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A Joutel

Showing results (31-40 of 42) with videos related to

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Neurology|June 1, 1995
Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locusH Chabriat, E Tournier-Lasserve, K Vahedi, et al.
Annals of Neurology|December 24, 1997
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneityA Ducros, A Joutel, K Vahedi, et al.
Nature Genetics|October 3, 1999
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomasS Laberge-le Couteulx, H H Jung, P Labauge, et al.
Lancet (London, England)|December 6, 1997
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patientsA Joutel, K Vahedi, C Corpechot, et al.
Lancet (London, England)|January 5, 2002
Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosisA Joutel, P Favrole, P Labauge, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 27, 2008
Notch3 is a major regulator of vascular tone in cerebral and tail resistance arteriesE J Belin de Chantemèle, K Retailleau, F Pinaud, et al.
Neurology|January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathyK Vahedi, P Massin, J-P Guichard, et al.
American Journal of Human Genetics|January 23, 1999
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxiaA Ducros, C Denier, A Joutel, et al.
Annals of the New York Academy of Sciences|November 5, 1997
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementiaA Joutel, C Corpechot, A Ducros, et al.
Nature|October 24, 1996
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementiaA Joutel, C Corpechot, A Ducros, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Neurology|June 1, 1995
Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locusH Chabriat, E Tournier-Lasserve, K Vahedi, et al.
Annals of Neurology|December 24, 1997
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneityA Ducros, A Joutel, K Vahedi, et al.
Nature Genetics|October 3, 1999
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomasS Laberge-le Couteulx, H H Jung, P Labauge, et al.
Lancet (London, England)|December 6, 1997
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patientsA Joutel, K Vahedi, C Corpechot, et al.
Lancet (London, England)|January 5, 2002
Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosisA Joutel, P Favrole, P Labauge, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 27, 2008
Notch3 is a major regulator of vascular tone in cerebral and tail resistance arteriesE J Belin de Chantemèle, K Retailleau, F Pinaud, et al.
Neurology|January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathyK Vahedi, P Massin, J-P Guichard, et al.
American Journal of Human Genetics|January 23, 1999
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxiaA Ducros, C Denier, A Joutel, et al.
Annals of the New York Academy of Sciences|November 5, 1997
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementiaA Joutel, C Corpechot, A Ducros, et al.
Nature|October 24, 1996
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementiaA Joutel, C Corpechot, A Ducros, et al.
Pageof 5