Chabriat H - Search Results

1

Elderly CADASIL patients with intact neurological status.

Zhang R, Ouin E, Grosset L, Ighilkrim K, Lebenberg J, Guey S, François V, Tournier-Lasserve E, Jouvent E, Chabriat H. Zhang R, et al. Among authors: chabriat h. J Stroke. 2022 Sep;24(3):352-362. doi: 10.5853/jos.2022.01578. Epub 2022 Sep 30. J Stroke. 2022. PMID: 36221938 Free PMC article.

2

New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature.

Vérin M, Rolland Y, Landgraf F, Chabriat H, Bompais B, Michel A, Vahedi K, Martinet JP, Tournier-Lasserve E, Lemaitre MH, et al. Vérin M, et al. Among authors: chabriat h. J Neurol Neurosurg Psychiatry. 1995 Dec;59(6):579-85. doi: 10.1136/jnnp.59.6.579. J Neurol Neurosurg Psychiatry. 1995. PMID: 7500094 Free PMC article.

3

An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Ragno M, Tournier-Lasserve E, Fiori MG, Manca A, Patrosso MC, Ferlini A, Sirocchi G, Trojano L, Chabriat H, Salvi F. Ragno M, et al. Among authors: chabriat h. Ann Neurol. 1995 Aug;38(2):231-6. doi: 10.1002/ana.410380216. Ann Neurol. 1995. PMID: 7654071

4

Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus.

Chabriat H, Tournier-Lasserve E, Vahedi K, Leys D, Joutel A, Nibbio A, Escaillas JP, Iba-Zizen MT, Bracard S, Tehindrazanarivelo A, et al. Chabriat H, et al. Neurology. 1995 Jun;45(6):1086-91. doi: 10.1212/wnl.45.6.1086. Neurology. 1995. PMID: 7783868

5

Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL.

Ruchoux MM, Chabriat H, Bousser MG, Baudrimont M, Tournier-Lasserve E. Ruchoux MM, et al. Among authors: chabriat h. Stroke. 1994 Nov;25(11):2291-2. doi: 10.1161/01.str.25.11.2291. Stroke. 1994. PMID: 7974561 No abstract available.

6

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: chabriat h. Nature. 1996 Oct 24;383(6602):707-10. doi: 10.1038/383707a0. Nature. 1996. PMID: 8878478

7

A human homolog of bacterial acetolactate synthase genes maps within the CADASIL critical region.

Joutel A, Ducros A, Alamowitch S, Cruaud C, Domenga V, Maréchal E, Vahedi K, Chabriat H, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Among authors: chabriat h. Genomics. 1996 Dec 1;38(2):192-8. doi: 10.1006/geno.1996.0615. Genomics. 1996. PMID: 8954801

8

[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy)].

Chabriat H, Joutel A, Vahedi K, Iba-Zizen MT, Tournier-Lasserve E, Bousser MG. Chabriat H, et al. J Mal Vasc. 1996;21(5):277-82. J Mal Vasc. 1996. PMID: 9026542 Review. French.

9

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: chabriat h. Lancet. 1997 Nov 22;350(9090):1511-5. doi: 10.1016/S0140-6736(97)08083-5. Lancet. 1997. PMID: 9388399

10

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: chabriat h. Cerebrovasc Dis. 1998 Mar-Apr;8(2):97-101. doi: 10.1159/000015825. Cerebrovasc Dis. 1998. PMID: 9548007 Clinical Trial.

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