Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Save this search Download search results Subscribe to news feed Your filters: cql: author="Schrooten, Maarten" or (type any "bookEditor issueEditor" and editor="Schrooten, Maarten") Add to list Journal Article A2 Negative commercial screening test for paraneoplastic antibodies in a case of opsoclonus Nicolas Vandenbussche (UGent) , Catherine Cassiman, Maarten Schrooten, Benjamin Gille, Xavier Bossuyt, Thierry Vincent, Philip Van Damme and Koen Poesen (2017) NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION. 4(2). Add to list Journal Article A1 Mutations in PEX10 are a cause of autosomal recessive ataxia Luc Régal, Merel S Ebberink, Nathalie Goemans, Ronald JA Wanders, Linda De Meirleir, Jacques Jaeken, Maarten Schrooten, Rudy Van Coster (UGent) and Hans R Waterham (2010) ANNALS OF NEUROLOGY. 68(2). p.259-263 Add to list Conference Paper C3 Mutations in PEX10 Are a Cause of Autosomal Recessive Spinocerebellar Ataxia Luc Régal, Merel Ebberink, Ronald Wanders, Hans Waterham, Linda De Meirleir, Jaak Jaeken, Rudy Van Coster (UGent) , Maarten Schrooten and Nathalie Goemans (2009) Neurology. 72(11). p.A396-A396