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Orphanet Journal of Rare Diseases|December 10, 2025
Personalized sirolimus regimen for vascular malformations: a retrospective analysis of VASE cohortEmmanuel Seront, An Van Damme, Julien Coulie, et al.
Expert Review of Clinical Pharmacology|March 8, 2026
Current and emerging pharmacotherapies for treating vascular malformationsEmmanuel Seront, An Van Damme, Julien Coulie, et al.
Acta Cardiologica|September 17, 2004
Recent insights in the development of organ damage caused by hypertensionAlexandre Persu, Jean-François De Plaen
Hypertension Research : Official Journal of the Japanese Society of Hypertension|April 18, 2014
Use of ambulatory blood pressure measurement in the definition of resistant hypertension: a review of the evidenceAlexandre Persu, Eoin O'Brien, Paolo Verdecchia
Critical Reviews in Oncology/Hematology|December 10, 2016
Routine use of gene panel testing in hereditary breast cancer should be performed with cautionCedric van Marcke, Anne De Leener, Martine Berlière, et al.
Gene Expression Patterns : GEP|April 1, 2004
Glomulin is predominantly expressed in vascular smooth muscle cells in the embryonic and adult mouseBrendan A S McIntyre, Pascal Brouillard, Virginie Aerts, et al.
Orphanet Journal of Rare Diseases|July 9, 2021
A review of mechanisms of disease across PIK3CA-related disorders with vascular manifestationsGuillaume Canaud, Adrienne M Hammill, Denise Adams, et al.
Current Opinion in Nephrology and Hypertension|July 30, 2013
Renal denervation in the management of resistant hypertension: current evidence and perspectivesYu Jin, Alexandre Persu, Jan A Staessen
European Journal of Human Genetics : EJHG|June 25, 2002
Locus for susceptibility for familial capillary malformation ('port-wine stain') maps to 5qIiro Eerola, Laurence M Boon, Shoji Watanabe, et al.
Acta Dermato-Venereologica|March 26, 2004
Progressive hyperpigmentation and generalized lentiginosis without associated systemic symptoms: a rare hereditary pigmentation disorder in south-east GermanyLivia Zanardo, Wilhelm Stolz, Gerd Schmitz, et al.
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