Showing results (31-40 of 37) with videos related to
Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Medrxiv : the Preprint Server for Health Sciences|January 31, 2024
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinaseEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.The Lancet. Neurology|April 13, 2024
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analysesEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.Communications Medicine|December 12, 2025
Clinical recognition of frontotemporal dementia with right temporal predominance: a consensus statement from the International Working GroupHulya Ulugut, Kyan Younes, Maxime Montembeault, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|July 10, 2024
Clinical recognition of frontotemporal dementia with right anterior temporal predominance: A multicenter retrospective cohort studyHulya Ulugut, Maxime Bertoux, Kyan Younes, et al.Movement Disorders Clinical Practice|July 23, 2026
Attitudes in Patients With Prodromal and Overt α-Synucleinopathy Toward Risk Disclosure: A Nationwide RegistryRezzak Yilmaz, Gülce Coşku Yılmaz Çakan, Yeşim Sücüllü Karadağ, et al.Medrxiv : the Preprint Server for Health Sciences|August 16, 2024
PSMF1 variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathwaysFrancesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.Nature Communications|April 15, 2026
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethalityFrancesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.Pageof 4