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Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|October 1, 2014
Epileptic encephalopathies: new genes and new pathwaysSahar Esmaeeli Nieh, Elliott H SherrCurrent Opinion in Pediatrics|November 25, 2003
The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypesElliott H SherrJournal of Neurogenetics|January 5, 2016
A de novo mutation in PRICKLE1 in fetal agenesis of the corpus callosum and polymicrogyriaAlexander G Bassuk, Elliott H SherrTrends in Molecular Medicine|July 8, 2023
The variant landscape and function of DDX3X in cancer and neurodevelopmental disordersMargaret Gadek, Elliott H Sherr, Stephen N FloorPediatric Neurology|April 16, 2008
Dilated perivascular spaces: an informative radiologic finding in Sanfilippo syndrome type ASimay Kara, Elliott H Sherr, A James BarkovichPlos Genetics|October 8, 2013
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyriaSamin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, et al.Annals of Clinical and Translational Neurology|July 1, 2015
De novo mutations in KIF1A cause progressive encephalopathy and brain atrophySahar Esmaeeli Nieh, Maura R Z Madou, Minhajuddin Sirajuddin, et al.Pediatric Neurology|April 18, 2022
De Novo GLI3 Pathogenic Variants May Cause Hypotonia and a Range of Brain Malformations Without Skeletal AbnormalitiesLyna Siafa, Emanuela Argilli, Elliott H Sherr, et al.American Journal of Medical Genetics. Part A|May 20, 2014
De novo ANKRD11 and KDM1A gene mutations in a male with features of KBG syndrome and Kabuki syndromeSanjin Tunovic, James Barkovich, Elliott H Sherr, et al.American Journal of Medical Genetics. Part A|July 22, 2008
Agenesis of the corpus callosum in California 1983-2003: a population-based studyHannah C Glass, Gary M Shaw, Chen Ma, et al.Pageof 12