Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Haydeh Payami

Showing results (31-40 of 67) with videos related to

Pageof 7
Sort By:
Journal of Neurology, Neurosurgery, and Psychiatry|October 2, 2010
Postural instability/gait disturbance in Parkinson's disease has distinct subtypes: an exploratory analysisStewart A Factor, N Kyle Steenland, Donald S Higgins, et al.
American Journal of Human Genetics|July 13, 2004
Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2Ellen M Wijsman, E Warwick Daw, Change-En Yu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 27, 2005
Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinicsDenise M Kay, Cyrus P Zabetian, Stewart A Factor, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 25, 2018
Stool Immune Profiles Evince Gastrointestinal Inflammation in Parkinson's DiseaseMadelyn C Houser, Jianjun Chang, Stewart A Factor, et al.
American Journal of Human Genetics|November 5, 2013
Association of Parkinson disease with structural and regulatory variants in the HLA regionWilliam T Wissemann, Erin M Hill-Burns, Cyrus P Zabetian, et al.
Annals of Neurology|May 16, 2007
DBH -1021C-->T does not modify risk or age at onset in Parkinson's diseaseLani S Chun, Ali Samii, Carolyn M Hutter, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 3, 2003
SCA2 may present as levodopa-responsive parkinsonismHaydeh Payami, John Nutt, Steven Gancher, et al.
Annals of Neurology|December 26, 2006
Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patientsDenise M Kay, Dawn Moran, Lina Moses, et al.
Human Genetics|January 23, 2008
Exploring gene-environment interactions in Parkinson's diseaseColin C McCulloch, Denise M Kay, Stewart A Factor, et al.
Neurology. Genetics|April 29, 2016
DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficientLiyong Wang, Lizmarie Maldonado, Gary W Beecham, et al.
Pageof 7

Showing results (31-40 of 67) with videos related to

Sort By:
Pageof 7
Journal of Neurology, Neurosurgery, and Psychiatry|October 2, 2010
Postural instability/gait disturbance in Parkinson's disease has distinct subtypes: an exploratory analysisStewart A Factor, N Kyle Steenland, Donald S Higgins, et al.
American Journal of Human Genetics|July 13, 2004
Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2Ellen M Wijsman, E Warwick Daw, Change-En Yu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 27, 2005
Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinicsDenise M Kay, Cyrus P Zabetian, Stewart A Factor, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 25, 2018
Stool Immune Profiles Evince Gastrointestinal Inflammation in Parkinson's DiseaseMadelyn C Houser, Jianjun Chang, Stewart A Factor, et al.
American Journal of Human Genetics|November 5, 2013
Association of Parkinson disease with structural and regulatory variants in the HLA regionWilliam T Wissemann, Erin M Hill-Burns, Cyrus P Zabetian, et al.
Annals of Neurology|May 16, 2007
DBH -1021C-->T does not modify risk or age at onset in Parkinson's diseaseLani S Chun, Ali Samii, Carolyn M Hutter, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 3, 2003
SCA2 may present as levodopa-responsive parkinsonismHaydeh Payami, John Nutt, Steven Gancher, et al.
Annals of Neurology|December 26, 2006
Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patientsDenise M Kay, Dawn Moran, Lina Moses, et al.
Human Genetics|January 23, 2008
Exploring gene-environment interactions in Parkinson's diseaseColin C McCulloch, Denise M Kay, Stewart A Factor, et al.
Neurology. Genetics|April 29, 2016
DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficientLiyong Wang, Lizmarie Maldonado, Gary W Beecham, et al.
Pageof 7