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Parkinsonism & Related Disorders|June 22, 2013
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutationsChristina Sundal, Shinsuke Fujioka, Jay A Van Gerpen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 15, 2018
Multiple system atrophy and apolipoprotein EKotaro Ogaki, Yuka A Martens, Michael G Heckman, et al.
Parkinsonism & Related Disorders|July 5, 2016
MAPT haplotype diversity in multiple system atrophyCatherine Labbé, Michael G Heckman, Oswaldo Lorenzo-Betancor, et al.
American Journal of Human Genetics|March 16, 2007
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphismsStacey Melquist, David W Craig, Matthew J Huentelman, et al.
Parkinsonism & Related Disorders|July 24, 2021
Urine levels of the polyglutamine ataxin-3 protein are elevated in patients with spinocerebellar ataxia type 3Yuka Koike, Karen R Jansen-West, Rana Hanna Al-Shaikh, et al.
Neurology|November 8, 2014
LRRK2 exonic variants and risk of multiple system atrophyMichael G Heckman, Lucia Schottlaender, Alexandra I Soto-Ortolaza, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 2026
Longitudinal Dynamics of Polyglutamine-Expanded ATXN3 in Biofluids of Spinocerebellar Ataxia Type 3Jordan Bartfield, Lukasz Milanowski, Karen R Jansen-West, et al.
Neurology|June 10, 2009
Characterization of DCTN1 genetic variability in neurodegenerationC Vilariño-Güell, C Wider, A I Soto-Ortolaza, et al.
Acta Neuropathologica Communications|October 23, 2020
Association of ABI3 and PLCG2 missense variants with disease risk and neuropathology in Lewy body disease and progressive supranuclear palsySamantha L Strickland, Hélène Morel, Christian Prusinski, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|June 12, 2016
MAPT haplotype H1G is associated with increased risk of dementia with Lewy bodiesCatherine Labbé, Michael G Heckman, Oswaldo Lorenzo-Betancor, et al.
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