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

P Labauge

Showing results (71-80 of 142) with videos related to

Pageof 15
Sort By:
Neurology|October 24, 2001
The prevalence of Sjögren syndrome in patients with primary progressive multiple sclerosisJ de Seze, D Devos, G Castelnovo, et al.
Cerebrovascular Diseases (Basel, Switzerland)|April 19, 2013
Isolated lacunar infarct: an early clinical presentation of CADASIL?C Carra-Dallière, X Ayrignac, D Renard, et al.
Annals of Neurology|February 16, 1999
An association between autosomal dominant cerebral cavernomas and a distinctive hyperkeratotic cutaneous vascular malformation in 4 familiesP Labauge, O Enjolras, J J Bonerandi, et al.
Revue Neurologique|April 29, 2008
[A retrospective study of six patients with late-onset Pompe disease]A Saux, P Laforet, A M Pagès, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1997
[Regressive pseudobulbar syndrome associated with acute viral hepatitis B]J F Bourgaux, M Herpe, J Barki, et al.
European Journal of Neurology|January 5, 2016
Brain magnetic resonance imaging helps to differentiate atypical multiple sclerosis with cavitary lesions and vanishing white matter diseaseX Ayrignac, N Menjot de Champfleur, S Menjot de Champfleur, et al.
Revue Neurologique|July 21, 2009
Familial cortical myoclonic tremor with epilepsy (FCMTE): Clinical characteristics and exclusion of linkages to 8q and 2p in a large French familyE Magnin, M Vidailhet, C Depienne, et al.
Journal of Neurology|May 11, 2016
Two cases of relapses in primary progressive multiple sclerosis after fingolimod withdrawalJean-Baptiste Davion, M Cambron, E Duhin, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST (SPG4). Disease: Spastic paraparesis. Accession #Hm0552C Depienne, C Tallaksen, J Y Lephay, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0553C Depienne, C Tallaksen, J Y Lephay, et al.
Pageof 15

Showing results (71-80 of 142) with videos related to

Sort By:
Pageof 15
Neurology|October 24, 2001
The prevalence of Sjögren syndrome in patients with primary progressive multiple sclerosisJ de Seze, D Devos, G Castelnovo, et al.
Cerebrovascular Diseases (Basel, Switzerland)|April 19, 2013
Isolated lacunar infarct: an early clinical presentation of CADASIL?C Carra-Dallière, X Ayrignac, D Renard, et al.
Annals of Neurology|February 16, 1999
An association between autosomal dominant cerebral cavernomas and a distinctive hyperkeratotic cutaneous vascular malformation in 4 familiesP Labauge, O Enjolras, J J Bonerandi, et al.
Revue Neurologique|April 29, 2008
[A retrospective study of six patients with late-onset Pompe disease]A Saux, P Laforet, A M Pagès, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1997
[Regressive pseudobulbar syndrome associated with acute viral hepatitis B]J F Bourgaux, M Herpe, J Barki, et al.
European Journal of Neurology|January 5, 2016
Brain magnetic resonance imaging helps to differentiate atypical multiple sclerosis with cavitary lesions and vanishing white matter diseaseX Ayrignac, N Menjot de Champfleur, S Menjot de Champfleur, et al.
Revue Neurologique|July 21, 2009
Familial cortical myoclonic tremor with epilepsy (FCMTE): Clinical characteristics and exclusion of linkages to 8q and 2p in a large French familyE Magnin, M Vidailhet, C Depienne, et al.
Journal of Neurology|May 11, 2016
Two cases of relapses in primary progressive multiple sclerosis after fingolimod withdrawalJean-Baptiste Davion, M Cambron, E Duhin, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST (SPG4). Disease: Spastic paraparesis. Accession #Hm0552C Depienne, C Tallaksen, J Y Lephay, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0553C Depienne, C Tallaksen, J Y Lephay, et al.
Pageof 15