Showing results (501-510 of 571) with videos related to
Sort By:
Pageof 58
Lancet (London, England)|July 4, 1998
Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative studyJ Burn, P Brennan, J Little, et al.Neurology|May 7, 2013
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson diseaseGavin Hudson, Mike Nalls, Jonathan R Evans, et al.Brain : a Journal of Neurology|July 16, 2015
Baseline and longitudinal grey matter changes in newly diagnosed Parkinson's disease: ICICLE-PD studyElijah Mak, Li Su, Guy B Williams, et al.Molecular Immunology|June 23, 2012
Factor H autoantibodies in membranoproliferative glomerulonephritisTimothy H J Goodship, Isabel Y Pappworth, Tibor Toth, et al.Scientific Reports|January 10, 2018
Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric refluxJohn M Darlow, Rebecca Darlay, Mark G Dobson, et al.Acta Neurologica Scandinavica|December 3, 2015
Olfaction in Parkin single and compound heterozygotes in a cohort of young onset Parkinson's disease patientsN Malek, D M A Swallow, K A Grosset, et al.Translational Psychiatry|February 3, 2016
Exome sequencing in dementia with Lewy bodiesM J Keogh, M Kurzawa-Akanbi, H Griffin, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 23, 2014
Cognitive impairment in multiple system atrophy: a position statement by the Neuropsychology Task Force of the MDS Multiple System Atrophy (MODIMSA) study groupIva Stankovic, Florian Krismer, Aleksandar Jesic, et al.Journal of the American Society of Nephrology : JASN|April 12, 2014
Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GNEdwin K S Wong, Holly E Anderson, Andrew P Herbert, et al.Nature Genetics|July 5, 2001
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseA R Curtis, C Fey, C M Morris, et al.Pageof 58