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Human Molecular Genetics|March 3, 2007
The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivoMarie Monet, Valérie Domenga, Barbara Lemaire, et al.
The Neuroradiology Journal|August 7, 2015
Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 geneFrancesco Garaci, Luisa Marsili, Florence Riant, et al.
Brain : a Journal of Neurology|March 19, 2009
Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domainMarie Monet-Leprêtre, Boris Bardot, Barbara Lemaire, et al.
Human Mutation|August 10, 2005
ATP1A2 mutations in 11 families with familial hemiplegic migraineFlorence Riant, Maurizio De Fusco, Paolo Aridon, et al.
Stroke|November 15, 2012
Antithrombotic therapy and bleeding risk in a prospective cohort study of patients with cerebral cavernous malformationsHans-Martin Schneble, Aicha Soumare, Dominique Hervé, et al.
European Journal of Neurology|June 23, 2026
Risk of Clinical Events in Presymptomatic Familial Cerebral Cavernous MalformationsConstantina Rodica Popa, Dominique Hervé, Nassira Alili, et al.
Ophthalmic Surgery, Lasers & Imaging Retina|June 22, 2018
Optical Coherence Tomography Angiography of Familial Retinal Arteriolar TortuosityAudrey Giocanti-Auregan, Alain Gaudric, Frédérique Buffon, et al.
Neurology. Genetics|April 17, 2023
Extension of the Clinicoradiologic Spectrum of Newly Described End-Truncating LAMB1 VariationsHélène Morel, Laurent Bailly, Cédric Urbanczyk, et al.
Scientific Reports|April 5, 2023
Impaired retinoic acid signaling in cerebral cavernous malformationsNastasja Grdseloff, Gwenola Boulday, Claudia J Rödel, et al.
Stroke|January 30, 2020
Novel Chronic Mouse Model of Cerebral Cavernous MalformationsCécile Cardoso, Minh Arnould, Coralie De Luca, et al.
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