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Human Molecular Genetics|November 15, 2011
Mitochondrial autophagy in cells with mtDNA mutations results from synergistic loss of transmembrane potential and mTORC1 inhibitionRobert W Gilkerson, Rosa L A De Vries, Paul Lebot, et al.
Brain : a Journal of Neurology|November 19, 2024
Synaptic and cognitive impairment associated with L444P heterozygous glucocerebrosidase mutationWudu Lado, Ahrom Ham, Hongyu Li, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 27, 2004
Regulation of dopaminergic loss by Fas in a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's diseaseShawn Hayley, Stephen J Crocker, Patrice D Smith, et al.
Annals of Neurology|July 6, 2004
L-3-hydroxyacyl-CoA dehydrogenase II protects in a model of Parkinson's diseaseKim Tieu, Celine Perier, Miquel Vila, et al.
Annals of Neurology|September 27, 2014
Mendelian randomization of serum urate and parkinson disease progressionKelly Claire Simon, Shirley Eberly, Xiang Gao, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2021
Neuropathological Findings in a Case of Parkinsonism and Developmental Delay Associated with a Monoallelic Variant in PLXNA1Sarah A O'Shea, Richard A Hickman, Etty Cortes, et al.
The Journal of Clinical Investigation|January 17, 2018
Role for VGLUT2 in selective vulnerability of midbrain dopamine neuronsThomas Steinkellner, Vivien Zell, Zachary J Farino, et al.
Annals of Neurology|July 25, 2006
Proteasome inhibition and Parkinson's disease modelingJordi Bové, Chun Zhou, Vernice Jackson-Lewis, et al.
Parkinsonism & Related Disorders|September 24, 2013
Randomized trial of IPX066, carbidopa/levodopa extended release, in early Parkinson's diseaseRajesh Pahwa, Kelly E Lyons, Robert A Hauser, et al.
Movement Disorders Clinical Practice|May 22, 2018
Parkinson's Patients with Dyskinesia Switched from Immediate Release Amantadine to Open-label ADS-5102Stuart H Isaacson, Stanley Fahn, Rajesh Pahwa, et al.
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