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The FEBS Journal|January 26, 2010
Recent insights into cerebral cavernous malformations: the molecular genetics of CCMFlorence Riant, Francoise Bergametti, Xavier Ayrignac, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 14, 2006
Frequency of retinal cavernomas in 60 patients with familial cerebral cavernomas: a clinical and genetic studyPierre Labauge, Valerie Krivosic, Christian Denier, et al.
European Journal of Human Genetics : EJHG|January 15, 2021
Extension of SKAT to multi-category phenotypes through a geometrical interpretationOzvan Bocher, Gaelle Marenne, Elisabeth Tournier-Lasserve, et al.
Stroke|April 9, 2005
Impaired cerebral vasoreactivity in a transgenic mouse model of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy arteriopathyPierre Lacombe, Charleen Oligo, Valérie Domenga, et al.
American Journal of Human Genetics|January 10, 2004
Pathogenic mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy differently affect Jagged1 binding and Notch3 activity via the RBP/JK signaling PathwayAnne Joutel, Marie Monet, Valérie Domenga, et al.
Trends in Molecular Medicine|March 20, 2013
Cerebral cavernous malformations: from CCM genes to endothelial cell homeostasisAndreas Fischer, Juan Zalvide, Eva Faurobert, et al.
Stroke|August 17, 2021
Hereditary Cerebral Small Vessel Diseases and Stroke: A Guide for Diagnosis and ManagementStéphanie Guey, Saskia A J Lesnik Oberstein, Elisabeth Tournier-Lasserve, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|December 4, 2018
Acute-Onset Ataxia and Transient Cerebellar Diffusion Restriction Associated with a PRRT2 MutationNicolas Legris, Olivier Chassin, Ghaidaa Nasser, et al.
Archives of Neurology|August 18, 2004
Migraine with aura and brain magnetic resonance imaging abnormalities in patients with CADASILKatayoun Vahedi, Hugues Chabriat, Claude Levy, et al.
The American Journal of Pathology|January 1, 2003
Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyMarie Magdeleine Ruchoux, Valérie Domenga, Peggy Brulin, et al.
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