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Neuropediatrics|February 11, 2010
A syndrome with coarse face, mental retardation and unusual stereotyped movements*P Pavone, R R Trifiletti, E Parano, et al.Neuropediatrics|September 20, 2016
Neurologic Phenotypes Associated with Mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1, and IFIH1: Aicardi-Goutières Syndrome and BeyondJohn H Livingston, Yanick J CrowNeuropediatrics|May 9, 2017
Novel RRM2B Mutation and Severe Mitochondrial DNA Depletion: Report of 2 Cases and Review of the LiteratureNesia Kropach, Vered Shkalim-Zemer, Naama Orenstein, et al.Neuropediatrics|September 23, 2016
Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, TurkeyMehmet Canpolat, Hakan Gumus, Zubeyde Gunduz, et al.Neuropediatrics|April 10, 2018
Epileptic Encephalopathy in Adams-Oliver Syndrome Associated to a New DOCK6 Mutation: A Peculiar Behavioral PhenotypeLivia Pisciotta, Valeria Capra, Andrea Accogli, et al.Neuropediatrics|April 21, 2018
Surgical Treatment and Long-Term Outcome of Cerebral Cavernous Malformations-Related Epilepsy in Pediatric PatientsQiao Lin, Peng-Fan Yang, Yan-Zeng Jia, et al.Neuropediatrics|June 12, 2018
Management of Primary Tectal Plate Low-Grade Glioma in Pediatric Patients: Results of the Multicenter Treatment Study SIOP-LGG 2004Ariane Kaufmann, Nicolas U Gerber, Daniela Kandels, et al.Neuropediatrics|September 27, 2012
Validity of pediatric balance scales in children with spastic cerebral palsySook-Hee Yi, Ji Hye Hwang, Sang Jun Kim, et al.Neuropediatrics|November 1, 1981
The syndrome of absence of the septum pellucidum with porencephalies and other developmental defectsJ Aicardi, F GoutièresNeuropediatrics|November 1, 1981
A technique for evaluation of CSF shunt patency using telethermographyM Caldarelli, C Di Rocco, N Cellini, et al.Pageof 255