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Movement Disorders : Official Journal of the Movement Disorder Society|January 8, 2026
DBSMatchMaker: Global Uptake and Insights from the First Year of a Collaborative Deep Brain Stimulation PlatformJoshua Rong, Katerina Bernardi, Darius Ebrahimi-Fakhari, et al.
Current Opinion in Pediatrics|October 2, 2025
Early recognition of status dystonicus in children: a case-based approach for the general pediatricianAnn L Robbins, Kathryn Yang, Darius Ebrahimi-Fakhari, et al.
Movement Disorders Clinical Practice|October 22, 2024
Spectrum and Evolution of Movement Disorder Phenomenology in a Pediatric Powassan Encephalitis Case SeriesKathryn Yang, Rebecca Lindsay, Vicente Quiroz, et al.
Annals of Clinical and Translational Neurology|September 6, 2024
Juvenile-onset Huntington's disease - Spectrum and evolution of presenting movement disordersKathryn Yang, Vicente Quiroz, Amy Tam, et al.
Annals of Clinical and Translational Neurology|January 14, 2025
Blended phenotype of TECPR2-associated hereditary sensory-autonomic neuropathy and Temple syndromeUmar Zubair, Kathryn Yang, Luca Schierbaum, et al.
Annals of Clinical and Translational Neurology|January 27, 2025
Heterozygous variants in AP4S1 are not associated with a neurological phenotypeVicente Quiroz, Umar Zubair, Luca Schierbaum, et al.
Movement Disorders Clinical Practice|July 13, 2024
Autosomal Recessive Guanosine Triphosphate Cyclohydrolase I Deficiency: Redefining the Phenotypic Spectrum and OutcomesMaria Novelli, Manuela Tolve, Vicente Quiroz, et al.
Annals of Clinical and Translational Neurology|November 6, 2025
Health-Related Quality of Life in Rare Forms of Childhood-Onset Hereditary Spastic ParaplegiaHenri J D Schmidt, Nicole Battaglia, Joshua Rong, et al.
Annals of Clinical and Translational Neurology|April 25, 2026
Movement Disorders in Aicardi-Goutières Syndrome and Response to ImmunomodulationEnrique Gonzalez Saez-Diez, Monica Ferrer Socorro, Kathryn Yang, et al.
Movement Disorders Clinical Practice|May 29, 2025
Elevated Plasma Neurofilament Light Chain Levels in Children with Infantile-Onset Ascending Hereditary Spastic ParalysisUmar Zubair, Nicole Battaglia, Julian E Alecu, et al.
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