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Neurology|January 25, 2022
Development and Validation of a Prediction Model for Early Diagnosis of SCN1A-Related EpilepsiesAndreas Brunklaus, Eduardo Pérez-Palma, Ismael Ghanty, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 18, 2021
Vaccination and childhood epilepsiesDana Craiu, Zvonka Rener Primec, Lieven Lagae, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|November 17, 2016
Positional plagiocephaly following ventriculoperitoneal shunting in neonates and infancy-how serious is it?Stuart A G Roberts, Joseph D Symonds, Reema Chawla, et al.
Journal of Medical Genetics|May 11, 2025
Novel biallelic NUP107 variants affect the nuclear pore complex and expand the clinical spectrum to include brain malformationsLoisa Dana Bonde, Laura Hecher, Malik Alawi, et al.
Epilepsy & Behavior : E&B|March 25, 2022
The clinical, economic, and humanistic burden of Dravet syndrome - A systematic literature reviewJoseph Sullivan, Alison M Deighton, Maria Candida Vila, 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.
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.
Neurology|July 22, 2020
Neuronal antibody prevalence in children with seizures under 3 years: A prospective national cohortJoseph D Symonds, Teresa C Moloney, Bethan Lang, et al.
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