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

M Pandolfo

Showing results (111-120 of 116) with videos related to

Pageof 12
Sort By:
You have reached the last page of results.This site can display upto 116 results.
Annals of Neurology|February 16, 1999
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotesM Cossée, A Dürr, M Schmitt, et al.
Neurology|June 14, 2006
Scale for the assessment and rating of ataxia: development of a new clinical scaleT Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, et al.
Archives of Neurology|April 10, 2002
Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locusI Silveira, C Miranda, L Guimarães, et al.
Science (New York, N.Y.)|March 8, 1996
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansionV Campuzano, L Montermini, M D Moltò, et al.
Neurology|August 8, 2008
Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptomsT Schmitz-Hübsch, M Coudert, P Bauer, et al.
Neurology|August 12, 2011
The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up studyH Jacobi, P Bauer, P Giunti, et al.
Pageof 12

Showing results (111-120 of 116) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 116 results.
Annals of Neurology|February 16, 1999
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotesM Cossée, A Dürr, M Schmitt, et al.
Neurology|June 14, 2006
Scale for the assessment and rating of ataxia: development of a new clinical scaleT Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, et al.
Archives of Neurology|April 10, 2002
Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locusI Silveira, C Miranda, L Guimarães, et al.
Science (New York, N.Y.)|March 8, 1996
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansionV Campuzano, L Montermini, M D Moltò, et al.
Neurology|August 8, 2008
Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptomsT Schmitz-Hübsch, M Coudert, P Bauer, et al.
Neurology|August 12, 2011
The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up studyH Jacobi, P Bauer, P Giunti, et al.
Pageof 12