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="Jedlickova, Ivana" or (type exact bookEditor and editor="Jedlickova, Ivana") Add to list Journal Article A1 Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion Jelle van den Ameele (UGent) , Ivana Jedlickova, Anna Pristoupilova, Anne Sieben (UGent) , Sara Van Mossevelde, Chantal Ceuterick-de Groote, Helena Hůlková, Radoslav Matej, Alfred Meurs, Christine Van Broeckhoven, et al. (2018) NEUROLOGY. 90(8). p.e658-e663 Add to list Journal Article A1 open access Heterozygous loss-of-function SEC61A1 mutations cause autosomal-dominant tubulo-interstitial and glomerulocystic kidney disease with anemia Nikhita Ajit Bolar, Christelle Golzio, Martina Živná, Gaëlle Hayot, CHRISTINE VAN HEMELRIJK (UGent) , Dorien Schepers, Geert Vandeweyer, Alexander Hoischen, Jeroen R Huyghe, Ann Raes (UGent) , et al. (2016) AMERICAN JOURNAL OF HUMAN GENETICS. 99(1). p.174-187