Showing results (11-20 of 112) with videos related to

Sort By:
Pageof 12
Clinical Neurology and Neurosurgery|September 30, 2023
Frequency of SCN2A-related disorder in the regional epilepsy centre of brescia between 2002 and 2021Corinna Filippi, Giuseppe Milito, Patrizia Accorsi, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 29, 2006
Favorable outcome of cochlear implant in VIIIth nerve deficiencyDiego Zanetti, Maurizio Guida, Maria Grazia Barezzani, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 23, 2018
Expanding the phenotype of MED 17 mutations: Description of two new cases and review of the literatureAnnalisa Agostini, Daniela Marchetti, Claudia Izzi, et al.
Epilepsia|August 23, 2008
Two novel ALDH7A1 (antiquitin) splicing mutations associated with pyridoxine-dependent seizuresPasquale Striano, Silvia Battaglia, Lucio Giordano, et al.
Seizure|January 8, 2015
Do pure absence seizures occur in myoclonic epilepsy of infancy? A case seriesVincenzo Belcastro, Lucio Giordano, Dario Pruna, et al.
Epilepsy Research|August 23, 2017
Follow-up study of idiopathic generalized epilepsy with associated absence seizure and myoclonic epilepsy of infancyVincenzo Belcastro, Lucio Giordano, Dario Pruna, et al.
Journal of Medical Virology|January 14, 2005
Detection of herpesvirus-6A in a case of subacute cerebellitis and myoclonic dystoniaElisa Borghi, Elisabetta Pagani, Roberta Mancuso, et al.
The Journal of Bone and Joint Surgery. American Volume|November 4, 2009
Extracorporeal shock-wave therapy compared with surgery for hypertrophic long-bone nonunionsAngelo Cacchio, Lucio Giordano, Olivo Colafarina, et al.
Pageof 12