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  1. Article

    Open Access

    3.3 Effect of Celiprolol on Prevention of Cardiovascular Events in Vascular Ehlers-Danlos Syndrome

    Vascular Ehlers-Danlos syndrome (vEDS) is a rare severe genetic disease which results from mutations in the gene encoding type III procollagen (COL3A1), characterized by vascular and/or hollow organic ruptures...

    K. T. Ong, J. Perdu, H. Plauchu, J. De Backer, A. De Paepe, J. Emmerich in Artery Research (2009)

  2. Article

    Open Access

    01.02 Geometric and Elastic Properties of the Common Carotid Artery in Vascular Ehlers-Danlos Syndrome Patients with Identified COL3A1 Mutations

    Vascular Ehlers-Danlos syndrome (vEDS), an autosomal dominant inherited disorder of connective tissue, results from mutations in the gene encoding type III procollagen (COL3A1), can present with spontaneous ar...

    K. T. Ong, S. Laurent, J. Perdu, H. Plauchu, D. Germain, P. Collignon in Artery Research (2008)

  3. No Access

    Chapter

    Dysplasie fibromusculaire des artères rénales: données récentes

    La dysplasie fibromusculaire (DFM) est un groupe de maladies non athéroscléreuses et non inflammatoires de la musculeuse des parois artérielles, qui atteignent les artères de petit et moyen calibres, particuli...

    P.-R Plouin, L. Weis, C. Lepoutre, L. Amar in Radiologie interventionnelle des artères r… (2008)

  4. No Access

    Article

    Inheritance of arterial lesions in renal fibromuscular dysplasia

    We have previously shown that patients with renal fibromuscular dysplasia (FMD) have asymptomatic carotid lesions and that familial forms may occur. The objective of this study was to test whether carotid lesi...

    J Perdu, P Boutouyrie, C Bourgain, N Stern, B Laloux in Journal of Human Hypertension (2007)