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Journal of the Neurological Sciences|September 7, 2021
Longitudinal risk factors for developing depressive symptoms in Parkinson's diseaseTarek Antar, Huw R Morris, Faraz Faghri, et al.
Neurobiology of Aging|October 5, 2014
Multiple system atrophy is not caused by C9orf72 hexanucleotide repeat expansionsSonja W Scholz, Elisa Majounie, Tamas Revesz, et al.
Neuroscience Letters|November 1, 2005
Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in TaiwanHon-Chung Fung, Chiung-Mei Chen, John Hardy, et al.
Plos One|August 23, 2012
Genome wide assessment of young onset Parkinson's disease from FinlandDena G Hernandez, Michael A Nalls, Pauli Ylikotila, et al.
Neurobiology of Aging|July 12, 2005
Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID)Parastoo Momeni, Nigel J Cairns, Robert H Perry, et al.
Neurobiology of Aging|May 30, 2015
EIF4G1 mutations do not cause Parkinson's diseaseNoah Nichols, Jose M Bras, Dena G Hernandez, et al.
Movement Disorders Clinical Practice|September 24, 2025
High Cerebrospinal DOPA Decarboxylase Level Predicts Cognitive Decline in Parkinson's DiseaseAndrea Sturchio, Wojciech Paslawski, Shervin Khosousi, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|January 31, 2025
Sex differences for regional pathology in people with a high likelihood of Lewy body dementia phenotype based on underlying pathologyEce Bayram, David G Coughlin, Shunsuke Koga, et al.
Parkinsonism & Related Disorders|March 19, 2024
Novel RAB39B loss-of-function mutation in patient with typical early-onset Parkinson's diseaseJessie R Jacobson, Capucine Piat, Allen J Aksamit, et al.
Frontiers in Neurology|July 9, 2020
Parkinson's Disease Research on the African Continent: Obstacles and OpportunitiesMarieke C J Dekker, Toumany Coulibaly, Soraya Bardien, et al.
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