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A Joutel

Showing results (11-20 of 42) with videos related to

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Mechanisms of Development|September 3, 2002
Krit1/cerebral cavernous malformation 1 mRNA is preferentially expressed in neurons and epithelial cells in embryo and adultC Denier, J-M Gasc, F Chapon, et al.
Bulletin De L'Academie Nationale De Medecine|March 23, 2001
[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): clinical features and neuroimaging]H Chabriat, A Joutel, K Vahedi, et al.
Journal Des Maladies Vasculaires|January 1, 1996
[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy)]H Chabriat, A Joutel, K Vahedi, et al.
Revue Neurologique|July 1, 1997
[CADASIS. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalophathy]H Chabriat, A Joutel, K Vahedi, et al.
Annals of Neurology|March 15, 2000
De novo mutation in the Notch3 gene causing CADASILA Joutel, D D Dodick, J E Parisi, et al.
European Radiology|April 16, 1998
Perichiasmatic granuloma occuring after radical mastoidectomy: MR findingsH Djouhri, K Marsot-Dupuch, A Joutel, et al.
Neuropediatrics|November 24, 1999
Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1B Echenne, A Ducros, F Rivier, et al.
Neurology|August 26, 1998
Patterns of MRI lesions in CADASILH Chabriat, C Levy, H Taillia, et al.
The Journal of Clinical Investigation|March 11, 2000
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patientsA Joutel, F Andreux, S Gaulis, et al.
Annals of Neurology|March 1, 1995
A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19pK Vahedi, A Joutel, P Van Bogaert, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
Mechanisms of Development|September 3, 2002
Krit1/cerebral cavernous malformation 1 mRNA is preferentially expressed in neurons and epithelial cells in embryo and adultC Denier, J-M Gasc, F Chapon, et al.
Bulletin De L'Academie Nationale De Medecine|March 23, 2001
[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): clinical features and neuroimaging]H Chabriat, A Joutel, K Vahedi, et al.
Journal Des Maladies Vasculaires|January 1, 1996
[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy)]H Chabriat, A Joutel, K Vahedi, et al.
Revue Neurologique|July 1, 1997
[CADASIS. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalophathy]H Chabriat, A Joutel, K Vahedi, et al.
Annals of Neurology|March 15, 2000
De novo mutation in the Notch3 gene causing CADASILA Joutel, D D Dodick, J E Parisi, et al.
European Radiology|April 16, 1998
Perichiasmatic granuloma occuring after radical mastoidectomy: MR findingsH Djouhri, K Marsot-Dupuch, A Joutel, et al.
Neuropediatrics|November 24, 1999
Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1B Echenne, A Ducros, F Rivier, et al.
Neurology|August 26, 1998
Patterns of MRI lesions in CADASILH Chabriat, C Levy, H Taillia, et al.
The Journal of Clinical Investigation|March 11, 2000
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patientsA Joutel, F Andreux, S Gaulis, et al.
Annals of Neurology|March 1, 1995
A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19pK Vahedi, A Joutel, P Van Bogaert, et al.
Pageof 5