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: Politano, Davide, D'Abrusco, Fulvio, Pasca, Ludovica, Ferraro, Francesca, Gana, Simone, Garau, Jessica, Zanaboni, Martina Paola, Rognone, Elisa, Pichiecchio, Anna, Borgatti, Renato, Valente, Enza Maria, De Giorgis, Valentina, Romaniello, Romina

المصدر: American Journal of Medical Genetics Part A ; volume 194, issue 6 ; ISSN 1552-4825 1552-4833

الإتاحة: https://doi.org/10.1002/ajmg.a.63555Test

المؤلفون: Oldrati, Viola, Butti, Niccolò, Ferrari, Elisabetta, Strazzer, Sandra, Romaniello, Romina, Borgatti, Renato, Urgesi, Cosimo, Finisguerra, Alessandra

المساهمون: Ministero della Salute, Ministero dell'Istruzione dell'Universita e della Ricerca

المصدر: NeuroImage: Clinical ; volume 41, page 103582 ; ISSN 2213-1582

مصطلحات موضوعية: Cognitive Neuroscience, Neurology (clinical), Neurology, Radiology, Nuclear Medicine and imaging

الإتاحة: https://doi.org/10.1016/j.nicl.2024.103582Test
https://api.elsevier.com/content/article/PII:S2213158224000214?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S2213158224000214?httpAccept=text/plainTest

المؤلفون: Serpieri, Valentina, Mortarini, Giulia, Loucks, Hailey, Biagini, Tommaso, Micalizzi, Alessia, Palmieri, Ilaria, Dempsey, Jennifer C, D'Abrusco, Fulvio, Mazzotta, Concetta, Battini, Roberta, Bertini, Enrico Silvio, Boltshauser, Eugen, Borgatti, Renato, Brockmann, Knut, D'Arrigo, Stefano, Nardocci, Nardo, Fischetto, Rita, Agolini, Emanuele, Novelli, Antonio, Romano, Alfonso, Romaniello, Romina, Stanzial, Franco, Signorini, Sabrina, Strisciuglio, Pietro, Gana, Simone, Mazza, Tommaso, Doherty, Dan, Valente, Enza Maria

المساهمون: Serpieri, Valentina, Mortarini, Giulia, Loucks, Hailey, Biagini, Tommaso, Micalizzi, Alessia, Palmieri, Ilaria, Dempsey, Jennifer C, D'Abrusco, Fulvio, Mazzotta, Concetta, Battini, Roberta, Bertini, Enrico Silvio, Boltshauser, Eugen, Borgatti, Renato, Brockmann, Knut, D'Arrigo, Stefano, Nardocci, Nardo, Fischetto, Rita, Agolini, Emanuele, Novelli, Antonio, Romano, Alfonso, Romaniello, Romina, Stanzial, Franco, Signorini, Sabrina, Strisciuglio, Pietro, Gana, Simone, Mazza, Tommaso, Doherty, Dan, Valente, Enza Maria

مصطلحات موضوعية: Cerebellar Disease, Founder Effect, Gene Frequency, Genetic Carrier Screening, Genotype

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36788019; info:eu-repo/semantics/altIdentifier/wos/WOS:000935563200001; numberofpages:14; journal:JOURNAL OF MEDICAL GENETICS; https://hdl.handle.net/11568/1170047Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85159312262; https://jmg.bmj.com/content/60/9/885Test

الإتاحة: https://doi.org/10.1136/jmg-2022-108725Test
https://hdl.handle.net/11568/1170047Test
https://jmg.bmj.com/content/60/9/885Test

المؤلفون: Corti, Claudia, Oldrati, Viola, Papini, Marta, Strazzer, Sandra, Poggi, Geraldina, Romaniello, Romina, Borgatti, Renato, Urgesi, Cosimo, Bardoni, Alessandra

المساهمون: Ministero della Salute

المصدر: Scientific Reports ; volume 13, issue 1 ; ISSN 2045-2322

مصطلحات موضوعية: Multidisciplinary

الإتاحة: https://doi.org/10.1038/s41598-023-41810-1Test
https://www.nature.com/articles/s41598-023-41810-1.pdfTest
https://www.nature.com/articles/s41598-023-41810-1Test

