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

K Gwinn

Showing results (41-50 of 49) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 49 results.
Neurology|May 23, 2007
Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesiaM K Bruno, H-Y Lee, G W J Auburger, et al.
Nature Genetics|August 10, 2000
Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau proteinJ Lewis, E McGowan, J Rockwood, et al.
Clinical Genetics|February 6, 2004
Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's diseaseY R Wu, H Y Lin, C M Chen, et al.
European Neurology|July 27, 2004
DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patientsC K Wang, Y R Wu, W L Hwu, et al.
Science (New York, N.Y.)|November 1, 2003
alpha-Synuclein locus triplication causes Parkinson's diseaseA B Singleton, M Farrer, J Johnson, et al.
Epilepsia|October 9, 2002
ILAE genetics commission conference report: molecular analysis of complex genetic epilepsiesE Anderson, S Berkovic, O Dulac, et al.
Neurology|August 12, 2004
SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodiesJ Johnson, S M Hague, M Hanson, et al.
Neurology|January 26, 2005
The role of radiotracer imaging in Parkinson diseaseB Ravina, D Eidelberg, J E Ahlskog, et al.
Neurology|June 10, 2009
Characterization of DCTN1 genetic variability in neurodegenerationC Vilariño-Güell, C Wider, A I Soto-Ortolaza, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Neurology|May 23, 2007
Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesiaM K Bruno, H-Y Lee, G W J Auburger, et al.
Nature Genetics|August 10, 2000
Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau proteinJ Lewis, E McGowan, J Rockwood, et al.
Clinical Genetics|February 6, 2004
Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's diseaseY R Wu, H Y Lin, C M Chen, et al.
European Neurology|July 27, 2004
DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patientsC K Wang, Y R Wu, W L Hwu, et al.
Science (New York, N.Y.)|November 1, 2003
alpha-Synuclein locus triplication causes Parkinson's diseaseA B Singleton, M Farrer, J Johnson, et al.
Epilepsia|October 9, 2002
ILAE genetics commission conference report: molecular analysis of complex genetic epilepsiesE Anderson, S Berkovic, O Dulac, et al.
Neurology|August 12, 2004
SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodiesJ Johnson, S M Hague, M Hanson, et al.
Neurology|January 26, 2005
The role of radiotracer imaging in Parkinson diseaseB Ravina, D Eidelberg, J E Ahlskog, et al.
Neurology|June 10, 2009
Characterization of DCTN1 genetic variability in neurodegenerationC Vilariño-Güell, C Wider, A I Soto-Ortolaza, et al.
Pageof 5