Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Movement Disorders : Official Journal of the Movement Disorder Society|September 4, 2020
A Phase 1 Randomized Trial of Specific Active α-Synuclein Immunotherapies PD01A and PD03A in Multiple System AtrophyWassilios G Meissner, Anne Pavy-Le Traon, Alexandra Foubert-Samier, et al.
Movement Disorders Clinical Practice|July 7, 2020
The Prevalence and Determinants of Neuropsychiatric Symptoms in Late-Stage ParkinsonismAdrianus L A J Hommel, Marjan J Meinders, Stefan Lorenzl, et al.
Neurology|January 8, 2017
Characteristics in limbic encephalitis with anti-adenylate kinase 5 autoantibodiesLe-Duy Do, Eve Chanson, Virginie Desestret, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 2024
Care of Late-Stage Parkinsonism: Resource Utilization of the Disease in Five European CountriesChristopher Kruse, Anna Lipinski, Malte Verheyen, et al.
The New England Journal of Medicine|April 10, 2024
Trial of Lixisenatide in Early Parkinson's DiseaseWassilios G Meissner, Philippe Remy, Caroline Giordana, et al.
European Journal of Neurology|June 28, 2025
Neuropathy in GAA-FGF14 Late-Onset Cerebellar Ataxia (SCA27B): Prevalence and CharacteristicsJulian Theuriet, Lukas Paulet, Blandine Acket, et al.
Brain : a Journal of Neurology|July 29, 2022
Neurofilament light levels predict clinical progression and death in multiple system atrophyViorica Chelban, Elham Nikram, Alexandra Perez-Soriano, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2021
High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 familiesMehdi Benkirane, Cecilia Marelli, Claire Guissart, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 28, 2024
Assessment of Mendelian and risk-factor genes in Alzheimer disease: A prospective nationwide clinical utility study and recommendations for genetic screeningGaël Nicolas, Aline Zaréa, Morgane Lacour, et al.
Pageof 2