المؤلفون: Cunha, Paulina, Petit, Emilien, Coutelier, Marie, Coarelli, Giulia, Mariotti, Caterina, Faber, Jennifer, Van Gaalen, Judith, Damasio, Joana, Fleszar, Zofia, Tosi, Michele, Rocca, Clarissa, De Michele, Giovanna, Minnerop, Martina, Ewenczyk, Claire, Santorelli, Filippo M., Heinzmann, Anna, Bird, Thomas, Amprosi, Matthias, Indelicato, Elisabetta, Benussi, Alberto, Charles, Perrine, Stendel, Claudia, Romano, Silvia, Scarlato, Marina, Le Ber, Isabelle, Bassi, Maria Teresa, Serrano, Mercedes, Schmitz-Hübsch, Tanja, Doss, Sarah, Van Velzen, Gijs A.J., Thomas, Quentin, Trabacca, Antonio, Ortigoza-Escobar, Juan Dario, D'Arrigo, Stefano, Timmann, Dagmar, Pantaleoni, Chiara, Martinuzzi, Andrea, Besse-Pinot, Elsa, Marsili, Luca, Cioffi, Ettore, Nicita, Francesco, Giorgetti, Alejandro, Moroni, Isabella, Romaniello, Romina, Casali, Carlo, Ponger, Penina, Casari, Giorgio, De Bot, Susanne T., Ristori, Giovanni, Blumkin, Lubov

المصدر: The American Journal of Human Genetics ; volume 110, issue 7, page 1098-1109 ; ISSN 0002-9297

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1016/j.ajhg.2023.05.009Test
https://api.elsevier.com/content/article/PII:S0002929723001660?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0002929723001660?httpAccept=text/plainTest

المؤلفون: Pasca, Ludovica, Politano, Davide, Cavallini, Anna, Panzeri, Elena, Vigone, Maria Cristina, Baldoli, Cristina, Abbate, Marco, Kullmann, Gaia, Marelli, Susan, Pozzobon, Gabriella, Vincenzi, Gaia, Nacinovich, Renata, Bassi, Maria Teresa, Romaniello, Romina

المصدر: Neuropediatrics; Jun2024, Vol. 55 Issue 3, p191-195, 5p

مصطلحات موضوعية: AGENESIS of corpus callosum, DYSPLASIA, PHENOTYPES, GENETIC mutation, CONGENITAL hypothyroidism, CORPUS callosum

المؤلفون: Gafner, Michal, Boltshauser, Eugen, D'Abrusco, Fulvio, Battini, Roberta, Romaniello, Romina, D'Arrigo, Stefano, Zanni, Ginevra, Leibovitz, Zvi, Yosovich, Keren, Lerman-Sagie, Tally

المساهمون: Gafner, Michal, Boltshauser, Eugen, D'Abrusco, Fulvio, Battini, Roberta, Romaniello, Romina, D'Arrigo, Stefano, Zanni, Ginevra, Leibovitz, Zvi, Yosovich, Keren, Lerman-Sagie, Tally

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36175354; info:eu-repo/semantics/altIdentifier/wos/WOS:000861541800001; volume:65; issue:4; numberofpages:11; journal:DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY; https://hdl.handle.net/11568/1157845Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85139054526

الإتاحة: https://doi.org/10.1111/dmcn.15419Test
https://hdl.handle.net/11568/1157845Test

المؤلفون: Butti, Niccolò, Oldrati, Viola, Ferrari, Elisabetta, Romaniello, Romina, Gagliardi, Chiara, Borgatti, Renato, Urgesi, Cosimo

المصدر: Cerebellum; Apr2024, Vol. 23 Issue 2, p579-588, 10p

مصطلحات موضوعية: JOUBERT syndrome, HUMAN abnormalities, CEREBELLAR ataxia, CEREBELLUM, INTELLIGENCE levels, MAYER-Rokitansky-Kuster-Hauser syndrome