Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Federico Sicca

Showing results (31-40 of 47) with videos related to

Pageof 5
Sort By:
Annals of Clinical and Translational Neurology|April 3, 2020
Expanding the clinical and genetic heterogeneity of SPAX5Claudia Dosi, Daniele Galatolo, Anna Rubegni, et al.
Neurobiology of Disease|April 5, 2011
Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1Federico Sicca, Paola Imbrici, Maria Cristina D'Adamo, et al.
Plos One|March 11, 2016
Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant ZebrafishBrian P Grone, Maria Marchese, Kyla R Hamling, et al.
European Child & Adolescent Psychiatry|July 31, 2015
Temporal lobe connects regression and macrocephaly to autism spectrum disordersGiulia Valvo, Sara Baldini, Alessandra Retico, et al.
Epilepsia|April 13, 2011
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutationsNicola Specchio, Carla Marini, Alessandra Terracciano, et al.
International Journal of Molecular Sciences|June 24, 2022
Trehalose Treatment in Zebrafish Model of Lafora DiseaseStefania Della Vecchia, Asahi Ogi, Rosario Licitra, et al.
Plos One|October 3, 2013
Somatic overgrowth predisposes to seizures in autism spectrum disordersGiulia Valvo, Sara Baldini, Francesca Brachini, et al.
Epilepsia|June 15, 2007
Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalitiesCarla Marini, Davide Mei, Teresa Temudo, et al.
Neurology|February 17, 2017
Clinical and genetic factors predicting Dravet syndrome in infants with <i>SCN1A</i> mutationsValentina Cetica, Sara Chiari, Davide Mei, et al.
Scientific Reports|September 29, 2016
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsyFederico Sicca, Elena Ambrosini, Maria Marchese, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Annals of Clinical and Translational Neurology|April 3, 2020
Expanding the clinical and genetic heterogeneity of SPAX5Claudia Dosi, Daniele Galatolo, Anna Rubegni, et al.
Neurobiology of Disease|April 5, 2011
Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1Federico Sicca, Paola Imbrici, Maria Cristina D'Adamo, et al.
Plos One|March 11, 2016
Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant ZebrafishBrian P Grone, Maria Marchese, Kyla R Hamling, et al.
European Child & Adolescent Psychiatry|July 31, 2015
Temporal lobe connects regression and macrocephaly to autism spectrum disordersGiulia Valvo, Sara Baldini, Alessandra Retico, et al.
Epilepsia|April 13, 2011
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutationsNicola Specchio, Carla Marini, Alessandra Terracciano, et al.
International Journal of Molecular Sciences|June 24, 2022
Trehalose Treatment in Zebrafish Model of Lafora DiseaseStefania Della Vecchia, Asahi Ogi, Rosario Licitra, et al.
Plos One|October 3, 2013
Somatic overgrowth predisposes to seizures in autism spectrum disordersGiulia Valvo, Sara Baldini, Francesca Brachini, et al.
Epilepsia|June 15, 2007
Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalitiesCarla Marini, Davide Mei, Teresa Temudo, et al.
Neurology|February 17, 2017
Clinical and genetic factors predicting Dravet syndrome in infants with <i>SCN1A</i> mutationsValentina Cetica, Sara Chiari, Davide Mei, et al.
Scientific Reports|September 29, 2016
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsyFederico Sicca, Elena Ambrosini, Maria Marchese, et al.
Pageof 5