A. Ducros

Le mouvement social actuel dans le protestantisme Français / (1901)

Ducros, A.

Thesis (doctoral)--Université de Paris, 1901.

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...