E. Tournier-Lasserve

Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASIL

H. Chabriat, A. Joutel, K. Vahedi, 2000, Neurology.

Monogenic cerebral small‐vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of Neurology

J. Finsterer, C. Enzinger, M. Mancuso, 2020, European journal of neurology.

Cognitive Alterations in Non-Demented CADASIL Patients

M. Vérin, H. Chabriat, K. Vahedi, 1998, Cerebrovascular Diseases.

SPECT study of a German CADASIL family

H. Chabriat, H. Goebel, E. Tournier-Lasserve, 1998, Neurology.