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: Serpieri, Valentina, D'Abrusco, Fulvio, Dempsey, Jennifer C, Cheng, Yong-Han Hank, Arrigoni, Filippo, Baker, Janice, Battini, Roberta, Bertini, Enrico Silvio, Borgatti, Renato, Christman, Angela K, Curry, Cynthia, D'Arrigo, Stefano, Fluss, Joel, Freilinger, Michael, Gana, Simone, Ishak, Gisele E, Leuzzi, Vincenzo, Loucks, Hailey, Manti, Filippo, Mendelsohn, Nancy, Merlini, Laura, Miller, Caitlin V, Muhammad, Ansar, Nuovo, Sara, Romaniello, Romina, Schmidt, Wolfgang, Signorini, Sabrina, Siliquini, Sabrina, Szczałuba, Krzysztof, Vasco, Gessica, Wilson, Meredith, Zanni, Ginevra, Boltshauser, Eugen, Doherty, Dan, Valente, Enza Maria

المساهمون: Serpieri, Valentina, D'Abrusco, Fulvio, Dempsey, Jennifer C, Cheng, Yong-Han Hank, Arrigoni, Filippo, Baker, Janice, Battini, Roberta, Bertini, Enrico Silvio, Borgatti, Renato, Christman, Angela K, Curry, Cynthia, D'Arrigo, Stefano, Fluss, Joel, Freilinger, Michael, Gana, Simone, Ishak, Gisele E, Leuzzi, Vincenzo, Loucks, Hailey, Manti, Filippo, Mendelsohn, Nancy, Merlini, Laura, Miller, Caitlin V, Muhammad, Ansar, Nuovo, Sara, Romaniello, Romina, Schmidt, Wolfgang, Signorini, Sabrina, Siliquini, Sabrina, Szczałuba, Krzysztof, Vasco, Gessica, Wilson, Meredith, Zanni, Ginevra, Boltshauser, Eugen, Doherty, Dan, Valente, Enza Maria

مصطلحات موضوعية: and neonatal diseases and abnormalitie, central nervous system disease, cerebellar disease, congenital, early diagnosi, genetic variation, hereditary, Cerebellum, Haploinsufficiency, Human, Male, Phenotype, Repressor Protein, Retina, Abnormalities, Multiple, Cerebellar Ataxia, Eye Abnormalitie, Intellectual Disability, Kidney Diseases, Cystic

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34675124; volume:59; issue:9; firstpage:888; lastpage:894; numberofpages:7; journal:EJMG; https://hdl.handle.net/11571/1465615Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85120304902

الإتاحة: https://doi.org/10.1136/jmedgenet-2021-108114Test
https://hdl.handle.net/11571/1465615Test

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, Romina¹, Marelli, Susan¹, Borgatti, Renato¹, Giorda, Roberto², Bassi, Maria T.², Bedeschi, Maria F.³, Bonaglia, Maria C.⁴, Arrigoni, Filippo⁵, Triulzi, Fabio⁵

المصدر: Journal of Child Neurology. Jan2017, Vol. 32 Issue 1, p60-71. 12p.

مصطلحات موضوعية: *AGENESIS of corpus callosum, *BRAIN abnormalities, *INTELLECTUAL disabilities, *COMPARATIVE genomic hybridization, *EPILEPSY

المؤلفون: Borgatti, Renato

المساهمون: Romaniello, Romina, Marelli, Susan, Giorda, Roberto, Bedeschi, Maria F., Bonaglia, Maria C., Arrigoni, Filippo, Triulzi, Fabio, Bassi, Maria T., Borgatti, Renato

مصطلحات موضوعية: array-CGH, brain malformation, corpus callosum, genetic, intellectual disability, Pediatrics, Perinatology and Child Health, Neurology (clinical), Settore M-PSI/08 - PSICOLOGIA CLINICA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27683483; info:eu-repo/semantics/altIdentifier/wos/WOS:000397213000008; volume:32; issue:1; firstpage:60; lastpage:71; numberofpages:12; issueyear:2017; journal:JOURNAL OF CHILD NEUROLOGY; http://hdl.handle.net/10807/134490Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85006413839; http://jcn.sagepub.comTest/

الإتاحة: https://doi.org/10.1177/0883073816664668Test
http://hdl.handle.net/10807/134490Test
http://jcn.sagepub.comTest/

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