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

David J Nicholl

Showing results (21-30 of 25) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 25 results.
Neurobiology of Aging|January 4, 2011
Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK seriesDaniel McNaughton, William Knight, Rita Guerreiro, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 5, 2014
Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosisVasyl Nesin, Graham Wiley, Maria Kousi, et al.
BMJ (Clinical Research Ed.)|November 18, 2010
Open letter to prime minister David Cameron and health secretary Andrew LansleyDavid J Nicholl, David Hilton-Jones, Jacqueline Palace, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2012
Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's diseaseLaura L Kilarski, Justin P Pearson, Victoria Newsway, et al.
The Lancet. Neurology|June 12, 2018
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing studyMarialuisa Quadri, Wim Mandemakers, Martyna M Grochowska, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Neurobiology of Aging|January 4, 2011
Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK seriesDaniel McNaughton, William Knight, Rita Guerreiro, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 5, 2014
Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosisVasyl Nesin, Graham Wiley, Maria Kousi, et al.
BMJ (Clinical Research Ed.)|November 18, 2010
Open letter to prime minister David Cameron and health secretary Andrew LansleyDavid J Nicholl, David Hilton-Jones, Jacqueline Palace, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2012
Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's diseaseLaura L Kilarski, Justin P Pearson, Victoria Newsway, et al.
The Lancet. Neurology|June 12, 2018
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing studyMarialuisa Quadri, Wim Mandemakers, Martyna M Grochowska, et al.
Pageof 3