P. Labauge

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...

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...

Spanish families with cavernous angiomas do not share the Hispano- American CCM1 haplotype

JUNG, H, LABAUGE, P, LABERGE, S, MARECHAL, E, TOURNIER-LASSERVE, E, LUCAS, M, ...

Isolated spastic paraparesis leading to diagnosis of Friedreich's ataxia

CASTELNOVO, G, BIOLSI, B, BARBAUD, A, LABAUGE, P, SCHMITT, M

Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum is different from that observed in familial cases

Depienne, C, Tallaksen, C, Lephay, J Y, Bricka, B, Poea‐Guyon, S, Fontaine, B, ...