The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter von Gijselinck, I, Van Mossevelde, S, van der Zee, J, Sieben, A, Engelborghs, S, De Bleecker, J, Ivanoiu, A, Deryck, O, Edbauer, D, Zhang, M, Heeman, B, Bäumer, V, Van den Broeck, M, Mattheijssens, M, Peeters, K, Rogaeva, E, De Jonghe, P, Cras, P, Martin, J-J, de Deyn, P P, Cruts, M, Van Broeckhoven, C

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Mild Cognitive Impairment: Differential Atrophy in the Hippocampal Subfields von HANSEEUW, B. J, VAN LEEMPUT, K, KAVEC, M, GRANDIN, C, SERON, X, IVANOIU, A

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Case of Susac's syndrome initially diagnosed as multiple sclerosis von Hemptinne, C., Boschi, A., Duprez, T., Ivanoiu, A., Coutel, M.

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How does Parkinson’s disease and aging affect temporal expectation and the implicit timing of eye movements? von de Hemptinne, C., Ivanoiu, A., Lefèvre, P., Missal, M.

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Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia von Cuyvers, Elise, Bettens, Karolien, Philtjens, Stéphanie, Van Langenhove, Tim, Gijselinck, Ilse, van der Zee, Julie, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu, Van Dongen, Jasper, Geerts, Nathalie, Maes, Githa, Mattheijssens, Maria, Peeters, Karin, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter P, Van Broeckhoven, Christine, Cruts, Marc, Sleegers, Kristel

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Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort von Gijselinck, Ilse, Van Mossevelde, Sara, van der Zee, Julie, Sieben, Anne, Philtjens, Stéphanie, Heeman, Bavo, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu, De Baets, Greet, Bäumer, Veerle, Cuijt, Ivy, Van den Broeck, Marleen, Peeters, Karin, Mattheijssens, Maria, Rousseau, Frederic, Vandenberghe, Rik, De Jonghe, Peter, Cras, Patrick, De Deyn, Peter P, Martin, Jean-Jacques, Cruts, Marc, Van Broeckhoven, Christine

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Improved discrimination of AD patients using β-amyloid(1-42) and tau levels in CSF von HULSTAERT, F, BLENNOW, K, IQBAL, K, POTTEL, H, VANMECHELEN, E, VANDERSTICHELE, H, IVANOIU, A, SCHOONDERWALDT, H. C, RIEMENSCHNEIDER, M, DE DEYN, P. P, BANCHER, C, CRAS, P, WILTFANG, J, MEHTA, P. D

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Bilateral brachial plexopathy as the presenting symptom of giant cell arteritis von London, F., Pothen, L., Lambert, M., Ivanoiu, A.

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Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort von Van Mossevelde, Sara, van der Zee, Julie, Gijselinck, Ilse, Engelborghs, Sebastiaan, Sieben, Anne, Van Langenhove, Tim, De Bleecker, Jan, Baets, Jonathan, Vandenbulcke, Mathieu, Van Laere, Koen, Ceyssens, Sarah, Van den Broeck, Marleen, Peeters, Karin, Mattheijssens, Maria, Cras, Patrick, Vandenberghe, Rik, De Jonghe, Peter, Martin, Jean-Jacques, De Deyn, Peter P, Cruts, Marc, Van Broeckhoven, Christine

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Progress in the Treatment of Alzheimer’s Disease Is Needed – Position Statement of European Alzheimer’s Disease Consortium (EADC) Investigators von Jessen, Frank, Kramberger, M. G., Angioni, D., Aarsland, D., Balasa, M., Bennys, K., Boada, M., Boban, M., Chincarini, A., Exalto, L., Felbecker, A., Fliessbach, K., Frisoni, G. B., Garza-Martínez, A. J., Grimmer, T., Hanseeuw, B., Hort, J., Ivanoiu, A., Klöppel, S., Krajcovicova, L., McGuinness, B., Mecocci, P., de Mendonca, A., Nous, A., Ousset, P.-J., Paquet, C., Perneczky, R., Peters, O., Tabuas-Pereira, M., Piazza, F., Plantone, D., Riverol, M., Ruiz, A., Sacco, G., Santana, I., Scarmeas, N., Solje, E., Stefanova, E., Sutovsky, S., van der Flier, W., Welsh, T., Wimo, A., Winblad, B., Frölich, L., Engelborghs, S.

