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Movement Disorders Clinical Practice|April 11, 2022
Neuroimaging Pearls from the MDS Congress Video Challenge. Part 1: Genetic DisordersDiana A Olszewska, Sapna Rawal, Conor Fearon, et al.Movement Disorders Clinical Practice|December 30, 2025
Racial and Ethnic Diversity in Clinical Trials for Disease Modifying Drugs in Parkinson Disease: A Systematic Review & Meta-AnalysisFarley Reis Rodrigues, Gabriel Bolner, Giovana Barros E Silva Ribeiro, et al.Epilepsia|June 3, 2022
MicroRNA inhibition using antimiRs in acute human brain tissue sectionsGareth Morris, Elena Langa, Conor Fearon, et al.Neurobiology of Aging|July 18, 2021
A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT geneDiana A Olszewska, Conor Fearon, Christopher McGuigan, et al.Movement Disorders Clinical Practice|July 20, 2024
Improving Parkinson's Disease Care through Systematic Screening for DepressionConnie Marras, Zachary Meyer, Hongliang Liu, et al.Movement Disorders Clinical Practice|April 11, 2022
Neuroimaging Pearls from the MDS Congress Video Challenge. Part 2: Acquired DisordersConor Fearon, Sapna Rawal, Diana Olszewska, et al.Journal of Neurology|March 21, 2023
COVID19-associated new-onset movement disorders: a follow-up studySusanne A Schneider, Soaham Desai, Onanong Phokaewvarangkul, et al.Arxiv|February 24, 2025
KMT2B-related disorders: expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulationLaura Cif, Diane Demailly, Jean-Pierre Lin, et al.Brain : a Journal of Neurology|November 5, 2020
KMT2B-related disorders: expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulationLaura Cif, Diane Demailly, Jean-Pierre Lin, et al.Pageof 6