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B Singleton

Showing results (141-150 of 477) with videos related to

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JAMA Neurology|July 16, 2014
Genome-wide analysis of the heritability of amyotrophic lateral sclerosisMargaux F Keller, Luigi Ferrucci, Andrew B Singleton, et al.
British Journal of Pharmacology|October 8, 1999
Inhibition of the human ether-a-go-go-related gene (HERG) potassium channel by cisapride: affinity for open and inactivated statesB D Walker, C B Singleton, J A Bursill, et al.
Arthroscopy : the Journal of Arthroscopic & Related Surgery : Official Publication of the Arthroscopy Association of North America and the International Arthroscopy Association|November 2, 2010
A comparison of forearm supination and elbow flexion strength in patients with long head of the biceps tenotomy or tenodesisJohn R Shank, Steven B Singleton, Sepp Braun, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2006
Assessing the role of DRD5 and DYT1 in two different case-control series with primary blepharospasmJordi Clarimon, Francesco Brancati, Elizabeth Peckham, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Case-control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's diseaseJohn L Goudreau, Demetrius M Maraganore, Matthew J Farrer, et al.
Annals of Neurology|November 15, 2001
Case-Control study of the extended tau gene haplotype in Parkinson's diseaseD M Maraganore, D G Hernandez, A B Singleton, et al.
Neurobiology of Disease|August 9, 2005
Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosisMichael L Garcia, Andrew B Singleton, Dena Hernandez, et al.
Journal of Alzheimer'S Disease : JAD|June 4, 2016
A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern ItalyCeleste Sassi, Rosa Capozzo, Raphael Gibbs, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 20, 2021
Coding and Noncoding Variation in LRRK2 and Parkinson's Disease RiskJulie Lake, Xylena Reed, Rebekah G Langston, et al.
Medrxiv : the Preprint Server for Health Sciences|July 29, 2024
Association of CSF α-Synuclein Seed Amplification Assay Positivity with Disease Progression and Cognitive Decline: A Longitudinal Alzheimer's Disease Neuroimaging Initiative StudyDuygu Tosun, Zachary Hausle, Pamela Thropp, et al.
Pageof 48

Showing results (141-150 of 477) with videos related to

Sort By:
Pageof 48
JAMA Neurology|July 16, 2014
Genome-wide analysis of the heritability of amyotrophic lateral sclerosisMargaux F Keller, Luigi Ferrucci, Andrew B Singleton, et al.
British Journal of Pharmacology|October 8, 1999
Inhibition of the human ether-a-go-go-related gene (HERG) potassium channel by cisapride: affinity for open and inactivated statesB D Walker, C B Singleton, J A Bursill, et al.
Arthroscopy : the Journal of Arthroscopic & Related Surgery : Official Publication of the Arthroscopy Association of North America and the International Arthroscopy Association|November 2, 2010
A comparison of forearm supination and elbow flexion strength in patients with long head of the biceps tenotomy or tenodesisJohn R Shank, Steven B Singleton, Sepp Braun, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2006
Assessing the role of DRD5 and DYT1 in two different case-control series with primary blepharospasmJordi Clarimon, Francesco Brancati, Elizabeth Peckham, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Case-control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's diseaseJohn L Goudreau, Demetrius M Maraganore, Matthew J Farrer, et al.
Annals of Neurology|November 15, 2001
Case-Control study of the extended tau gene haplotype in Parkinson's diseaseD M Maraganore, D G Hernandez, A B Singleton, et al.
Neurobiology of Disease|August 9, 2005
Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosisMichael L Garcia, Andrew B Singleton, Dena Hernandez, et al.
Journal of Alzheimer'S Disease : JAD|June 4, 2016
A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern ItalyCeleste Sassi, Rosa Capozzo, Raphael Gibbs, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 20, 2021
Coding and Noncoding Variation in LRRK2 and Parkinson's Disease RiskJulie Lake, Xylena Reed, Rebekah G Langston, et al.
Medrxiv : the Preprint Server for Health Sciences|July 29, 2024
Association of CSF α-Synuclein Seed Amplification Assay Positivity with Disease Progression and Cognitive Decline: A Longitudinal Alzheimer's Disease Neuroimaging Initiative StudyDuygu Tosun, Zachary Hausle, Pamela Thropp, et al.
Pageof 48