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The Lancet. Neurology|August 2, 2011
Neuropathologically defined subtypes of Alzheimer's disease with distinct clinical characteristics: a retrospective studyMelissa E Murray, Neill R Graff-Radford, Owen A Ross, et al.Neurology International|January 14, 2014
Association of the APOE, MTHFR and ACE Genes Polymorphisms and Stroke in Zambian PatientsMasharip Atadzhanov, Mwila H Mwaba, Patrice N Mukomena, et al.Neuroscience Letters|June 16, 2009
DRD3 Ser9Gly and HS1BP3 Ala265Gly are not associated with Parkinson diseaseBrett H Keeling, Carles Vilariño-Güell, Owen A Ross, et al.Neurobiology of Disease|December 11, 2020
A population scale analysis of rare SNCA variation in the UK BiobankCornelis Blauwendraat, Mary B Makarious, Hampton L Leonard, et al.Circulation. Cardiovascular Genetics|February 5, 2011
The effect of survival bias on case-control genetic association studies of highly lethal diseasesChristopher D Anderson, Michael A Nalls, Alessandro Biffi, et al.Statistical Applications in Genetics and Molecular Biology|March 4, 2010
Comparing spatial maps of human population-genetic variation using Procrustes analysisChaolong Wang, Zachary A Szpiech, James H Degnan, et al.Neuroscience Letters|January 25, 2005
Unaltered alpha-synuclein blood levels in juvenile Parkinsonism with a parkin exon 4 deletionDavid W Miller, Anthony Crawley, Katrina Gwinn-Hardy, et al.Neurobiology of Aging|July 6, 2012
An exploratory analysis on gene-environment interactions for Parkinson diseaseJianjun Gao, Michael A Nalls, Min Shi, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|November 21, 2013
A Novel DYT-5 Mutation with Phenotypic Variability within a Colombian FamilyOscar Bernal-Pacheco, Genko Oyama, Angela Briton, et al.Mechanisms of Ageing and Development|August 10, 2005
LRRK2 mutations are not common in Alzheimer's diseaseMathias Toft, Sigrid Botne Sando, Stacey Melquist, et al.Pageof 76