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E Tournier

Showing results (101-110 of 155) with videos related to

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Journal of Perinatology : Official Journal of the California Perinatal Association|December 31, 2013
Fetal intracerebral hemorrhage and cataract: think COL4A1E Colin, L Sentilhes, A Sarfati, et al.
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.
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.
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.
Revue Neurologique|October 14, 2018
A novel large deletion in CCM1 gene in a Tunisian familyF Tinsa, I Bel Hadj, F Riant, et al.
Arthritis and Rheumatism|October 19, 1999
Poly(ADP-ribose) polymerase alleles in French Caucasians are associated neither with lupus nor with primary antiphospholipid syndrome. GRAID Research Group. Group for Research on Auto-Immune DisordersO Delrieu, M Michel, C Francès, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1995
New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical featureM Vérin, Y Rolland, F Landgraf, et al.
Pageof 16

Showing results (101-110 of 155) with videos related to

Sort By:
Pageof 16
Journal of Perinatology : Official Journal of the California Perinatal Association|December 31, 2013
Fetal intracerebral hemorrhage and cataract: think COL4A1E Colin, L Sentilhes, A Sarfati, et al.
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.
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.
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.
Revue Neurologique|October 14, 2018
A novel large deletion in CCM1 gene in a Tunisian familyF Tinsa, I Bel Hadj, F Riant, et al.
Arthritis and Rheumatism|October 19, 1999
Poly(ADP-ribose) polymerase alleles in French Caucasians are associated neither with lupus nor with primary antiphospholipid syndrome. GRAID Research Group. Group for Research on Auto-Immune DisordersO Delrieu, M Michel, C Francès, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1995
New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical featureM Vérin, Y Rolland, F Landgraf, et al.
Pageof 16