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Medrxiv : the Preprint Server for Health Sciences|October 31, 2023
Genome-wide association study identifies APOE and ZMIZ1 variants as mitophagy modifiers in Lewy body diseaseXu Hou, Michael G Heckman, Fabienne C Fiesel, et al.Journal of Neuropathology and Experimental Neurology|April 17, 2019
X-Linked Lymphoproliferative Syndrome Presenting as Adult-Onset Multi-Infarct DementiaPatrick R Blackburn, Wen-Lang Lin, David A Miller, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2009
GCH1 in early-onset Parkinson's diseaseStephanie A Cobb, Christian Wider, Owen A Ross, et al.Neurogenetics|April 7, 2010
LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.Parkinsonism & Related Disorders|October 26, 2010
Glucocerebrosidase mutations in diffuse Lewy body diseaseKenya Nishioka, Owen A Ross, Carles Vilariño-Güell, et al.BMC Medical Genetics|February 6, 2020
Targeted next-generation sequencing identifies novel variants in candidate genes for Parkinson's disease in Black South African and Nigerian patientsOluwafemi G Oluwole, Helena Kuivaniemi, Shameemah Abrahams, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 23, 2019
Ethnoracial differences in Alzheimer's disease from the FLorida Autopsied Multi-Ethnic (FLAME) cohortOctavio A Santos, Otto Pedraza, John A Lucas, et al.Neurology|November 11, 2018
PCNT point mutations and familial intracranial aneurysmsOswaldo Lorenzo-Betancor, Patrick R Blackburn, Emily Edwards, et al.Acta Neuropathologica|April 23, 2015
A novel tau mutation, p.K317N, causes globular glial tauopathyPawel Tacik, Michael DeTure, Wen-Lang Lin, et al.Molecular Neurodegeneration|March 11, 2014
ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's diseaseChristopher W Medway, Samer Abdul-Hay, Tynickwa Mims, et al.Pageof 50