Showing results (201-210 of 307) with videos related to
Sort By:
Pageof 31
Molecular Genetics & Genomic Medicine|May 18, 2018
Whole-exome sequencing for variant discovery in blepharospasmJun Tian, Satya R Vemula, Jianfeng Xiao, et al.Acta Neuropathologica|June 22, 2018
Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtypeShunsuke Koga, Naomi Kouri, Ronald L Walton, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 1999
Primary torsion dystonia: the search for genes is not overP R Jarman, N del Grosso, E M Valente, et al.American Journal of Neurodegenerative Disease|December 10, 2013
GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16Alexandra I Soto-Ortolaza, Michael G Heckman, Catherine Labbé, et al.Parkinsonism & Related Disorders|August 24, 2020
Screening non-MAPT genes of the Chr17q21 H1 haplotype in Parkinson's diseaseAlexandra I Soto-Beasley, Ronald L Walton, Rebecca R Valentino, et al.Parkinsonism & Related Disorders|February 13, 2018
Daytime sleepiness in dementia with Lewy bodies is associated with neuronal depletion of the nucleus basalis of MeynertKoji Kasanuki, Tanis J Ferman, Melissa E Murray, et al.JAMA Neurology|March 19, 2019
Association of MAPT Subhaplotypes With Risk of Progressive Supranuclear Palsy and Severity of Tau PathologyMichael G Heckman, Rebecca R Brennan, Catherine Labbé, et al.Parkinsonism & Related Disorders|January 2, 2007
Clinical-pathologic study of biomarkers in FTDP-17 (PPND family with N279K tau mutation)Zoe Arvanitakis, Robert J Witte, Dennis W Dickson, et al.Journal of Neuropathology and Experimental Neurology|February 7, 2007
Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutationsKeith A Josephs, Zeshan Ahmed, Omi Katsuse, et al.Parkinsonism & Related Disorders|October 23, 2012
Analysis of the C9orf72 repeat in Parkinson's disease, essential tremor and restless legs syndromeMariely Dejesus-Hernandez, Sruti Rayaprolu, Alexandra I Soto-Ortolaza, et al.Pageof 31