Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

549 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis.
Joutel A, Favrole P, Labauge P, Chabriat H, Lescoat C, Andreux F, Domenga V, Cécillon M, Vahedi K, Ducros A, Cave-Riant F, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Among authors: bousser mg. Lancet. 2001 Dec 15;358(9298):2049-51. doi: 10.1016/S0140-6736(01)07142-2. Lancet. 2001. PMID: 11755616
Cadasil.
Chabriat H, Joutel A, Dichgans M, Tournier-Lasserve E, Bousser MG. Chabriat H, et al. Among authors: bousser mg. Lancet Neurol. 2009 Jul;8(7):643-53. doi: 10.1016/S1474-4422(09)70127-9. Lancet Neurol. 2009. PMID: 19539236 Review.
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia.
Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cécillion M, Marechal E, Maciazek J, Vayssiere C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Among authors: bousser mg. Nature. 1996 Oct 24;383(6602):707-10. doi: 10.1038/383707a0. Nature. 1996. PMID: 8878478
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia.
Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cécillion M, Maréchal E, Maciazek J, Vayssière C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Among authors: bousser mg. Ann N Y Acad Sci. 1997 Sep 26;826:213-7. doi: 10.1111/j.1749-6632.1997.tb48472.x. Ann N Y Acad Sci. 1997. PMID: 9329692 Review.
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients.
Joutel A, Vahedi K, Corpechot C, Troesch A, Chabriat H, Vayssière C, Cruaud C, Maciazek J, Weissenbach J, Bousser MG, Bach JF, Tournier-Lasserve E. Joutel A, et al. Among authors: bousser mg. Lancet. 1997 Nov 22;350(9090):1511-5. doi: 10.1016/S0140-6736(97)08083-5. Lancet. 1997. PMID: 9388399
Patterns of MRI lesions in CADASIL.
Chabriat H, Levy C, Taillia H, Iba-Zizen MT, Vahedi K, Joutel A, Tournier-Lasserve E, Bousser MG. Chabriat H, et al. Among authors: bousser mg. Neurology. 1998 Aug;51(2):452-7. doi: 10.1212/wnl.51.2.452. Neurology. 1998. PMID: 9710018 Clinical Trial.
De novo mutation in the Notch3 gene causing CADASIL.
Joutel A, Dodick DD, Parisi JE, Cecillon M, Tournier-Lasserve E, Bousser MG. Joutel A, et al. Among authors: bousser mg. Ann Neurol. 2000 Mar;47(3):388-91. Ann Neurol. 2000. PMID: 10716263
[Unusual disorder: CADASIL].
Vahedi K, Bousser MG. Vahedi K, et al. Among authors: bousser mg. Encephale. 2000 Apr;26 Spec No 3:3-6. Encephale. 2000. PMID: 10858924 French. No abstract available.
549 results