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Showing results (81-90 of 86) with videos related to

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Neurology|October 27, 2004
Clinical and neuropathologic variation in neuronal intermediate filament inclusion diseaseN J Cairns, M Grossman, S E Arnold, et al.
Alzheimer Disease and Associated Disorders|September 13, 2019
Frequency of the TREM2 R47H Variant in Various Neurodegenerative DisordersAriane H Ayer, Kevin Wojta, Eliana Marisa Ramos, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 6, 2014
Tourette syndrome deep brain stimulation: a review and updated recommendationsLauren E Schrock, Jonathan W Mink, Douglas W Woods, et al.
Nature Communications|June 17, 2015
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsyNaomi Kouri, Owen A Ross, Beth Dombroski, et al.
Human Molecular Genetics|May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseasesGiovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
JAMA Neurology|March 26, 2014
A randomized clinical trial of high-dosage coenzyme Q10 in early Parkinson disease: no evidence of benefit, M Flint Beal, David Oakes, et al.
Pageof 9

Showing results (81-90 of 86) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 86 results.
Neurology|October 27, 2004
Clinical and neuropathologic variation in neuronal intermediate filament inclusion diseaseN J Cairns, M Grossman, S E Arnold, et al.
Alzheimer Disease and Associated Disorders|September 13, 2019
Frequency of the TREM2 R47H Variant in Various Neurodegenerative DisordersAriane H Ayer, Kevin Wojta, Eliana Marisa Ramos, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 6, 2014
Tourette syndrome deep brain stimulation: a review and updated recommendationsLauren E Schrock, Jonathan W Mink, Douglas W Woods, et al.
Nature Communications|June 17, 2015
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsyNaomi Kouri, Owen A Ross, Beth Dombroski, et al.
Human Molecular Genetics|May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseasesGiovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
JAMA Neurology|March 26, 2014
A randomized clinical trial of high-dosage coenzyme Q10 in early Parkinson disease: no evidence of benefit, M Flint Beal, David Oakes, et al.
Pageof 9