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Hypertension (Dallas, Tex. : 1979)|March 26, 2014
Eligibility for renal denervation: experience at 11 European expert centersAlexandre Persu, Yu Jin, Marie Baelen, et al.Cardiovascular Research|March 19, 2021
Current progress in clinical, molecular, and genetic aspects of adult fibromuscular dysplasiaAlexandre Persu, Piotr Dobrowolski, Heather L Gornik, et al.Lancet (London, England)|May 19, 2021
Ultrasound renal denervation for hypertension resistant to a triple medication pill (RADIANCE-HTN TRIO): a randomised, multicentre, single-blind, sham-controlled trialMichel Azizi, Kintur Sanghvi, Manish Saxena, et al.Vascular Medicine (London, England)|January 17, 2019
First International Consensus on the diagnosis and management of fibromuscular dysplasiaHeather L Gornik, Alexandre Persu, David Adlam, et al.Circulation|July 9, 2017
Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK SignalingMustapha Amyere, Nicole Revencu, Raphaël Helaers, et al.Hypertension (Dallas, Tex. : 1979)|July 9, 2020
Pregnancy-Related Complications in Patients With Fibromuscular Dysplasia: A Report From the European/International Fibromuscular Dysplasia RegistryMarco Pappaccogli, Aleksander Prejbisz, Simina Ciurică, et al.Journal of Hypertension|January 15, 2019
First international consensus on the diagnosis and management of fibromuscular dysplasiaHeather L Gornik, Alexandre Persu, David Adlam, et al.Cardiovascular Diabetology|March 23, 2025
Exploring the impact of metabolic comorbidities on epicardial adipose tissue in heart failure with preserved ejection fractionNassiba Menghoum, Maria Chiara Badii, Martin Leroy, et al.Cardiovascular Research|April 14, 2020
The European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI)-clinical phenotypes and their predictors based on a cohort of 1000 patientsMarco Pappaccogli, Silvia Di Monaco, Ewa Warchoł-Celińska, et al.Neuron|December 23, 2018
Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen MalformationDaniel Duran, Xue Zeng, Sheng Chih Jin, et al.Pageof 32