Transient Cognitive Impairment in Epilepsy

por Landi, Silvia, Petrucco, Luigi, Sicca, Federico, Ratto, Gian Michele
Publicado 2019

Kir4.1 Dysfunction in the Pathophysiology of Depression: A Systematic Review

por Della Vecchia, Stefania, Marchese, Maria, Santorelli, Filippo Maria, Sicca, Federico
Publicado 2021

Evolution of Epileptiform Activity in Zebrafish by Statistical-Based Integration of Electrophysiology and 2-Photon Ca(2+) Imaging

por Cozzolino, Olga, Sicca, Federico, Paoli, Emanuele, Trovato, Francesco, Santorelli, Filippo M., Ratto, Gian Michele, Marchese, Maria
Publicado 2020

On the Application of Quantitative EEG for Characterizing Autistic Brain: A Systematic Review

por Billeci, Lucia, Sicca, Federico, Maharatna, Koushik, Apicella, Fabio, Narzisi, Antonio, Campatelli, Giulia, Calderoni, Sara, Pioggia, Giovanni, Muratori, Filippo
Publicado 2013

MECP2 duplication phenotype in symptomatic females: report of three further cases

por Novara, Francesca, Simonati, Alessandro, Sicca, Federico, Battini, Roberta, Fiori, Simona, Contaldo, Annarita, Criscuolo, Lucia, Zuffardi, Orsetta, Ciccone, Roberto
Publicado 2014

The Revolution in Migraine Genetics: From Aching Channels Disorders to a Next-Generation Medicine

por Pellacani, Simona, Sicca, Federico, Di Lorenzo, Cherubino, Grieco, Gaetano S., Valvo, Giulia, Cereda, Cristina, Rubegni, Anna, Santorelli, Filippo M.
Publicado 2016

Autism-epilepsy phenotype with macrocephaly suggests PTEN, but not GLIALCAM, genetic screening

por Marchese, Maria, Conti, Valerio, Valvo, Giulia, Moro, Francesca, Muratori, Filippo, Tancredi, Raffaella, Santorelli, Filippo M, Guerrini, Renzo, Sicca, Federico
Publicado 2014

Understanding Spreading Depression from Headache to Sudden Unexpected Death

por Cozzolino, Olga, Marchese, Maria, Trovato, Francesco, Pracucci, Enrico, Ratto, Gian Michele, Buzzi, Maria Gabriella, Sicca, Federico, Santorelli, Filippo M.
Publicado 2018

Electrophysiological features of sleep in children with Kir4.1 channel mutations and Autism–Epilepsy phenotype: a preliminary study

por Cucchiara, Federico, Frumento, Paolo, Banfi, Tommaso, Sesso, Gianluca, Di Galante, Marco, D’Ascanio, Paola, Valvo, Giulia, Sicca, Federico, Faraguna, Ugo
Publicado 2019

An integrated EEG and eye-tracking approach for the study of responding and initiating joint attention in Autism Spectrum Disorders

por Billeci, Lucia, Narzisi, Antonio, Tonacci, Alessandro, Sbriscia-Fioretti, Beatrice, Serasini, Luca, Fulceri, Francesca, Apicella, Fabio, Sicca, Federico, Calderoni, Sara, Muratori, Filippo
Publicado 2017

Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant Zebrafish

por Grone, Brian P., Marchese, Maria, Hamling, Kyla R., Kumar, Maneesh G., Krasniak, Christopher S., Sicca, Federico, Santorelli, Filippo M., Patel, Manisha, Baraban, Scott C.
Publicado 2016

Expanding the clinical and genetic heterogeneity of SPAX5

por Dosi, Claudia, Galatolo, Daniele, Rubegni, Anna, Doccini, Stefano, Pasquariello, Rosa, Nesti, Claudia, Sicca, Federico, Barghigiani, Melissa, Battini, Roberta, Tessa, Alessandra, Santorelli, Filippo M.
Publicado 2020

Temporal lobe connects regression and macrocephaly to autism spectrum disorders

por Valvo, Giulia, Baldini, Sara, Retico, Alessandra, Rossi, Giuseppe, Tancredi, Raffaella, Ferrari, Anna Rita, Calderoni, Sara, Apicella, Fabio, Muratori, Filippo, Santorelli, Filippo Maria, Sicca, Federico
Publicado 2015

