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

J M Burgunder

Showing results (91-100 of 100) with videos related to

Pageof 10
Sort By:
You have reached the last page of results.This site can display upto 100 results.
European Journal of Neurology|March 20, 2010
EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementiasJ-M Burgunder, J Finsterer, Z Szolnoki, et al.
European Journal of Neurology|May 27, 2010
EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disordersJ-M Burgunder, L Schöls, J Baets, et al.
European Journal of Neurology|May 28, 2009
EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystoniasH F Harbo, J Finsterer, J Baets, et al.
European Journal of Neurology|January 7, 2010
EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegiasT Gasser, J Finsterer, J Baets, et al.
European Journal of Neurology|December 2, 2009
EFNS guidelines on the molecular diagnosis of mitochondrial disordersJ Finsterer, H F Harbo, J Baets, et al.
American Journal of Human Genetics|May 1, 1997
Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical originsI Richard, L Brenguier, P Dinçer, et al.
Human Molecular Genetics|March 4, 2000
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegiaN Fonknechten, D Mavel, P Byrne, et al.
Human Molecular Genetics|December 14, 2001
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1CM Brockington, Y Yuva, P Prandini, et al.
Neurobiology of Aging|March 31, 2009
Analysis of the UCHL1 genetic variant in Parkinson's disease among ChineseE K Tan, C S Lu, R Peng, et al.
European Journal of Neurology|January 30, 2014
Huntingtin gene CAG repeat numbers in Chinese patients with Huntington's disease and controlsH Jiang, Y M Sun, Y Hao, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
European Journal of Neurology|March 20, 2010
EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementiasJ-M Burgunder, J Finsterer, Z Szolnoki, et al.
European Journal of Neurology|May 27, 2010
EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disordersJ-M Burgunder, L Schöls, J Baets, et al.
European Journal of Neurology|May 28, 2009
EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystoniasH F Harbo, J Finsterer, J Baets, et al.
European Journal of Neurology|January 7, 2010
EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegiasT Gasser, J Finsterer, J Baets, et al.
European Journal of Neurology|December 2, 2009
EFNS guidelines on the molecular diagnosis of mitochondrial disordersJ Finsterer, H F Harbo, J Baets, et al.
American Journal of Human Genetics|May 1, 1997
Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical originsI Richard, L Brenguier, P Dinçer, et al.
Human Molecular Genetics|March 4, 2000
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegiaN Fonknechten, D Mavel, P Byrne, et al.
Human Molecular Genetics|December 14, 2001
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1CM Brockington, Y Yuva, P Prandini, et al.
Neurobiology of Aging|March 31, 2009
Analysis of the UCHL1 genetic variant in Parkinson's disease among ChineseE K Tan, C S Lu, R Peng, et al.
European Journal of Neurology|January 30, 2014
Huntingtin gene CAG repeat numbers in Chinese patients with Huntington's disease and controlsH Jiang, Y M Sun, Y Hao, et al.
Pageof 10