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Journal of Hypertension|August 1, 2018
Home blood pressure measurement and digital health: communication technologies create a new contextNicolas Postel-Vinay, Guillaume Bobrie, Sébastien Savard, et al.
Current Hypertension Reports|February 3, 2017
Renal Artery Stenosis in Patients with Resistant Hypertension: Stent It or Not?Patricia Van der Niepen, Patrick Rossignol, Jean-Philippe Lengelé, et al.
Kardiologia Polska|June 24, 2021
Fibromuscular dysplasia: its various phenotypes in everyday practice in 2021Patricia Van der Niepen, Tom Robberechts, Hannes Devos, et al.
Human Molecular Genetics|May 2, 2013
Venous malformation-causative TIE2 mutations mediate an AKT-dependent decrease in PDGFBMelanie Uebelhoer, Marjut Nätynki, Jaakko Kangas, et al.
Archives of Dermatology|November 18, 2009
Elevated D-dimer level in the differential diagnosis of venous malformationsAnne Dompmartin, Fanny Ballieux, Pascal Thibon, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 19, 2004
A gene encoding a putative FAD-dependent L-2-hydroxyglutarate dehydrogenase is mutated in L-2-hydroxyglutaric aciduriaRim Rzem, Maria Veiga-da-Cunha, Gaëtane Noël, et al.
Current Hypertension Reports|June 11, 2014
Renal denervation after Symplicity HTN-3: an updateAlexandre Persu, Yu Jin, Fadl Elmula Mohamed Fadl Elmula, et al.
Journal of Cell Science|February 24, 2012
Ligand oligomerization state controls Tie2 receptor trafficking and angiopoietin-2-specific responsesRiikka Pietilä, Marjut Nätynki, Tuomas Tammela, et al.
Genes|April 28, 2023
<i>SATB2</i>-Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature ReviewMatheus de Mello Copelli, Eleonore Pairet, Milena Atique-Tacla, et al.
Orphanet Journal of Rare Diseases|June 15, 2014
Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutationsMuriel de la Dure-Molla, Mickael Quentric, Paulo Marcio Yamaguti, et al.
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