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Article
Open Access3.3 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...
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Article
Open Access01.02 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...
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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...
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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...