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Human Molecular Genetics|June 27, 2023
Classification of missense variants in the N-methyl-d-aspartate receptor GRIN gene family as gain- or loss-of-functionScott J Myers, Hongjie Yuan, Riley E Perszyk, et al.Cell Research|November 23, 2011
Direct reprogramming of human fibroblasts into dopaminergic neuron-like cellsXinjian Liu, Fang Li, Elizabeth A Stubblefield, et al.Genes|August 29, 2024
Clinical Features and Disease Progression in Older Individuals with Rett SyndromeJeffrey L Neul, Timothy A Benke, Eric D Marsh, et al.Annals of Neurology|May 9, 2024
Electroencephalographic Correlates of Clinical Severity in the Natural history study of RTT and Related DisordersJoni N Saby, Patrick J Mulcahey, Timothy A Benke, et al.The Journal of Pediatrics|December 22, 2009
Biomarkers of hypercoagulability and inflammation in childhood-onset arterial ischemic strokeTimothy J Bernard, Laura Z Fenton, Susan D Apkon, et al.Journal of Neurodevelopmental Disorders|March 4, 2023
Comparison of evoked potentials across four related developmental encephalopathiesJoni N Saby, Sarika U Peters, Timothy A Benke, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 12, 2018
The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2Jeffrey L Neul, Timothy A Benke, Eric D Marsh, et al.Annals of Neurology|January 22, 2021
Multisite Study of Evoked Potentials in Rett SyndromeJoni N Saby, Timothy A Benke, Sarika U Peters, et al.American Journal on Intellectual and Developmental Disabilities|November 19, 2020
A Psychometric Evaluation of the Motor-Behavioral Assessment Scale for Use as an Outcome Measure in Rett Syndrome Clinical TrialsMelissa Raspa, Carla M Bann, Angela Gwaltney, et al.Clinical Genetics|February 22, 2019
Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndromeSarika U Peters, Cary Fu, Bernhard Suter, et al.Pageof 5