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

Lucia Fusco

Showing results (51-60 of 69) with videos related to

Pageof 7
Sort By:
Epilepsia|April 13, 2011
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutationsNicola Specchio, Carla Marini, Alessandra Terracciano, et al.
Neurogenetics|March 30, 2006
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the MediterraneanNatalia Cannelli, Denise Cassandrini, Enrico Bertini, et al.
Acta Neurologica Belgica|October 11, 2014
Acute intralesional recording in hypothalamic hamartoma: description of 4 casesNicola Specchio, Michele Rizzi, Marina Trivisano, et al.
Epilepsy & Behavior : E&B|November 30, 2006
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutationsPasquale Striano, Nicola Specchio, Roberta Biancheri, et al.
Epilepsy Research|November 17, 2009
Efficacy of levetiracetam in the treatment of drug-resistant Rett syndromeNicola Specchio, Martina Balestri, Pasquale Striano, et al.
Epilepsy Research|May 13, 2014
Hemispherotomy in Rasmussen encephalitis: long-term outcome in an Italian series of 16 patientsTiziana Granata, Sara Matricardi, Francesca Ragona, et al.
Epilepsia|November 14, 2019
Pediatric status epilepticus: Identification of prognostic factors using the new ILAE classification after 5 years of follow-upNicola Specchio, Nicola Pietrafusa, Marcello Bellusci, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 3, 2020
Posterior Reversible Encephalopathy Syndrome in infants and young childrenDuccio Maria Cordelli, Chiara Marra, Lara Ciampoli, et al.
International Journal of Molecular Sciences|July 13, 2024
A Case of CDKL5 Deficiency Due to an X Chromosome Pericentric Inversion: Delineation of Structural Rearrangements as an Overlooked Recurrent Pathological MechanismAntonietta Lombardo, Lorenzo Sinibaldi, Silvia Genovese, et al.
Human Mutation|February 26, 2019
Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathyDaniela Verrigni, Michela Di Nottia, Anna Ardissone, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
Epilepsia|April 13, 2011
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutationsNicola Specchio, Carla Marini, Alessandra Terracciano, et al.
Neurogenetics|March 30, 2006
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the MediterraneanNatalia Cannelli, Denise Cassandrini, Enrico Bertini, et al.
Acta Neurologica Belgica|October 11, 2014
Acute intralesional recording in hypothalamic hamartoma: description of 4 casesNicola Specchio, Michele Rizzi, Marina Trivisano, et al.
Epilepsy & Behavior : E&B|November 30, 2006
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutationsPasquale Striano, Nicola Specchio, Roberta Biancheri, et al.
Epilepsy Research|November 17, 2009
Efficacy of levetiracetam in the treatment of drug-resistant Rett syndromeNicola Specchio, Martina Balestri, Pasquale Striano, et al.
Epilepsy Research|May 13, 2014
Hemispherotomy in Rasmussen encephalitis: long-term outcome in an Italian series of 16 patientsTiziana Granata, Sara Matricardi, Francesca Ragona, et al.
Epilepsia|November 14, 2019
Pediatric status epilepticus: Identification of prognostic factors using the new ILAE classification after 5 years of follow-upNicola Specchio, Nicola Pietrafusa, Marcello Bellusci, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 3, 2020
Posterior Reversible Encephalopathy Syndrome in infants and young childrenDuccio Maria Cordelli, Chiara Marra, Lara Ciampoli, et al.
International Journal of Molecular Sciences|July 13, 2024
A Case of CDKL5 Deficiency Due to an X Chromosome Pericentric Inversion: Delineation of Structural Rearrangements as an Overlooked Recurrent Pathological MechanismAntonietta Lombardo, Lorenzo Sinibaldi, Silvia Genovese, et al.
Human Mutation|February 26, 2019
Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathyDaniela Verrigni, Michela Di Nottia, Anna Ardissone, et al.
Pageof 7