Showing results (261-270 of 307) with videos related to

Sort By:
Pageof 31
Neurobiology of Aging|July 28, 2016
RAB39B gene mutations are not a common cause of Parkinson's disease or dementia with Lewy bodiesKyndall Hodges, Sheridan S Brewer, Catherine Labbé, et al.
Molecular Neurodegeneration|October 18, 2018
ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African AmericansOlivia J Conway, Minerva M Carrasquillo, Xue Wang, et al.
Neurology. Genetics|July 27, 2016
TREM2 p.R47H substitution is not associated with dementia with Lewy bodiesRonald L Walton, Alexandra I Soto-Ortolaza, Melissa E Murray, et al.
Parkinsonism & Related Disorders|May 10, 2005
The effect of tau genotype on clinical features in FTDP-17Yasuhiko Baba, Yoshio Tsuboi, Matthew C Baker, et al.
Neurology|March 14, 2008
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson diseaseK Haugarvoll, R Rademakers, J M Kachergus, et al.
Acta Neuropathologica Communications|July 14, 2022
Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measuresRebecca R Valentino, Chloe Ramnarine, Michael G Heckman, et al.
European Journal of Human Genetics : EJHG|December 8, 2005
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's diseaseAlessio Di Fonzo, Cristina Tassorelli, Michele De Mari, et al.
European Journal of Neurology|August 18, 2015
DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patientsO Lorenzo-Betancor, K Ogaki, A I Soto-Ortolaza, et al.
Neurology|November 13, 2015
Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disordersKotaro Ogaki, Shunsuke Koga, Michael G Heckman, et al.
Acta Neuropathologica|March 13, 2024
Role of GBA variants in Lewy body disease neuropathologyRonald L Walton, Shunsuke Koga, Alexandra I Beasley, et al.
Pageof 31