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

E Tournier-Lasserve

Showing results (41-50 of 100) with videos related to

Pageof 10
Sort By:
European Journal of Immunology|June 1, 1991
T cell response to myelin basic protein epitopes in multiple sclerosis patients and healthy subjectsR Liblau, E Tournier-Lasserve, J Maciazek, et al.
Journal of Neurology|November 10, 1998
Differential diagnosis of a vascular leukoencephalopathy within a CADASIL family: use of skin biopsy electron microscopy study and direct genotypic screeningA Furby, K Vahedi, M Force, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1988
Acute and regressive encephalopathy coincident with transient isolation of human immunodeficiency virus from cerebrospinal fluid of a seropositive manO Gout, B Rouquette, E Tournier-Lasserve, 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.
Clinical Genetics|November 21, 2013
Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformationsF Riant, S Odent, M Cecillon, et al.
Journal of Neurology|May 18, 2001
Sporadic late onset paroxysmal cerebellar ataxia in four unrelated patients: a new disease?J Julien, C Denier, X Ferrer, et al.
Cerebrovascular Diseases (Basel, Switzerland)|April 21, 1998
Cognitive alterations in non-demented CADASIL patientsH Taillia, H Chabriat, A Kurtz, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1995
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss familyH H Jung, C Bassetti, E Tournier-Lasserve, et al.
Translational Stroke Research|September 16, 2021
The Genetic Basis of Moyamoya DiseaseR Mertens, M Graupera, H Gerhardt, et al.
Revue Neurologique|September 16, 2019
Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature reviewO Osman, P Labrune, P Reiner, et al.
Pageof 10

Showing results (41-50 of 100) with videos related to

Sort By:
Pageof 10
European Journal of Immunology|June 1, 1991
T cell response to myelin basic protein epitopes in multiple sclerosis patients and healthy subjectsR Liblau, E Tournier-Lasserve, J Maciazek, et al.
Journal of Neurology|November 10, 1998
Differential diagnosis of a vascular leukoencephalopathy within a CADASIL family: use of skin biopsy electron microscopy study and direct genotypic screeningA Furby, K Vahedi, M Force, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1988
Acute and regressive encephalopathy coincident with transient isolation of human immunodeficiency virus from cerebrospinal fluid of a seropositive manO Gout, B Rouquette, E Tournier-Lasserve, 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.
Clinical Genetics|November 21, 2013
Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformationsF Riant, S Odent, M Cecillon, et al.
Journal of Neurology|May 18, 2001
Sporadic late onset paroxysmal cerebellar ataxia in four unrelated patients: a new disease?J Julien, C Denier, X Ferrer, et al.
Cerebrovascular Diseases (Basel, Switzerland)|April 21, 1998
Cognitive alterations in non-demented CADASIL patientsH Taillia, H Chabriat, A Kurtz, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1995
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss familyH H Jung, C Bassetti, E Tournier-Lasserve, et al.
Translational Stroke Research|September 16, 2021
The Genetic Basis of Moyamoya DiseaseR Mertens, M Graupera, H Gerhardt, et al.
Revue Neurologique|September 16, 2019
Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature reviewO Osman, P Labrune, P Reiner, et al.
Pageof 10