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Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients von Perrone, Federica, Nguyen, Hung Phuoc, Van Mossevelde, Sara, Moisse, Matthieu, Sieben, Anne, Santens, Patrick, De Bleecker, Jan, Vandenbulcke, Mathieu, Engelborghs, Sebastiaan, Baets, Jonathan, Cras, Patrick, Vandenberghe, Rik, De Jonghe, Peter, De Deyn, Peter P, Martin, Jean-Jacques, Van Damme, Philip, Van Broeckhoven, Christine, van der Zee, Julie

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An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer’s disease von De Roeck, Arne, Duchateau, Lena, Van Dongen, Jasper, Cacace, Rita, Bjerke, Maria, Van den Bossche, Tobi, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter P., Engelborghs, Sebastiaan, Van Broeckhoven, Christine, Sleegers, Kristel

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NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients von Nguyen, Hung Phuoc, Van Mossevelde, Sara, Dillen, Lubina, De Bleecker, Jan L., Moisse, Matthieu, Van Damme, Philip, Van Broeckhoven, Christine, van der Zee, Julie, Engelborghs, Sebastiaan, Crols, Roeland, De Deyn, Peter P., De Jonghe, Peter, Baets, Jonathan, Cras, Patrick, Mercelis, Rudy, Vandenberghe, Rik, Sieben, Anne, Santens, Patrick, Ivanoiu, Adrian, Deryck, Olivier, Vanopdenbosch, Ludo, Delbeck, Jean

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Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability von Cacace, Rita, Heeman, Bavo, Van Mossevelde, Sara, De Roeck, Arne, Hoogmartens, Julie, De Rijk, Peter, Gossye, Helena, De Vos, Kristof, De Coster, Wouter, Strazisar, Mojca, De Baets, Greet, Schymkowitz, Joost, Rousseau, Frederic, Geerts, Nathalie, De Pooter, Tim, Peeters, Karin, Sieben, Anne, Martin, Jean-Jacques, Engelborghs, Sebastiaan, Salmon, Eric, Santens, Patrick, Vandenberghe, Rik, Cras, Patrick, P. De Deyn, Peter, C. van Swieten, John, M. van Duijn, Cornelia, van der Zee, Julie, Sleegers, Kristel, Van Broeckhoven, Christine

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Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation von Van den Bossche, Tobi, Sleegers, Kristel, Cuyvers, Elise, Engelborghs, Sebastiaan, Sieben, Anne, De Roeck, Arne, Van Cauwenberghe, Caroline, Vermeulen, Steven, Van den Broeck, Marleen, Laureys, Annelies, Peeters, Karin, Mattheijssens, Maria, Vandenbulcke, Mathieu, Vandenberghe, Rik, Martin, Jean-Jacques, De Deyn, Peter P, Cras, Patrick, Van Broeckhoven, Christine

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Harmonizing neuropsychological assessment for mild neurocognitive disorders in Europe von Boccardi, Marina, Monsch, Andreas U., Ferrari, Clarissa, Altomare, Daniele, Berres, Manfred, Bos, Isabelle, Buchmann, Andreas, Cerami, Chiara, Didic, Mira, Festari, Cristina, Nicolosi, Valentina, Sacco, Leonardo, Aerts, Liesbeth, Albanese, Emiliano, Annoni, Jean‐Marie, Ballhausen, Nicola, Chicherio, Christian, Démonet, Jean‐François, Descloux, Virginie, Diener, Suzie, Ferreira, Daniel, Georges, Jean, Gietl, Anton, Girtler, Nicola, Kilimann, Ingo, Klöppel, Stefan, Kustyniuk, Nicole, Mecocci, Patrizia, Mella, Nathalie, Pigliautile, Martina, Seeher, Katrin, Shirk, Steven D., Toraldo, Alessio, Brioschi‐Guevara, Andrea, Chan, Kwun C. G., Crane, Paul K., Dodich, Alessandra, Grazia, Alice, Kochan, Nicole A, Oliveira, Fabricio Ferreira, Nobili, Flavio, Kukull, Walter, Peters, Oliver, Ramakers, Inez, Sachdev, Perminder S., Teipel, Stefan, Visser, Pieter Jelle, Wagner, Michael, Weintraub, Sandra, Westman, Eric, Froelich, Lutz, Brodaty, Henry, Dubois, Bruno, Cappa, Stefano F., Salmon, David, Winblad, Bengt, Frisoni, Giovanni B., Kliegel, Matthias

