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Andrew Singleton

Showing results (51-60 of 286) with videos related to

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Molecular Systems Biology|September 17, 2009
A simple and efficient algorithm for genome-wide homozygosity analysis in diseaseWei Liu, Jinhui Ding, Jesse Raphael Gibbs, 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.
Annals of Neurology|April 27, 2005
Torsin A haplotype predisposes to idiopathic dystoniaJordi Clarimon, Hilmir Asgeirsson, Andrew Singleton, et al.
Ageing Research Reviews|August 14, 2018
Shared biological pathways for frailty and cognitive impairment: A systematic reviewLana Sargent, Mike Nalls, Angela Starkweather, et al.
Journal of Neurology|December 14, 2004
Analysis of familial and sporadic restless legs syndrome in age of onset, gender, and severity featuresMelissa Hanson, Melissa Honour, Amanda Singleton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 27, 2005
Association of alpha-synuclein Rep1 polymorphism and Parkinson's disease: influence of Rep1 on age at onsetGeorgios M Hadjigeorgiou, Georgia Xiromerisiou, Vanessa Gourbali, et al.
The American Surgeon|April 24, 2024
Comparison and Utility of Intravenous Iodinated Contrast in Chest, Abdomen, Pelvis Computerized Tomography for Trauma Patients With Blunt Mechanism of Injury Before and After the May 9, 2022 Global Contrast Shortage at a Level II Trauma CenterJames Tran, Jasmine Park, Jade Nguyen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 3, 2006
Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's diseaseHon-Chung Fung, Chiung-Mei Chen, John Hardy, et al.
Plos One|June 12, 2008
TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosisRita J Guerreiro, Jennifer C Schymick, Cynthia Crews, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 27, 2005
Mutation of the Parkin gene in a Persian family: clinical progression over a 40-year periodJordi Clarimon, Janel Johnson, Ruth Djaldetti, et al.
Pageof 29

Showing results (51-60 of 286) with videos related to

Sort By:
Pageof 29
Molecular Systems Biology|September 17, 2009
A simple and efficient algorithm for genome-wide homozygosity analysis in diseaseWei Liu, Jinhui Ding, Jesse Raphael Gibbs, 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.
Annals of Neurology|April 27, 2005
Torsin A haplotype predisposes to idiopathic dystoniaJordi Clarimon, Hilmir Asgeirsson, Andrew Singleton, et al.
Ageing Research Reviews|August 14, 2018
Shared biological pathways for frailty and cognitive impairment: A systematic reviewLana Sargent, Mike Nalls, Angela Starkweather, et al.
Journal of Neurology|December 14, 2004
Analysis of familial and sporadic restless legs syndrome in age of onset, gender, and severity featuresMelissa Hanson, Melissa Honour, Amanda Singleton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 27, 2005
Association of alpha-synuclein Rep1 polymorphism and Parkinson's disease: influence of Rep1 on age at onsetGeorgios M Hadjigeorgiou, Georgia Xiromerisiou, Vanessa Gourbali, et al.
The American Surgeon|April 24, 2024
Comparison and Utility of Intravenous Iodinated Contrast in Chest, Abdomen, Pelvis Computerized Tomography for Trauma Patients With Blunt Mechanism of Injury Before and After the May 9, 2022 Global Contrast Shortage at a Level II Trauma CenterJames Tran, Jasmine Park, Jade Nguyen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 3, 2006
Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's diseaseHon-Chung Fung, Chiung-Mei Chen, John Hardy, et al.
Plos One|June 12, 2008
TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosisRita J Guerreiro, Jennifer C Schymick, Cynthia Crews, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 27, 2005
Mutation of the Parkin gene in a Persian family: clinical progression over a 40-year periodJordi Clarimon, Janel Johnson, Ruth Djaldetti, et al.
Pageof 29