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Page 1
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: vahedi k. Neurology. 1998 Aug;51(2):452-7. doi: 10.1212/wnl.51.2.452. Neurology. 1998. PMID: 9710018 Clinical Trial.
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: vahedi k. 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: vahedi k. Lancet. 1997 Nov 22;350(9090):1511-5. doi: 10.1016/S0140-6736(97)08083-5. Lancet. 1997. PMID: 9388399
Cognitive alterations in non-demented CADASIL patients.
Taillia H, Chabriat H, Kurtz A, Verin M, Levy C, Vahedi K, Tournier-Lasserve E, Bousser MG. Taillia H, et al. Among authors: vahedi k. Cerebrovasc Dis. 1998 Mar-Apr;8(2):97-101. doi: 10.1159/000015825. Cerebrovasc Dis. 1998. PMID: 9548007 Clinical Trial.
126 results