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

Cynthia Crews

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
Journal of Women'S Health (2002)|August 31, 2004
Bulimia: medical complicationsPhilip S Mehler, Cynthia Crews, Kenneth Weiner
Alzheimer Disease and Associated Disorders|July 3, 2009
A case of dementia with PRNP D178Ncis-129M and no insomniaRita J Guerreiro, Tina Vaskov, Cynthia Crews, 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.
Journal of Renal Nutrition : the Official Journal of the Council on Renal Nutrition of the National Kidney Foundation|April 3, 2003
A survey of herbal product use in a dialysis population in Northwest OhioJames F Kleshinski, Cynthia Crews, Elisabeth Fry, 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.
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.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 8, 2017
Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern ItalyRosa Capozzo, Celeste Sassi, Monia B Hammer, et al.
The Lancet. Neurology|March 17, 2007
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of dataJennifer C Schymick, Sonja W Scholz, Hon-Chung Fung, et al.
Neuro-Degenerative Diseases|July 12, 2007
Comprehensive screening of a North American Parkinson's disease cohort for LRRK2 mutationJanel Johnson, Coro Paisán-Ruíz, Grisel Lopez, et al.
Neurogenetics|February 22, 2008
Structural genomic variation in ischemic strokeMar Matarin, Javier Simon-Sanchez, Hon-Chung Fung, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Women'S Health (2002)|August 31, 2004
Bulimia: medical complicationsPhilip S Mehler, Cynthia Crews, Kenneth Weiner
Alzheimer Disease and Associated Disorders|July 3, 2009
A case of dementia with PRNP D178Ncis-129M and no insomniaRita J Guerreiro, Tina Vaskov, Cynthia Crews, 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.
Journal of Renal Nutrition : the Official Journal of the Council on Renal Nutrition of the National Kidney Foundation|April 3, 2003
A survey of herbal product use in a dialysis population in Northwest OhioJames F Kleshinski, Cynthia Crews, Elisabeth Fry, 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.
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.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 8, 2017
Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern ItalyRosa Capozzo, Celeste Sassi, Monia B Hammer, et al.
The Lancet. Neurology|March 17, 2007
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of dataJennifer C Schymick, Sonja W Scholz, Hon-Chung Fung, et al.
Neuro-Degenerative Diseases|July 12, 2007
Comprehensive screening of a North American Parkinson's disease cohort for LRRK2 mutationJanel Johnson, Coro Paisán-Ruíz, Grisel Lopez, et al.
Neurogenetics|February 22, 2008
Structural genomic variation in ischemic strokeMar Matarin, Javier Simon-Sanchez, Hon-Chung Fung, et al.
Pageof 2