K. Vahedi

Publication List Details

Period

2008 - 2008

Number

14

Co-Authors

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.

Ducros, A, Denier, C, Joutel, A, Vahedi, K, Michel, A, Darcel, F, ...

Familial hemiplegic migraine (HM) is an autosomal dominant migraine with aura. In 20% of HM families, HM is associated with a mild permanent cerebellar ataxia (PCA). The CACNA1A gene encoding the...

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.

Ducros, A, Denier, C, Joutel, A, Vahedi, K, Michel, A, Darcel, F, ...

Familial hemiplegic migraine (HM) is an autosomal dominant migraine with aura. In 20% of HM families, HM is associated with a mild permanent cerebellar ataxia (PCA). The CACNA1A gene encoding the...

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Ieukoencephalopathy, Genetic Homogeneity, and Mapping of the Locus within a 2-cM Interval

Ducros, A., Nagy, T., Alamowitch, S., Nibbio, A., Joutel, A., Vahedi, K., ...

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a recently identified autosomal dominant cerebral arteriopathy characterized by the recurrence...

Genetic Heterogeneity of Familial Hemiplegic Migraine

Joutel, A., Ducros, A., Vahedi, K., Labauge, P., Delrieu, O., Pinsard, N., ...

Familial hemiplegic migraine (FHM) is an autosomal dominant variety of migraine with aura. We previously mapped a gene responsible for this disorder to the short arm of chromosome 19, within a 30-cM...

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss family.

Jung, H H, Bassetti, C, Tournier-Lasserve, E, Vahedi, K, Arnaboldi, M, Arifi, V B, ...

This paper reports a Swiss family affected by a cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) linked to chromosome 19q12. In three generations...

Horizontal eye movement disorders after posterior vermis infarctions.

Vahedi, K, Rivaud, S, Amarenco, P, Pierrot-Deseilligny, C

The horizontal saccade, smooth pursuit, and vestibulo-ocular reflex gains were recorded in 19 patients with cerebellar infarction documented with MRI, and in a group of control subjects. Bilateral...

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, ...

A survey was carried out on a large family presenting the symptoms of familial arteriopathy (CADASIL) recently mapped to chromosome 19. This is characterised clinically by recurrent subcortical...

Intracranial dural fistula as a cause of diffuse MR enhancement of the cervical spinal cord

Bousson, V., Brunereau, L., Vahedi, K., Chapot, R.

Spinal MR findings are reported in a patient with progressive myelopathy and intracranial dural arteriovenous fistula draining into spinal veins. Associated with previously reported abnormalities on...

Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q

Notelet, L, Chapon, F, Khoury, S, Vahedi, K, Chodkiewicz, J, Courtheoux, P, ...

OBJECTIVES—To characterise clinically a large French family affected with cerebral cavernomas and to check for linkage of this condition to chromosome 7.
METHODS—A family, originating from...

Orgasmic headache and middle cerebral artery dissection

Szatmary, Z, Boukobza, M, Vahedi, K, Stapf, C, Houdart, E, Bousser, M G

A patient with a 20 year history of primary orgasmic headache is described who, after suffering an unusually severe episode of orgasmic headache was found to have a middle cerebral artery dissection....