Researcher
Martine Biervliet
- Keywords:Medicine
Affiliations
- Clinical sciences (Department)
Member
From1 Jan 2017 → 31 Dec 2018 - Surgical clinical sciences (Department)
Member
From1 Feb 2016 → 31 Jan 2018 - Medical Genetics (Department)
Member
From1 Aug 2011 → 28 Feb 2019
Publications
1 - 5 of 5
- Prolonged Right Ventricular Ejection Delay in Brugada Syndrome Depends on the Type of SCN5A Variant - Electromechanical Coupling Through Tissue Velocity Imaging as a Bridge Between Genotyping and Phenotyping(2017)
Authors: Sophie Van Malderen, Dorien Daneels, Dirk Kerkhove, Uschi Peeters, Dominic A M J Theuns, Steven Droogmans, Guy Van Camp, Caroline Weytjens, Martine Biervliet, Maryse Bonduelle, et al.
Pages: 53-61 - Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia(2015)
Authors: Sofie Symoens, Aileen M Barnes, Charlotte Gistelinck, Fransiska Malfait, Brecht Guillemyn, Wouter Steyaert, Delfien Syx, Sanne D'hondt, Martine Biervliet, Julie De Backer, et al.
Pages: 521-534 - New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update(2014)
Authors: Claire Laure Navarro, Vera Esteves-Vieira, Sébastien Courrier, Amandine Boyer, Thuy Duong Nguyen, Le Thi Thanh Huong, Peter Meinke, Winnie Schröder, Valérie Cormier-Daire, Yves Sznajer, et al.
Pages: 1002-1011 - SCN5A mutation analysis in 147 Brugada syndrome probands(2014)
Authors: Sonia Van Dooren, Uschi Peeters, Dorien Daneels, Pedro Brugada, Sophie Van Malderen, Gudrun Pappaert, Marije Meuwissen, Inge Timmermans, Martine Biervliet, D. Raimundi, et al.
Pages: 112-112 - The mutation spectrum in RECQL4 diseases(2009)
Authors: A. Siitonen, J Sotkasiira, Martine Biervliet, A Benmansour, Y Capri, V. Cormier-Daire, B Crandall, K Hannula-Jouppi, R.c. Hennekam, Daniela Herzog, et al.
Pages: 151-158