Show 50 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="Perrone, Federica*" or (type exact bookEditor and editor="Perrone, Federica*") Add to list Journal Article A1 open access Amyloid-β1–43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations Federica Perrone, Maria Bjerke, Elisabeth Hens, Anne Sieben (UGent) , Maarten Timmers, Arne De Roeck, Rik Vandenberghe, Kristel Sleegers, Jean-Jacques Martin, Peter P. De Deyn, et al. (2020) ALZHEIMERS RESEARCH & THERAPY. 12(1). Add to list Journal Article A1 open access TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, Federica Perrone, Lubina Dillen, Bavo Heeman, Veerle Bäumer, Sebastiaan Engelborghs, Jan De Bleecker (UGent) , Jonathan Baets, et al. (2017) HUMAN MUTATION. 38(3). p.297-309 Add to list Journal Article A1 Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients Federica Perrone, Hung Phuoc Nguyen, Sara Van Mossevelde, Matthieu Moisse, Anne Sieben (UGent) , Patrick Santens (UGent) , Jan De Bleecker (UGent) , Mathieu Vandenbulcke, Sebastiaan Engelborghs, Jonathan Baets, et al. (2017) NEUROBIOLOGY OF AGING. 51. p.177.e9-177.e16 Add to list Journal Article A2 open access Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD Julie van der Zee, Peter Marien, Roeland Crols, Sara Van Mossevelde, Lubina Dillen, Federica Perrone, Sebastiaan Engelborghs, Jo Verhoeven, Tine D'aes, Chantal Ceuterick-De Groote, et al. (2016) NEUROLOGY-GENETICS. 2(5).