Christelle Lescoat

Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas

A. Joutel, E. Maréchal, J. Bach, 1999, Nature Genetics.

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.

E. Vicaut, A. Joutel, A. Ducros, 2001, The New England journal of medicine.

Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis

H. Chabriat, A. Joutel, A. Ducros, 2001, The Lancet.

Identification of CACNA1A large deletions in four patients with episodic ataxia

A. Toutain, K. Vahedi, E. Tournier-Lasserve, 2010, neurogenetics.

Krit1/cerebral cavernous malformation 1 mRNA is preferentially expressed in neurons and epithelial cells in embryo and adult

F. Chapon, A. Joutel, V. Domenga, 2002, Mechanisms of Development.