Joutel Anne
Joutel Anne
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Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
A Joutel, C Corpechot, A Ducros, K Vahedi, H Chabriat, P Mouton, ...
Nature 383 (6602), 707-710, 1996
H Chabriat, A Joutel, M Dichgans, E Tournier-Lasserve, MG Bousser
The Lancet Neurology 8 (7), 643-653, 2009
Clinical spectrum of CADASIL: a study of 7 families
H Chabriat, K Vahedi, MG Bousser, MT Iba-Zizen, A Joutel, A Nibbio, ...
The Lancet 346 (8980), 934-939, 1995
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12
E Tournier-Lasserve, A Joutel, J Melki, J Weissenbach, GM Lathrop, ...
Nature genetics 3 (3), 256-259, 1993
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients
A Joutel, K Vahedi, C Corpechot, A Troesch, H Chabriat, C Vayssière, ...
The Lancet 350 (9090), 1511-1515, 1997
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel
A Ducros, C Denier, A Joutel, M Cecillon, C Lescoat, K Vahedi, F Darcel, ...
New England Journal of Medicine 345 (1), 17-24, 2001
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients
A Joutel, F Andreux, S Gaulis, V Domenga, M Cecillon, N Battail, N Piga, ...
The Journal of clinical investigation 105 (5), 597-605, 2000
Notch3 is required for arterial identity and maturation of vascular smooth muscle cells
V Domenga, P Fardoux, P Lacombe, M Monet, J Maciazek, LT Krebs, ...
Genes & development 18 (22), 2730-2735, 2004
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas
S Laberge-le Couteulx, HH Jung, P Labauge, JP Houtteville, C Lescoat, ...
Nature genetics 23 (2), 189-193, 1999
A gene for familial hemiplegic migraine maps to chromosome 19
A Joutel, MG Bousser, V Biousse, P Labauge, H Chabriat, A Nibbio, ...
Nature genetics 5 (1), 40-45, 1993
Patterns of MRI lesions in CADASIL
H Chabriat, C Levy, H Taillia, MT Iba-Zizen, K Vahedi, A Joutel, ...
Neurology 51 (2), 452-457, 1998
Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study.
M Baudrimont, F Dubas, A Joutel, E Tournier-Lasserve, MG Bousser
Stroke 24 (1), 122-125, 1993
Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel disease
A Joutel, M Monet-Leprêtre, C Gosele, C Baron-Menguy, A Hammes, ...
The Journal of clinical investigation 120 (2), 433-445, 2010
Characterization of Notch3‐deficient mice: Normal embryonic development and absence of genetic interactions with a Notch1 mutation
LT Krebs, Y Xue, CR Norton, JP Sundberg, P Beatus, U Lendahl, A Joutel, ...
genesis 37 (3), 139-143, 2003
Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis
A Joutel, P Favrole, P Labauge, H Chabriat, C Lescoat, F Andreux, ...
The Lancet 358 (9298), 2049-2051, 2001
Mapping of a second locus for familial hemiplegic migraine to 1q21–q23 and evidence of further heterogeneity
A Ducros, A Joutel, M Cecillon, E Tournier‐Lasserve, K Vahedi, ...
Annals of Neurology: Official Journal of the American Neurological …, 1997
Notch signalling pathway and human diseases
A Joutel, E Tournier-Lasserve
Seminars in cell & developmental biology 9 (6), 619-625, 1998
High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2
C Denier, A Ducros, K Vahedi, A Joutel, P Thierry, A Ritz, G Castelnovo, ...
Neurology 52 (9), 1816-1816, 1999
Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
MM Ruchoux, V Domenga, P Brulin, J Maciazek, S Limol, ...
The American journal of pathology 162 (1), 329-342, 2003
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia
A Ducros, C Denier, A Joutel, K Vahedi, A Michel, F Darcel, M Madigand, ...
The American Journal of Human Genetics 64 (1), 89-98, 1999
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