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Neurology. Genetics|September 9, 2016
Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48)Jennifer Hirst, Marianna Madeo, Katrien Smets, et al.Neurology. Genetics|September 21, 2016
GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysisVictoria Mallett, Jay P Ross, Roy N Alcalay, et al.Neurology. Genetics|September 8, 2016
KCNQ2 encephalopathy: Features, mutational hot spots, and ezogabine treatment of 11 patientsJohn J Millichap, Kristen L Park, Tammy Tsuchida, et al.Neurology. Genetics|May 17, 2017
Intragenic DOK7 deletion detected by whole-genome sequencing in congenital myasthenic syndromesYoshiteru Azuma, Ana Töpf, Teresinha Evangelista, et al.Neurology. Genetics|June 30, 2017
Abnormal expression of homeobox genes and transthyretin in C9ORF72 expansion carriersNiCole A Finch, Xue Wang, Matthew C Baker, et al.Neurology. Genetics|August 15, 2022
A Remote Longitudinal Observational Study of Individuals at Genetic Risk for Parkinson Disease: Baseline ResultsStella Jensen-Roberts, Taylor L Myers, Peggy Auinger, et al.Neurology. Genetics|September 10, 2021
Dysfunctional Homozygous VRK1-D263G Variant Impairs the Assembly of Cajal Bodies and DNA Damage Response in Hereditary Spastic ParaplegiaPatricia Morejon-Garcia, Boris Keren, Iñigo Marcos-Alcalde, et al.Neurology. Genetics|December 8, 2025
Deciphering Spastic Ataxia: Clinical and Genetic ProfilesJoana Damásio, Mariana Santos, Sara Costa, et al.Neurology. Genetics|December 26, 2025
Pediatric Cohort of Charcot-Marie-Tooth Disease: Clinical Features and Genetic DistributionIssa Alawneh, Alberto Alemán, Elisa Nigro, et al.Pageof 86