Showing results (11-20 of 29) with videos related to
Sort By:
Pageof 3
Parkinsonism & Related Disorders|April 17, 2025
Two case reports of RAB39B deletion displaying highly variable parkinsonismNicolas Geoffre, Paul Jaulent, Chloé Laurencin, et al.Journal of Neurology|November 20, 2012
MBNL1 gene variants as modifiers of disease severity in myotonic dystrophy type 1Vincent Huin, Francis Vasseur, Susanna Schraen-Maschke, et al.Neurology|September 11, 2015
A geographical cluster of progressive supranuclear palsy in northern FranceDominique Caparros-Lefebvre, Lawrence I Golbe, Vincent Deramecourt, et al.Parkinsonism & Related Disorders|September 27, 2017
Expanding the phenotype of SCA19/22: Parkinsonism, cognitive impairment and epilepsyVincent Huin, Isabelle Strubi-Vuillaume, Kathy Dujardin, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2016
The MAPT gene is differentially methylated in the progressive supranuclear palsy brainVincent Huin, Vincent Deramecourt, Dominique Caparros-Lefebvre, et al.Progress in Neurobiology|December 27, 2021
Neuronal ApoE4 stimulates C/EBPβ activation, promoting Alzheimer's disease pathology in a mouse modelZhi-Hao Wang, Yiyuan Xia, Zhourui Wu, et al.Ebiomedicine|April 15, 2025
HMGA1 deficiency: a pathogenic link between tau pathology and insulin resistanceMaria Mirabelli, Eusebio Chiefari, Biagio Arcidiacono, et al.Movement Disorders : Official Journal of the Movement Disorder Society|June 16, 2022
Functional Analyses of Two Novel LRRK2 Pathogenic Variants in Familial Parkinson's DiseaseIlda Coku, Eugénie Mutez, Sabiha Eddarkaoui, et al.Parkinsonism & Related Disorders|September 22, 2020
Isolated parkinsonism is an atypical presentation of GRN and C9orf72 gene mutationsFábio Carneiro, Dario Saracino, Vincent Huin, et al.Brain : a Journal of Neurology|December 20, 2019
Homozygous GRN mutations: new phenotypes and new insights into pathological and molecular mechanismsVincent Huin, Mathieu Barbier, Armand Bottani, et al.Pageof 3