Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Journal of Child Neurology|January 14, 2012
Changing child neurology training: evolution or revolution?Robert S Greenwood
Frontiers in Neurology|May 21, 2016
Stroke-Like Presentation Following Febrile Seizure in a Patient with 1q43q44 Deletion SyndromeJ Elliott Robinson, Stephanie M Wolfe, Kathleen Kaiser-Rogers, et al.
Health Affairs (Project Hope)|September 17, 2004
Did a rising tide lift all boats? The NIH budget and pediatric research portfolioDaniel P Gitterman, Robert S Greenwood, Keith C Kocis, et al.
Pediatric Neurology|March 19, 2002
Morphometric and neuropsychologic studies in children with arachnoid cystsMegdad M Zaatreh, Elizabeth R Bates, Stephen R Hooper, et al.
Archives of Neurology|December 14, 2005
Brain morphometry, T2-weighted hyperintensities, and IQ in children with neurofibromatosis type 1Robert S Greenwood, Larry A Tupler, J Kenneth Whitt, et al.
Neurology. Genetics|February 9, 2018
Diagnostic utility of exome sequencing in the evaluation of neuromuscular disordersGloria T Haskell, Michael C Adams, Zheng Fan, et al.
Journal of Inherited Metabolic Disease|February 13, 2019
Clinical, neuroradiological, and biochemical features of SLC35A2-CDG patientsMari-Anne Vals, Angel Ashikov, Pilvi Ilves, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 3, 2018
Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlationMagdalena Koczkowska, Tom Callens, Alicia Gomes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2018
Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlationMagdalena Koczkowska, Tom Callens, Alicia Gomes, et al.
Human Mutation|October 10, 2019
Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype-phenotype study in neurofibromatosis type 1Magdalena Koczkowska, Tom Callens, Yunjia Chen, et al.
Pageof 1