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Journal of Neurochemistry|September 14, 2017
Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathiesMaike F Dohrn, Nicola Glöckle, Lejla Mulahasanovic, et al.
Neurobiology of Aging|November 6, 2016
The dementia-associated APOE ε4 allele is not associated with rapid eye movement sleep behavior disorderZiv Gan-Or, Jacques Y Montplaisir, Jay P Ross, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 15, 2018
Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorderJiao Li, Jennifer A Ruskey, Isabelle Arnulf, et al.
Annals of Neurology|October 29, 2019
Genetic, Structural, and Functional Evidence Link TMEM175 to SynucleinopathiesLynne Krohn, Tuğba Nur Öztürk, Benoît Vanderperre, et al.
Plos One|June 26, 2023
The epidemiology of HIV population viral load in twelve sub-Saharan African countriesWolfgang Hladik, Paul Stupp, Stephen D McCracken, et al.
Neurology|November 4, 2020
The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on MMEJan Senderek, Petra Lassuthova, Dagmara Kabzińska, et al.
Annals of Neurology|January 25, 2020
Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt SynucleinopathiesLynne Krohn, Richard Y J Wu, Karl Heilbron, et al.
PNAS Nexus|August 28, 2025
Commonly observed sex differences in direct aggression are absent or reversed in sibling contextsMichael E W Varnum, Amanda P Kirsch, Daniel J Beal, et al.
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