Vahedi K - Search Results

1

Migraine with aura and brain magnetic resonance imaging abnormalities in patients with CADASIL.

Vahedi K, Chabriat H, Levy C, Joutel A, Tournier-Lasserve E, Bousser MG. Vahedi K, et al. Arch Neurol. 2004 Aug;61(8):1237-40. doi: 10.1001/archneur.61.8.1237. Arch Neurol. 2004. PMID: 15313840

2

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. Among authors: vahedi k. Neurology. 1995 Jun;45(6):1086-91. doi: 10.1212/wnl.45.6.1086. Neurology. 1995. PMID: 7783868

3

[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. Among authors: vahedi k. J Mal Vasc. 1996;21(5):277-82. J Mal Vasc. 1996. PMID: 9026542 Review. French.

4

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.

5

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.

6

Differential diagnosis of a vascular leukoencephalopathy within a CADASIL family: use of skin biopsy electron microscopy study and direct genotypic screening.

Furby A, Vahedi K, Force M, Larrouy S, Ruchoux MM, Joutel A, Tournier-Lasserve E. Furby A, et al. Among authors: vahedi k. J Neurol. 1998 Nov;245(11):734-40. doi: 10.1007/s004150050277. J Neurol. 1998. PMID: 9808243

7

Brain stem MRI signal abnormalities in CADASIL.

Chabriat H, Mrissa R, Levy C, Vahedi K, Taillia H, Iba-Zizen MT, Joutel A, Tournier-Lasserve E, Bousser MG. Chabriat H, et al. Among authors: vahedi k. Stroke. 1999 Feb;30(2):457-9. doi: 10.1161/01.str.30.2.457. Stroke. 1999. PMID: 9933287

8

Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A gene.

Chabriat H, Vahedi K, Clark CA, Poupon C, Ducros A, Denier C, Le Bihan D, Bousser MG. Chabriat H, et al. Among authors: vahedi k. Neurology. 2000 Jan 25;54(2):510-2. doi: 10.1212/wnl.54.2.510. Neurology. 2000. PMID: 10668728

9

Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASIL.

Joutel A, Chabriat H, Vahedi K, Domenga V, Vayssière C, Ruchoux MM, Lucas C, Leys D, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Among authors: vahedi k. Neurology. 2000 May 9;54(9):1874-5. doi: 10.1212/wnl.54.9.1874. Neurology. 2000. PMID: 10802807 No abstract available.

10

[Unusual disorder: CADASIL].

Vahedi K, Bousser MG. Vahedi K, et al. Encephale. 2000 Apr;26 Spec No 3:3-6. Encephale. 2000. PMID: 10858924 French. No abstract available.

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