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Annals of Neurology|September 15, 2010
Common mitochondrial sequence variants in ischemic strokeChristopher D Anderson, Alessandro Biffi, Rosanna Rahman, et al.
Parkinsonism & Related Disorders|January 15, 2015
TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter studySara Ortega-Cubero, Oswaldo Lorenzo-Betancor, Elena Lorenzo, et al.
Autophagy|December 5, 2022
Substitution of PINK1 Gly411 modulates substrate receptivity and turnoverFabienne C Fiesel, Dominika Fričová, Caleb S Hayes, et al.
Parkinsonism & Related Disorders|July 5, 2016
MAPT haplotype diversity in multiple system atrophyCatherine Labbé, Michael G Heckman, Oswaldo Lorenzo-Betancor, et al.
JAMA Neurology|July 25, 2018
Frequency of Loss of Function Variants in LRRK2 in Parkinson DiseaseCornelis Blauwendraat, Xylena Reed, Demis A Kia, et al.
Neuro-Oncology|December 6, 2022
Association of circulating markers with cognitive decline after radiation therapy for brain metastasisKristin Huntoon, S Keith Anderson, Karla V Ballman, et al.
Nature Communications|October 24, 2018
APOE ε2 is associated with increased tau pathology in primary tauopathyNa Zhao, Chia-Chen Liu, Alexandra J Van Ingelgom, et al.
Parkinsonism & Related Disorders|June 3, 2011
Lrrk2 p.Q1111H substitution and Parkinson's disease in Latin AmericaIgnacio F Mata, Greggory J Wilhoite, Dora Yearout, et al.
Neurology|November 8, 2014
LRRK2 exonic variants and risk of multiple system atrophyMichael G Heckman, Lucia Schottlaender, Alexandra I Soto-Ortolaza, et al.
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