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 Zara

Showing results (81-90 of 398) with videos related to

Pageof 40
Sort By:
Epilepsia|April 6, 2011
The genetics of Dravet syndromeCarla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
International Journal of Molecular Sciences|June 24, 2022
Genomic Analysis Made It Possible to Identify Gene-Driver Alterations Covering the Time Window between Diagnosis of Neuroblastoma 4S and the Progression to Stage 4Marzia Ognibene, Patrizia De Marco, Stefano Parodi, et al.
Journal of Child Neurology|August 24, 2010
Genotype-phenotype correlations in a group of 15 SCN1A-mutated Italian patients with GEFS+ spectrum (seizures plus, classical and borderline severe myoclonic epilepsy of infancy)Francesco Nicita, Alberto Spalice, Laura Papetti, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 31, 2010
Familial nonkinesigenic paroxysmal dyskinesia and intracranial calcifications: a new syndrome?Nune S Yeghiazaryan, Pasquale Striano, Patrizia Accorsi, et al.
CNS Neuroscience & Therapeutics|November 11, 2024
Antisense oligonucleotides as a precision therapy for developmental and epileptic encephalopathiesPaloma García Quilón, Greta Volpedo, Serena Cappato, et al.
Acta Neurologica Belgica|December 1, 2010
A novel de novo SCN1A missense mutation in Severe Myoclonic Epilepsy BorderlandNicola Specchio, Marina Trivisano, Martina Balestri, et al.
Seizure|January 20, 2010
Galloway-Mowat syndrome: an early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literatureMarianna Pezzella, Nune S Yeghiazaryan, Pierangelo Veggiotti, et al.
Seizure|March 24, 2018
De novo 12q22.q23.3 duplication associated with temporal lobe epilepsyMaria Stella Vari, Monica Traverso, Tommaso Bellini, et al.
Archives of Neurology|February 14, 2007
Periodic myoclonus due to cytomegalovirus encephalitis in a patient with good syndromePasquale Striano, Fabio Tortora, Amelia Evoli, et al.
Seizure|April 25, 2018
Erratum to "De novo 12q22.q23.3 duplication associated with temporal lobe epilepsy" [Seizure 57 (2018) 63-65]Maria Stella Vari, Monica Traverso, Tommaso Bellini, et al.
Pageof 40

Showing results (81-90 of 398) with videos related to

Sort By:
Pageof 40
Epilepsia|April 6, 2011
The genetics of Dravet syndromeCarla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
International Journal of Molecular Sciences|June 24, 2022
Genomic Analysis Made It Possible to Identify Gene-Driver Alterations Covering the Time Window between Diagnosis of Neuroblastoma 4S and the Progression to Stage 4Marzia Ognibene, Patrizia De Marco, Stefano Parodi, et al.
Journal of Child Neurology|August 24, 2010
Genotype-phenotype correlations in a group of 15 SCN1A-mutated Italian patients with GEFS+ spectrum (seizures plus, classical and borderline severe myoclonic epilepsy of infancy)Francesco Nicita, Alberto Spalice, Laura Papetti, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 31, 2010
Familial nonkinesigenic paroxysmal dyskinesia and intracranial calcifications: a new syndrome?Nune S Yeghiazaryan, Pasquale Striano, Patrizia Accorsi, et al.
CNS Neuroscience & Therapeutics|November 11, 2024
Antisense oligonucleotides as a precision therapy for developmental and epileptic encephalopathiesPaloma García Quilón, Greta Volpedo, Serena Cappato, et al.
Acta Neurologica Belgica|December 1, 2010
A novel de novo SCN1A missense mutation in Severe Myoclonic Epilepsy BorderlandNicola Specchio, Marina Trivisano, Martina Balestri, et al.
Seizure|January 20, 2010
Galloway-Mowat syndrome: an early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literatureMarianna Pezzella, Nune S Yeghiazaryan, Pierangelo Veggiotti, et al.
Seizure|March 24, 2018
De novo 12q22.q23.3 duplication associated with temporal lobe epilepsyMaria Stella Vari, Monica Traverso, Tommaso Bellini, et al.
Archives of Neurology|February 14, 2007
Periodic myoclonus due to cytomegalovirus encephalitis in a patient with good syndromePasquale Striano, Fabio Tortora, Amelia Evoli, et al.
Seizure|April 25, 2018
Erratum to "De novo 12q22.q23.3 duplication associated with temporal lobe epilepsy" [Seizure 57 (2018) 63-65]Maria Stella Vari, Monica Traverso, Tommaso Bellini, et al.
Pageof 40