Somatic Overgrowth Predisposes to Seizures in Autism Spectrum Disorders

por Valvo, Giulia, Baldini, Sara, Brachini, Francesca, Apicella, Fabio, Cosenza, Angela, Ferrari, Anna Rita, Guerrini, Renzo, Muratori, Filippo, Romano, Maria Francesca, Santorelli, Filippo M., Tancredi, Raffaella, Sicca, Federico
Publicado 2013

Trehalose Treatment in Zebrafish Model of Lafora Disease

por Della Vecchia, Stefania, Ogi, Asahi, Licitra, Rosario, Abramo, Francesca, Nardi, Gabriele, Mero, Serena, Landi, Silvia, Battini, Roberta, Sicca, Federico, Ratto, Gian Michele, Santorelli, Filippo Maria, Marchese, Maria
Publicado 2022

Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy

por Sicca, Federico, Ambrosini, Elena, Marchese, Maria, Sforna, Luigi, Servettini, Ilenio, Valvo, Giulia, Brignone, Maria Stefania, Lanciotti, Angela, Moro, Francesca, Grottesi, Alessandro, Catacuzzeno, Luigi, Baldini, Sara, Hasan, Sonia, D’Adamo, Maria Cristina, Franciolini, Fabio, Molinari, Paola, Santorelli, Filippo M., Pessia, Mauro
Publicado 2016

Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism–epilepsy phenotype

por Ambrosini, Elena, Sicca, Federico, Brignone, Maria S., D'Adamo, Maria C., Napolitano, Carlo, Servettini, Ilenio, Moro, Francesca, Ruan, Yanfei, Guglielmi, Luca, Pieroni, Stefania, Servillo, Giuseppe, Lanciotti, Angela, Valvo, Giulia, Catacuzzeno, Luigi, Franciolini, Fabio, Molinari, Paola, Marchese, Maria, Grottesi, Alessandro, Guerrini, Renzo, Santorelli, Filippo M., Priori, Silvia, Pessia, Mauro
Publicado 2014

Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52

por D’Amore, Angelica, Tessa, Alessandra, Naef, Valentina, Bassi, Maria Teresa, Citterio, Andrea, Romaniello, Romina, Fichi, Gianluca, Galatolo, Daniele, Mero, Serena, Battini, Roberta, Bertocci, Giulia, Baldacci, Jacopo, Sicca, Federico, Gemignani, Federica, Ricca, Ivana, Rubegni, Anna, Hirst, Jennifer, Marchese, Maria, Sahin, Mustafa, Ebrahimi‐Fakhari, Darius, Santorelli, Filippo M.
Publicado 2020

The Diagnostic Approach to Mitochondrial Disorders in Children in the Era of Next-Generation Sequencing: A 4-Year Cohort Study

por Tolomeo, Deborah, Orsucci, Daniele, Nesti, Claudia, Baldacci, Jacopo, Battini, Roberta, Bruno, Claudio, Bruno, Giorgia, Cassandrini, Denise, Doccini, Stefano, Donati, M. Alice, Ferrari, Annarita, Fiori, Simona, Fiorillo, Chiara, Guerrini, Renzo, Mari, Francesco, Montomoli, Martino, Pochiero, Francesca, Procopio, Elena, Ruggiero, Lucia, Sampaolo, Simone, Sicca, Federico, Ticci, Chiara, Rubegni, Anna, Santorelli, Filippo M.
Publicado 2021

SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy

por Vlaskamp, Danique R.M., Shaw, Benjamin J., Burgess, Rosemary, Mei, Davide, Montomoli, Martino, Xie, Han, Myers, Candace T., Bennett, Mark F., XiangWei, Wenshu, Williams, Danielle, Maas, Saskia M., Brooks, Alice S., Mancini, Grazia M.S., van de Laar, Ingrid M.B.H., van Hagen, Johanna M., Ware, Tyson L., Webster, Richard I., Malone, Stephen, Berkovic, Samuel F., Kalnins, Renate M., Sicca, Federico, Korenke, G. Christoph, van Ravenswaaij-Arts, Conny M.A., Hildebrand, Michael S., Mefford, Heather C., Jiang, Yuwu, Guerrini, Renzo, Scheffer, Ingrid E.
Publicado 2019