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European Journal of Medical Genetics|September 19, 2022
Abnormal course of the corticospinal tracts in KIF5C-related encephalopathyAlessandro Naim, Andrea Accogli, Elisabetta Amadori, et al.Frontiers in Pediatrics|May 14, 2023
Essential headaches in developmental age: What is changed before, during and after the lockdown for COVID-19 pandemic. Clinical studyAlice Bonuccelli, Greta Depietri, Tommaso Baldaccini, et al.BMC Medical Genomics|August 17, 2022
Expanding the genetic and clinical characteristics of Protocadherin 19 gene mutationsGiovanni Battista Dell'Isola, Elisabetta Mencaroni, Antonella Fattorusso, et al.Epilepsia|January 24, 2007
Lateralizing value of the auditory aura in partial seizuresIrene Florindo, Francesca Bisulli, Francesca Pittau, et al.Neuroradiology|October 9, 2015
Expanding the spectrum of congenital anomalies of the diencephalic-mesencephalic junctionMariasavina Severino, Domenico Tortora, Angela Pistorio, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 11, 2009
Heterogeneous seizure manifestations in Hypomelanosis of Ito: report of four new cases and review of the literatureKomi Assogba, Edoardo Ferlazzo, Pasquale Striano, et al.Frontiers in Pharmacology|December 28, 2020
A Volumetric Absorptive Microsampling Technique to Monitor Cannabidiol Levels in Epilepsy PatientsSara Dubois, Francesca Marchese, Federica Pigliasco, et al.Brain & Development|January 26, 2005
The movement disorders of Coffin-Lowry syndromeJohn B P Stephenson, Mary C Hoffman, Aline J C Russell, et al.Brain : a Journal of Neurology|January 17, 2022
Gene variant effects across sodium channelopathies predict function and guide precision therapyAndreas Brunklaus, Tony Feng, Tobias Brünger, et al.Journal of Medical Genetics|July 11, 2009
De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal originSarah E Heron, Ingrid E Scheffer, Xenia Iona, et al.Pageof 77