Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author exact 001997095614 cql: author exact 001992218130 Add to list Journal Article A1 SAMHD1 compound heterozygous rare variants associated with moyamoya and mitral valve disease in the absence of other features of Aicardi-Goutières syndrome Aamuktha R. Karla, Amelie Pinard, Maura L. Boerio, Dimitri Hemelsoet (UGent) , Simon Tavernier (UGent) , Michel De Pauw (UGent) , Elke Vereecke (UGent) , Stuart Fraser, Michael J. Bamshad, Dongchuan Guo, et al. (2024) AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 194(4). Add to list Journal Article A1 open access Shortcutting the diagnostic odyssey : the multidisciplinary program for undiagnosed rare diseases in adults (UD-PrOZA) Nika Schuermans (UGent) , Dimitri Hemelsoet (UGent) , Wim Terryn, Sanne Steyaert (UGent) , Rudy Van Coster (UGent) , Paul Coucke (UGent) , Wouter Steyaert, Bert Callewaert (UGent) , Elke Bogaert (UGent) , Patrick Verloo (UGent) , et al. (2022) ORPHANET JOURNAL OF RARE DISEASES. 17(1). Add to list Conference Paper C3 Fibromuscular dysplasia : results of a multicentre study in Flanders Marie De Groote (UGent) , Dimitri Hemelsoet (UGent) , Patricia Van der Niepen, Bert Callewaert (UGent) , Frank Vermassen (UGent) , Jean-Marie Billiouw, An De Vriese, Jan Donck and Tine De Backer (UGent) (2017) ACTA CARDIOLOGICA. 72(1). p.113-113 Add to list Journal Article A1 Fibromuscular dysplasia : results of a multicentre study in Flanders Marie De Groote (UGent) , Patricia Van der Niepen, Dimitri Hemelsoet (UGent) , Bert Callewaert (UGent) , Frank Vermassen (UGent) , Jean-Marie Billiouw, An De Vriese, Jan Donck and Tine De Backer (UGent) (2017) VASA-EUROPEAN JOURNAL OF VASCULAR MEDICINE. 46(3). p.211-218