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Neurology|May 3, 2013
Similarities between familial and sporadic autopsy-proven progressive supranuclear palsyShinsuke Fujioka, Avi A Algom, Melissa E Murray, et al.
Human Mutation|May 6, 2015
Structural and Functional Impact of Parkinson Disease-Associated Mutations in the E3 Ubiquitin Ligase ParkinFabienne C Fiesel, Thomas R Caulfield, Elisabeth L Moussaud-Lamodière, et al.
Brain Communications|October 25, 2021
Evidence for GRN connecting multiple neurodegenerative diseasesMike A Nalls, Cornelis Blauwendraat, Lana Sargent, et al.
Brain : a Journal of Neurology|May 17, 2006
Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23Alexey Shatunov, Nyamkhishig Sambuughin, Joseph Jankovic, et al.
Neurobiology of Aging|November 27, 2012
Age-associated changes in gene expression in human brain and isolated neuronsAzad Kumar, J Raphael Gibbs, Alexandra Beilina, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 21, 2020
Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk ScoreHirotaka Iwaki, Cornelis Blauwendraat, Mary B Makarious, et al.
Orphanet Journal of Rare Diseases|November 4, 2017
Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegiaConceição Bettencourt, Vincenzo Salpietro, Stephanie Efthymiou, et al.
Acta Neuropathologica Communications|July 6, 2023
Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologiesShunsuke Koga, Aya Murakami, Alexandra I Soto-Beasley, et al.
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