Onderzoeker
Lut Van Laer
- Disciplines:Pediatrie en neonatologie, Moleculaire en celbiologie, Systeembiologie, Verpleegkunde, Genetica
Affiliaties
- Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf16 jan 2009 → 30 nov 2010
Publicaties
1 - 10 van 27
- Familial aggregation of pure tone hearing thresholds in an aging European population(2013)
Auteurs: Jan-Jaap Hendrickx, Jeroen R Huyghe, Vedat Topsakal, Kelly Demeester, Thomas R Wienker, Lutgart Van Laer, Els Van Eyken, Erik Fransen, Elina Mäki-Torkko, Samuli Hannula, et al.
Pagina's: 838 - 844 - Agressive cardiovascular phenotype of aneurysms-osteoarthritis syndrome caused by pathogenic SMAD3 variants(2012)
Auteurs: Denise van der Linde, Ingrid MBH van de Laar, Aida M Bertoli-Avella, Rogier A Oldenburg, Jos A Bekkers, Francesco US Mattace-Raso, Anton H van den Meiracker, Adriaan Moelker, Fop van Kooten, Ingrid ME Frohn-Mulder, et al.
Pagina's: 397 - 403 - Vitamin K does not prevent soft tissue mineralization in a mouse model of pseudoxanthoma elasticum(2011)
Auteurs: Christopher Brampton, Yukiko Yamaguchi, Olivier Vanakker, Lutgart Van Laer, Li-Hsieh Chen, Manoj Thakore, Anne De Paepe, Viola Pomozi, Pal T Szabo, Ludovic Martin, et al.
Pagina's: 1810 - 1820 - Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys-Dietz syndromes(2011)
Auteurs: Machteld Baetens, Lutgart Van Laer, Kim De Leeneer, Jan Hellemans, Joachim De Schrijver, Hendrik Van de Voorde, Marjolijn Renard, Hal Dietz, Ronald V Lacro, Björn Menten, et al.
Pagina's: 1053 - 1062 - Involvement of T-cell receptor-beta alterations in the development of otosclerosis linked to OTSC2(2010)
Auteurs: I Schrauwen, Koen Venken, K Vanderstraeten, M Thys, JJ Hendrickx, E Fransen, Lutgart Van Laer, PJ Govaerts, M Verstreken, I Schatteman, et al.
Pagina's: 246 - 253 - Musculocontractural ehlers-danlos syndrome (former EDS type VIB) and adducted thumb clubfoot syndrome (ATCS) represent a single clinical entity caused by mutations in the dermatan-4-sulfotransferase 1 encoding CHST14 gene(2010)
Auteurs: Fransiska Malfait, Delfien Syx, Philip Vlummens, Sofie Symoens, Sheela Nampoothiri, Trinh Hermanns-Le, Lutgart Van Laer, Anne De Paepe
Pagina's: 1233 - 1239 - Het Marfansyndroom : een paradigma voor de studie van aorta-aneurysma's(2010)
Auteurs: Julie De Backer, Marjolijn Renard, Paul Coucke, Lutgart Van Laer, Anne De Paepe, Bart Loeys
Pagina's: 1024 - 1028 - Novel deletions causing pseudoxanthoma elasticum underscore the genomic instability of the ABCC6 region(2010)
Auteurs: Laura Costrop, Olivier Vanakker, Lutgart Van Laer, Olivier Le Saux, L Martin, N Chassaing, D Guerra, I Pasquali-Ronchetti, Paul Coucke, Anne De Paepe
Pagina's: 112 - 117 - Evaluation of host genetic and viral factors as surrogate markers for HTLV-1-associated myelopathy/tropical spastic paraparesis in Peruvian HTLV-1-infected patients(2010)
Auteurs: Michael Talledo, Giovanni Lopez, Jerone R Huyghe, Kristien Verdonck, Vanessa Adaui, Elsa Gonzalez, Ivan Best, Daniel Clark, Guido Vanham, Eduardo Gotuzzo, et al.
Pagina's: 460 - 466 - The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)(2010)
Auteurs: Delfien Syx, Fransiska Malfait, Lutgart Van Laer, Jan Hellemans, T Hermanns-Le, Andy Willaert, A Benmansour, Anne De Paepe, A Verloes
Pagina's: 79 - 88