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E Tournier-Lasserve

Showing results (61-70 of 100) with videos related to

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Genomics|December 1, 1996
A human homolog of bacterial acetolactate synthase genes maps within the CADASIL critical regionA Joutel, A Ducros, S Alamowitch, et al.
Stroke|February 5, 1999
Brain stem MRI signal abnormalities in CADASILH Chabriat, R Mrissa, C Levy, et al.
Bulletin De L'Academie Nationale De Medecine|March 23, 2001
[CADASIL: genetics and physiopathology]A Joutel, A François, H Chabriat, et al.
Archives of Neurology|March 1, 1989
Chronic myelopathies associated with human T-lymphotropic virus type I. A clinical, serologic, and immunovirologic study of ten patients in FranceO Gout, A Gessain, F Bolgert, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 4, 2011
[Genetic syndromes that mimic congenital infections: report of 2 cases]M Thibault, J Leydet, E Tournier-Lasserve, et al.
The New England Journal of Medicine|July 7, 2001
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channelA Ducros, C Denier, A Joutel, et al.
Revue Neurologique|October 14, 2018
A novel large deletion in CCM1 gene in a Tunisian familyF Tinsa, I Bel Hadj, F Riant, et al.
Revue Neurologique|January 1, 1986
[Double-blind treatment of 49 cases of chronic multiple sclerosis using hyperbaric oxygen]F Lhermitte, E Roullet, O Lyon-Caen, et al.
Annals of Neurology|August 1, 1995
An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)M Ragno, E Tournier-Lasserve, M G Fiori, et al.
Clinical Radiology|May 14, 2013
Natural history of cerebral dot-like cavernomasO Nikoubashman, M Wiesmann, E Tournier-Lasserve, et al.
Pageof 10

Showing results (61-70 of 100) with videos related to

Sort By:
Pageof 10
Genomics|December 1, 1996
A human homolog of bacterial acetolactate synthase genes maps within the CADASIL critical regionA Joutel, A Ducros, S Alamowitch, et al.
Stroke|February 5, 1999
Brain stem MRI signal abnormalities in CADASILH Chabriat, R Mrissa, C Levy, et al.
Bulletin De L'Academie Nationale De Medecine|March 23, 2001
[CADASIL: genetics and physiopathology]A Joutel, A François, H Chabriat, et al.
Archives of Neurology|March 1, 1989
Chronic myelopathies associated with human T-lymphotropic virus type I. A clinical, serologic, and immunovirologic study of ten patients in FranceO Gout, A Gessain, F Bolgert, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 4, 2011
[Genetic syndromes that mimic congenital infections: report of 2 cases]M Thibault, J Leydet, E Tournier-Lasserve, et al.
The New England Journal of Medicine|July 7, 2001
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channelA Ducros, C Denier, A Joutel, et al.
Revue Neurologique|October 14, 2018
A novel large deletion in CCM1 gene in a Tunisian familyF Tinsa, I Bel Hadj, F Riant, et al.
Revue Neurologique|January 1, 1986
[Double-blind treatment of 49 cases of chronic multiple sclerosis using hyperbaric oxygen]F Lhermitte, E Roullet, O Lyon-Caen, et al.
Annals of Neurology|August 1, 1995
An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)M Ragno, E Tournier-Lasserve, M G Fiori, et al.
Clinical Radiology|May 14, 2013
Natural history of cerebral dot-like cavernomasO Nikoubashman, M Wiesmann, E Tournier-Lasserve, et al.
Pageof 10