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American Journal of Human Genetics|August 20, 2025
Tackling a disease on a global scale, the Global Parkinson's Genetics Program, GP2: A new generation of opportunitiesCornelis Blauwendraat, Alastair J Noyce, Ignacio F Mata, et al.
Parkinson'S Disease|June 5, 2018
Sensitivity and Specificity of the ECAS in Parkinson's Disease and Progressive Supranuclear PalsyJennifer A Foley, Elaine H Niven, Andrew Paget, et al.
Human Molecular Genetics|January 15, 2021
Assessing the relationship between monoallelic PRKN mutations and Parkinson's riskSteven J Lubbe, Bernabe I Bustos, Jing Hu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 15, 2019
Proximity extension assay testing reveals novel diagnostic biomarkers of atypical parkinsonian syndromesEdwin Jabbari, John Woodside, Tong Guo, et al.
Journal of Neurology|October 31, 2012
The frequency of spinocerebellar ataxia type 23 in a UK populationKatherine Fawcett, Mohadeseh Mehrabian, Yo-Tsen Liu, et al.
Brain Communications|August 26, 2021
White matter abnormalities in active elite adult rugby playersKarl A Zimmerman, Etienne Laverse, Ravjeet Samra, et al.
Parkinsonism & Related Disorders|May 1, 2025
Diagnostic work up when suspecting early onset Parkinson disease (EOPD). Recommendations from the MDS EOPD study groupRaja Mehanna, Connie Marras, Jori Fleisher, et al.
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