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A Joutel

Showing results (21-30 of 42) with videos related to

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American Journal of Human Genetics|December 1, 1994
Genetic heterogeneity of familial hemiplegic migraineA Joutel, A Ducros, K Vahedi, 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|January 1, 1994
[Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19]A Joutel, M G Bousser, V Biousse, 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.
Neurology|May 10, 2000
Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASILA Joutel, H Chabriat, K Vahedi, et al.
Stroke|February 5, 1999
Brain stem MRI signal abnormalities in CADASILH Chabriat, R Mrissa, C Levy, et al.
Nature Genetics|September 1, 1993
A gene for familial hemiplegic migraine maps to chromosome 19A Joutel, M G Bousser, V Biousse, et al.
Bulletin De L'Academie Nationale De Medecine|March 23, 2001
[CADASIL: genetics and physiopathology]A Joutel, A François, H Chabriat, et al.
Lancet (London, England)|October 7, 1995
Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyH Chabriat, K Vahedi, M T Iba-Zizen, et al.
Nature Genetics|March 1, 1993
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12E Tournier-Lasserve, A Joutel, J Melki, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|December 1, 1994
Genetic heterogeneity of familial hemiplegic migraineA Joutel, A Ducros, K Vahedi, 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|January 1, 1994
[Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19]A Joutel, M G Bousser, V Biousse, 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.
Neurology|May 10, 2000
Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASILA Joutel, H Chabriat, K Vahedi, et al.
Stroke|February 5, 1999
Brain stem MRI signal abnormalities in CADASILH Chabriat, R Mrissa, C Levy, et al.
Nature Genetics|September 1, 1993
A gene for familial hemiplegic migraine maps to chromosome 19A Joutel, M G Bousser, V Biousse, et al.
Bulletin De L'Academie Nationale De Medecine|March 23, 2001
[CADASIL: genetics and physiopathology]A Joutel, A François, H Chabriat, et al.
Lancet (London, England)|October 7, 1995
Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyH Chabriat, K Vahedi, M T Iba-Zizen, et al.
Nature Genetics|March 1, 1993
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12E Tournier-Lasserve, A Joutel, J Melki, et al.
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