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 (31-40 of 398) with videos related to

Pageof 40
Sort By:
Neurology|October 4, 2017
Teaching Neuro<i>Images</i>: Figure of 8: The clue to the diagnosis of AMPD2 pontocerebellar hypoplasia (PCH9)Mariasavina Severino, Federico Zara, Andrea Rossi, et al.
Brain : a Journal of Neurology|June 28, 2013
Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsyPasquale Striano, Federico Zara, Salvatore Striano, et al.
Seizure|April 1, 2019
Familial adult myoclonic epilepsy: A new expansion repeats disorderIlaria Lagorio, Federico Zara, Salvatore Striano, et al.
Current Research in Translational Medicine|March 17, 2024
Validation of analytical methods for the production of expanded γδ T lymphocytes useful for therapeutic purposesFabio Morandi, Martina Della Lastra, Federico Zara, et al.
Journal of the Neurological Sciences|July 8, 2008
Topiramate-associated worsening symptoms in a patient with familial hemiplegic migrainePasquale Striano, Federico Zara, Filippo Maria Santorelli, et al.
Epilepsia|May 28, 2009
Familial benign nonprogressive myoclonic epilepsiesPasquale Striano, Fabrizio A de Falco, Carlo Minetti, et al.
Archives of Neurology|May 11, 2011
Hemidystonia in uncontrolled type 2 diabetes mellitusPasquale Striano, Ferdinando Caranci, Sabina Pappatà, et al.
Epilepsy Research|March 24, 2009
Addition of verapamil in the treatment of severe myoclonic epilepsy in infancyPaola Iannetti, Pasquale Parisi, Alberto Spalice, et al.
European Journal of Human Genetics : EJHG|July 6, 2012
Do regulatory regions matter in FOXG1 duplications?Antonio Falace, Nicola Vanni, Antonello Mallamaci, et al.
Pediatric Blood & Cancer|June 28, 2024
Overexpression of H2AFX gene in neuroblastoma is associated with worse prognosisMarzia Ognibene, Stefano Parodi, Loredana Amoroso, et al.
Pageof 40

Showing results (31-40 of 398) with videos related to

Sort By:
Pageof 40
Neurology|October 4, 2017
Teaching Neuro<i>Images</i>: Figure of 8: The clue to the diagnosis of AMPD2 pontocerebellar hypoplasia (PCH9)Mariasavina Severino, Federico Zara, Andrea Rossi, et al.
Brain : a Journal of Neurology|June 28, 2013
Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsyPasquale Striano, Federico Zara, Salvatore Striano, et al.
Seizure|April 1, 2019
Familial adult myoclonic epilepsy: A new expansion repeats disorderIlaria Lagorio, Federico Zara, Salvatore Striano, et al.
Current Research in Translational Medicine|March 17, 2024
Validation of analytical methods for the production of expanded γδ T lymphocytes useful for therapeutic purposesFabio Morandi, Martina Della Lastra, Federico Zara, et al.
Journal of the Neurological Sciences|July 8, 2008
Topiramate-associated worsening symptoms in a patient with familial hemiplegic migrainePasquale Striano, Federico Zara, Filippo Maria Santorelli, et al.
Epilepsia|May 28, 2009
Familial benign nonprogressive myoclonic epilepsiesPasquale Striano, Fabrizio A de Falco, Carlo Minetti, et al.
Archives of Neurology|May 11, 2011
Hemidystonia in uncontrolled type 2 diabetes mellitusPasquale Striano, Ferdinando Caranci, Sabina Pappatà, et al.
Epilepsy Research|March 24, 2009
Addition of verapamil in the treatment of severe myoclonic epilepsy in infancyPaola Iannetti, Pasquale Parisi, Alberto Spalice, et al.
European Journal of Human Genetics : EJHG|July 6, 2012
Do regulatory regions matter in FOXG1 duplications?Antonio Falace, Nicola Vanni, Antonello Mallamaci, et al.
Pediatric Blood & Cancer|June 28, 2024
Overexpression of H2AFX gene in neuroblastoma is associated with worse prognosisMarzia Ognibene, Stefano Parodi, Loredana Amoroso, et al.
Pageof 40