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NPJ Parkinson'S Disease|October 17, 2024
Parkinson's families project: a UK-wide study of early onset and familial Parkinson's diseaseClodagh Towns, Zih-Hua Fang, Manuela M X Tan, et al.
Annals of Neurology|July 29, 2025
Exenatide Once Weekly in the Treatment of Patients with Multiple System AtrophyNirosen Vijiaratnam, Christine Girges, Martin Wiegand, et al.
Human Molecular Genetics|November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceSteven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2012
Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's diseaseLaura L Kilarski, Justin P Pearson, Victoria Newsway, et al.
Brain : a Journal of Neurology|April 13, 2026
Data-driven modelling of tau pathology reveals distinct progressive supranuclear palsy subtypesPatrick W Cullinane, Jacy Bezerra Parmera, Hemanth Nelvagal, et al.
Human Molecular Genetics|August 16, 2012
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's diseaseMargaux F Keller, Mohamad Saad, Jose Bras, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
CNV-Finder: Streamlining Copy Number Variation DiscoveryNicole Kuznetsov, Kensuke Daida, Mary B Makarious, et al.
Human Molecular Genetics|December 11, 2012
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's diseasePeter Holmans, Valentina Moskvina, Lesley Jones, et al.
JAMA Neurology|June 7, 2017
Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune DiseasesAree Witoelar, Iris E Jansen, Yunpeng Wang, et al.
NPJ Parkinson'S Disease|April 2, 2022
Multi-modality machine learning predicting Parkinson's diseaseMary B Makarious, Hampton L Leonard, Dan Vitale, et al.
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