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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 adult
C 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 CADASIL
A Joutel, D D Dodick, J E Parisi, et al.
European Radiology
|
April 16, 1998
Perichiasmatic granuloma occuring after radical mastoidectomy: MR findings
H 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 1
B Echenne, A Ducros, F Rivier, et al.
Neurology
|
August 26, 1998
Patterns of MRI lesions in CADASIL
H 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 patients
A Joutel, F Andreux, S Gaulis, et al.
Annals of Neurology
|
March 1, 1995
A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p
K Vahedi, A Joutel, P Van Bogaert, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 42) with videos related to
Sort By:
Page
of 5
Mechanisms of Development
|
September 3, 2002
Krit1/cerebral cavernous malformation 1 mRNA is preferentially expressed in neurons and epithelial cells in embryo and adult
C 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 CADASIL
A Joutel, D D Dodick, J E Parisi, et al.
European Radiology
|
April 16, 1998
Perichiasmatic granuloma occuring after radical mastoidectomy: MR findings
H 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 1
B Echenne, A Ducros, F Rivier, et al.
Neurology
|
August 26, 1998
Patterns of MRI lesions in CADASIL
H 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 patients
A Joutel, F Andreux, S Gaulis, et al.
Annals of Neurology
|
March 1, 1995
A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p
K Vahedi, A Joutel, P Van Bogaert, et al.
Page
of 5