglia, Dysmorphism, Aicardi Syndrome, brain malformation, Aicardi Syndrome/diagnostic imaging, Electroencephalography, Corpus callosum, Epilepsy, Eating, 0302 clinical medicine, Basal ganglia, Child, medicine.diagnostic_test, Brain, Magnetic Resonance Imaging, Treatment Outcome, Motor Skills, Brain/abnormalities, Child, Preschool, Female, Radiology, Adult, medicine.medical_specialty, Adolescent, Seizures/diagnostic imaging, Drinking, Basal ganglia dysmorphism, Retina, Article, Aicardi syndrome, 03 medical and health sciences, Young Adult, Basal Ganglia/abnormalities, Neuroimaging, Seizures, medicine, Humans, Preschool, Drug Resistant Epilepsy/diagnostic imaging, Retrospective Studies, Infant, business.industry, Magnetic resonance imaging, Cortical dysplasia, medicine.disease, 030104 developmental biology, Retina/diagnostic imaging, Neurology (clinical), business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c93a062109ebf7072dcc9a86203a9ab3Test
https://pubmed.ncbi.nlm.nih.gov/33277420Test

المؤلفون: Arrigoni, Filippo, Romaniello, Romina, Peruzzo, Denis, Righini, Andrea, Parazzini, Cecilia, Colombo, Paola, Bassi, Maria Teresa, Triulzi, Fabio, Borgatti, Renato

المساهمون: Arrigoni, Filippo, Romaniello, Romina, Peruzzo, Deni, Righini, Andrea, Parazzini, Cecilia, Colombo, Paola, Bassi, Maria Teresa, Triulzi, Fabio, Borgatti, Renato

مصطلحات موضوعية: Brain, Corpus callosum, Diffusion tensor imaging, Intellectual disability, Magnetic resonance imaging, Agenesis of Corpus Callosum, Female, Human, Male, Phenotype

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26560723; volume:26; issue:8; firstpage:2587; lastpage:2596; numberofpages:10; journal:EUROPEAN RADIOLOGY; http://hdl.handle.net/11571/1372016Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84946763350; https://link.springer.com/article/10.1007/s00330-015-4084-6Test

الإتاحة: https://doi.org/10.1007/s00330-015-4084-6Test
http://hdl.handle.net/11571/1372016Test

المؤلفون: Romaniello, Romina, Arrigoni, Filippo, Bassi, Maria Teresa, Borgatti, Renato

المساهمون: Romaniello, Romina, Arrigoni, Filippo, Bassi, Maria Teresa, Borgatti, Renato

مصطلحات موضوعية: Brain malformation, Epilepsy, Genotype–phenotype correlation, Malformations of cortical development, Mental retardation, Tubulin gene, Brain, Human, Nervous System Malformation, Tubulin

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/25008804; volume:37; issue:3; firstpage:273; lastpage:280; numberofpages:8; journal:BRAIN & DEVELOPMENT; http://hdl.handle.net/11571/1372005Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84930902538; https://www.sciencedirect.com/science/article/pii/S0387760414001375?via=ihubTest

الإتاحة: https://doi.org/10.1016/j.braindev.2014.06.002Test
http://hdl.handle.net/11571/1372005Test
https://www.sciencedirect.com/science/article/pii/S0387760414001375?via=ihubTest

المؤلفون: Romaniello, Romina, Saettini, Francesco, Panzeri, Elena, Arrigoni, Filippo, Bassi, Maria T, Borgatti, Renato

المساهمون: Romaniello, Romina, Saettini, Francesco, Panzeri, Elena, Arrigoni, Filippo, Bassi, Maria T, Borgatti, Renato

مصطلحات موضوعية: Brain, Child, Epilepsy, Female, Human, Munc18 Protein, Phenotype, Rett Syndrome, Mutation, Missense

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/25714420; volume:26; issue:5; firstpage:254; lastpage:257; numberofpages:4; journal:NEUROREPORT; http://hdl.handle.net/11571/1372007Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84924973227; https://journals.lww.com/neuroreport/Fulltext/2015/03020/A_de_novo_STXBP1_gene_mutation_in_a_patient.5.aspxTest

الإتاحة: https://doi.org/10.1097/WNR.0000000000000337Test
http://hdl.handle.net/11571/1372007Test
https://journals.lww.com/neuroreport/Fulltext/2015/03020/A_de_novo_STXBP1_gene_mutation_in_a_patient.5.aspxTest

المؤلفون: Colombo, Paola, Borgatti, Renato

المساهمون: Arrigoni, Filippo, Romaniello, Romina, Peruzzo, Deni, Righini, Andrea, Parazzini, Cecilia, Colombo, Paola, Bassi, Maria Teresa, Triulzi, Fabio, Borgatti, Renato

مصطلحات موضوعية: Brain, Corpus callosum, Diffusion tensor imaging, Intellectual disability, Magnetic resonance imaging, Radiology, Nuclear Medicine and Imaging, Settore M-PSI/08 - PSICOLOGIA CLINICA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26560723; info:eu-repo/semantics/altIdentifier/wos/WOS:000379192500020; volume:26; issue:8; firstpage:2587; lastpage:2596; numberofpages:10; issueyear:2016; journal:EUROPEAN RADIOLOGY; http://hdl.handle.net/10807/134525Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84946763350; www.link.springer.de/link/service/journals/00330/index.htm

الإتاحة: https://doi.org/10.1007/s00330-015-4084-6Test
http://hdl.handle.net/10807/134525Test