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

Lewis P Rowland

Showing results (41-50 of 48) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 48 results.
Archives of Neurology|September 17, 2003
At jeopardy: the NIH as we know itRoger N Rosenberg, Timothy A Pedley, J Richard Baringer, et al.
Neurorehabilitation and Neural Repair|December 18, 2003
At jeopardy: the NIH as we know itRoger N Rosenberg, Timothy A Pedley, J Richard Baringer, et al.
Annals of Neurology|November 30, 2005
Prion protein codon 129 genotype prevalence is altered in primary progressive aphasiaXiaohong Li, Lewis P Rowland, Hiroshi Mitsumoto, et al.
Journal of the Neurological Sciences|March 4, 2008
A novel tRNA(Val) mitochondrial DNA mutation causing MELASKurenai Tanji, Petra Kaufmann, Ali B Naini, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 18, 2013
Peer recommendations on how to improve clinical research, and Conference wrap-upDavid A Chad, Lewis P Rowland, Carmel Armon, et al.
American Journal of Human Genetics|January 9, 2008
X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1Catarina M Quinzii, Tuan H Vu, K Christopher Min, et al.
Brain : a Journal of Neurology|August 23, 2015
Closing the tau loop: the missing tau mutationAllan McCarthy, Roisin Lonergan, Diana A Olszewska, et al.
Annals of Neurology|September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutationsNaomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Archives of Neurology|September 17, 2003
At jeopardy: the NIH as we know itRoger N Rosenberg, Timothy A Pedley, J Richard Baringer, et al.
Neurorehabilitation and Neural Repair|December 18, 2003
At jeopardy: the NIH as we know itRoger N Rosenberg, Timothy A Pedley, J Richard Baringer, et al.
Annals of Neurology|November 30, 2005
Prion protein codon 129 genotype prevalence is altered in primary progressive aphasiaXiaohong Li, Lewis P Rowland, Hiroshi Mitsumoto, et al.
Journal of the Neurological Sciences|March 4, 2008
A novel tRNA(Val) mitochondrial DNA mutation causing MELASKurenai Tanji, Petra Kaufmann, Ali B Naini, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 18, 2013
Peer recommendations on how to improve clinical research, and Conference wrap-upDavid A Chad, Lewis P Rowland, Carmel Armon, et al.
American Journal of Human Genetics|January 9, 2008
X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1Catarina M Quinzii, Tuan H Vu, K Christopher Min, et al.
Brain : a Journal of Neurology|August 23, 2015
Closing the tau loop: the missing tau mutationAllan McCarthy, Roisin Lonergan, Diana A Olszewska, et al.
Annals of Neurology|September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutationsNaomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Pageof 5