C. Denier

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...

Mutations within the MGC4607 Gene Cause Cerebral Cavernous Malformations

Denier, C., Goutagny, S., Labauge, P., Krivosic, V., Arnoult, M, Cousin, A., ...

Cerebral cavernous malformations (CCM) are hamartomatous vascular malformations characterized by abnormally enlarged capillary cavities without intervening brain parenchyma. They cause seizures and...

Mutations within the Programmed Cell Death 10 Gene Cause Cerebral Cavernous Malformations

Bergametti, F., Denier, C., Labauge, P., Arnoult, M., Boetto, S., Clanet, M., ...

Cerebral cavernous malformations (CCMs) are hamartomatous vascular malformations characterized by abnormally enlarged capillary cavities without intervening brain parenchyma. They cause seizures and...

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...