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 P Bouchard

Showing results (71-80 of 96) with videos related to

Pageof 10
Sort By:
Electroencephalography and Clinical Neurophysiology. Supplement|January 1, 1990
Utility of short-latency evoked potentials in the classification of progressive, early onset cerebellar ataxiasM Vanasse, J Y Gabet, J De Léan, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy geneB Brais, J P Bouchard, F Gosselin, et al.
American Journal of Medical Genetics|September 6, 1996
Friedreich ataxia in Acadian families from eastern Canada: clinical diversity with conserved haplotypesA Richter, J Poirier, J Mercier, et al.
Neuropsychologia|September 2, 1998
Role of the striatum, cerebellum and frontal lobes in the automatization of a repeated visuomotor sequence of movementsJ Doyon, R Laforce, G Bouchard, et al.
Journal of Neuropathology and Experimental Neurology|September 28, 1999
Transplantation of human myoblasts in SCID mice as a potential muscular model for myotonic dystrophyD Skuk, D Furling, J P Bouchard, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Myoblast transplantation between monozygotic twin girl carriers of Duchenne muscular dystrophyJ P Tremblay, J P Bouchard, F Malouin, et al.
Brain : a Journal of Neurology|September 30, 2006
A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12J Jarry, M F Rioux, V Bolduc, et al.
Neurology|August 26, 2009
Cognitive impairment and reduced life span of oculopharyngeal muscular dystrophy homozygotesS C Blumen, J-P Bouchard, B Brais, et al.
Muscle & Nerve|May 1, 1992
Human myoblast transplantation: preliminary results of 4 casesJ Huard, J P Bouchard, R Roy, et al.
Human Molecular Genetics|March 1, 1995
The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13B Brais, Y G Xie, M Sanson, et al.
Pageof 10

Showing results (71-80 of 96) with videos related to

Sort By:
Pageof 10
Electroencephalography and Clinical Neurophysiology. Supplement|January 1, 1990
Utility of short-latency evoked potentials in the classification of progressive, early onset cerebellar ataxiasM Vanasse, J Y Gabet, J De Léan, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy geneB Brais, J P Bouchard, F Gosselin, et al.
American Journal of Medical Genetics|September 6, 1996
Friedreich ataxia in Acadian families from eastern Canada: clinical diversity with conserved haplotypesA Richter, J Poirier, J Mercier, et al.
Neuropsychologia|September 2, 1998
Role of the striatum, cerebellum and frontal lobes in the automatization of a repeated visuomotor sequence of movementsJ Doyon, R Laforce, G Bouchard, et al.
Journal of Neuropathology and Experimental Neurology|September 28, 1999
Transplantation of human myoblasts in SCID mice as a potential muscular model for myotonic dystrophyD Skuk, D Furling, J P Bouchard, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Myoblast transplantation between monozygotic twin girl carriers of Duchenne muscular dystrophyJ P Tremblay, J P Bouchard, F Malouin, et al.
Brain : a Journal of Neurology|September 30, 2006
A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12J Jarry, M F Rioux, V Bolduc, et al.
Neurology|August 26, 2009
Cognitive impairment and reduced life span of oculopharyngeal muscular dystrophy homozygotesS C Blumen, J-P Bouchard, B Brais, et al.
Muscle & Nerve|May 1, 1992
Human myoblast transplantation: preliminary results of 4 casesJ Huard, J P Bouchard, R Roy, et al.
Human Molecular Genetics|March 1, 1995
The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13B Brais, Y G Xie, M Sanson, et al.
Pageof 10