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Jose Bras

Showing results (21-30 of 118) with videos related to

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Movement Disorders Clinical Practice|October 9, 2020
Psychiatric Manifestations of <i>ATP13A2</i> MutationsBettina Balint, Joana Damasio, Francesca Magrinelli, et al.
F1000Research|September 21, 2017
Current concepts and controversies in the pathogenesis of Parkinson's disease dementia and Dementia with Lewy BodiesRimona S Weil, Tammaryn L Lashley, Jose Bras, et al.
Plos One|October 18, 2008
Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3Njideka Okubadejo, Angela Britton, Cynthia Crews, et al.
Neurobiology of Disease|May 23, 2020
Genetic architecture of common non-Alzheimer's disease dementiasRita Guerreiro, Elizabeth Gibbons, Miguel Tábuas-Pereira, et al.
Neurology. Genetics|June 9, 2016
Mutation of TBCK causes a rare recessive developmental disorderRita J Guerreiro, Rachel Brown, Donnai Dian, et al.
Acta Neurologica Scandinavica|March 21, 2022
Genetic analysis reveals novel variants for vascular cognitive impairmentSaana Mönkäre, Liina Kuuluvainen, Johanna Schleutker, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 27, 2022
In situ proximity labeling identifies Lewy pathology molecular interactions in the human brainBryan A Killinger, Lee L Marshall, Diptaman Chatterjee, et al.
Movement Disorders Clinical Practice|March 15, 2019
Action Myoclonus and Seizure in Kufor-Rakeb SyndromeMohammad Rohani, Anthony E Lang, Farzad Sina, et al.
Frontiers in Neurology|July 25, 2022
Exome Sequencing of a Portuguese Cohort of Frontotemporal Dementia Patients: Looking Into the ALS-FTD ContinuumMiguel Tábuas-Pereira, Isabel Santana, Elizabeth Gibbons, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|January 29, 2021
A Non-APOE Polygenic Risk Score for Alzheimer's Disease Is Associated With Cerebrospinal Fluid Neurofilament Light in a Representative Sample of Cognitively Unimpaired 70-Year OldsIngmar Skoog, Silke Kern, Jenna Najar, et al.
Pageof 12

Showing results (21-30 of 118) with videos related to

Sort By:
Pageof 12
Movement Disorders Clinical Practice|October 9, 2020
Psychiatric Manifestations of <i>ATP13A2</i> MutationsBettina Balint, Joana Damasio, Francesca Magrinelli, et al.
F1000Research|September 21, 2017
Current concepts and controversies in the pathogenesis of Parkinson's disease dementia and Dementia with Lewy BodiesRimona S Weil, Tammaryn L Lashley, Jose Bras, et al.
Plos One|October 18, 2008
Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3Njideka Okubadejo, Angela Britton, Cynthia Crews, et al.
Neurobiology of Disease|May 23, 2020
Genetic architecture of common non-Alzheimer's disease dementiasRita Guerreiro, Elizabeth Gibbons, Miguel Tábuas-Pereira, et al.
Neurology. Genetics|June 9, 2016
Mutation of TBCK causes a rare recessive developmental disorderRita J Guerreiro, Rachel Brown, Donnai Dian, et al.
Acta Neurologica Scandinavica|March 21, 2022
Genetic analysis reveals novel variants for vascular cognitive impairmentSaana Mönkäre, Liina Kuuluvainen, Johanna Schleutker, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 27, 2022
In situ proximity labeling identifies Lewy pathology molecular interactions in the human brainBryan A Killinger, Lee L Marshall, Diptaman Chatterjee, et al.
Movement Disorders Clinical Practice|March 15, 2019
Action Myoclonus and Seizure in Kufor-Rakeb SyndromeMohammad Rohani, Anthony E Lang, Farzad Sina, et al.
Frontiers in Neurology|July 25, 2022
Exome Sequencing of a Portuguese Cohort of Frontotemporal Dementia Patients: Looking Into the ALS-FTD ContinuumMiguel Tábuas-Pereira, Isabel Santana, Elizabeth Gibbons, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|January 29, 2021
A Non-APOE Polygenic Risk Score for Alzheimer's Disease Is Associated With Cerebrospinal Fluid Neurofilament Light in a Representative Sample of Cognitively Unimpaired 70-Year OldsIngmar Skoog, Silke Kern, Jenna Najar, et al.
Pageof 12