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Poliomyelitis-like syndrome with matching magnetic resonance features in a case of Lyme neuroborreliosis von Charles, V, Duprez, T P, Kabamba, B, Ivanoiu, A, Sindic, C J M

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No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients von Baradaran-Heravi, Yalda, Dillen, Lubina, Nguyen, Hung Phuoc, Van Mossevelde, Sara, Baets, Jonathan, De Jonghe, Peter, Engelborghs, Sebastiaan, De Deyn, Peter P., Vandenbulcke, Mathieu, Vandenberghe, Rik, Van Damme, Philip, Cras, Patrick, Salmon, Eric, Synofzik, Matthis, Heutink, Peter, Wilke, Carlo, Simon-Sanchez, Javier, Rojas-Garcia, Ricard, Turon-Sans, Janina, Lleó, Alberto, Illán-Gala, Ignacio, Clarimón, Jordi, Borroni, Barbara, Padovani, Alessandro, Pastor, Pau, Diez-Fairen, Monica, Aguilar, Miquel, Gelpi, Ellen, Sanchez-Valle, Raquel, Borrego-Ecija, Sergi, Matej, Radoslav, Parobkova, Eva, Nacmias, Benedetta, Sorbi, Sandro, Bagnoli, Silvia, de Mendonça, Alexandre, Ferreira, Catarina, Fraidakis, Matthew J., Diehl-Schmid, Janine, Alexopoulos, Panagiotis, Almeida, Maria Rosário, Santana, Isabel, Van Broeckhoven, Christine, van der Zee, Julie, Goeman, Johan, Nuytten, Dirk, Sieben, Anne, De Bleecker, Jan L., Santens, Patrick, Versijpt, Jan, Michotte, Alex, Ivanoiu, Adrian, Deryck, Olivier, Bergmans, Bruno, Willems, Christiana, De Klippel, Nina, Peeters, Dirk, Archettim, Silvana, Bonomi, Elisa, Piaceri, Irene, Ferrari, Camilla, Simões do Couto, Frederico, Verdelho, Ana, Miltenberger-Miltényi, Gabriel

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Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort von Verheijen, Jan, van der Zee, Julie, Gijselinck, Ilse, Van den Bossche, Tobi, Dillen, Lubina, Heeman, Bavo, Gómez-Tortosa, Estrella, Lladó, Albert, Sanchez-Valle, Raquel, Graff, Caroline, Pastor, Pau, Pastor, Maria A., Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Clarimon, Jordi, de Mendonça, Alexandre, Gelpi, Ellen, Tsolaki, Magda, Diehl-Schmid, Janine, Nacmias, Benedetta, Almeida, Maria Rosário, Borroni, Barbara, Matej, Radoslav, Ruiz, Agustín, Engelborghs, Sebastiaan, Vandenberghe, Rik, De Deyn, Peter P., Cruts, Marc, Van Broeckhoven, Christine, Sleegers, Kristel, Goeman, Johan, Nuytten, Dirk, Vandenbulcke, Mathieu, Santens, Patrick, De Bleecker, Jan, Sieben, Anne, Dermaut, Bart, Versijpt, Jan, Michotte, Alex, Deryck, Olivier, Bergmans, Bruno, Willems, Christiana, Ivanoiu, Adrian, Salmon, Eric, Alexopoulos, Panagiotis, Sorbi, Sandro, Bessi, Valentina, Bagnoli, Silvia, Santana, Isabel, Simões do Couto, Frederico, Martins, Madalena, Thonberg, Håkan, Fratiglioni, Laura, Padovani, Alessandro, Rohan, Zdenek, Razquin, Cristina, Lorenzo, Elena, Iglesias, Elena, Seijo-Martínez, Manuel, Rene, Ramon, Gascon, Jordi, Campdelacreu, Jaume, Koutroumani, Maria, Lleó, Alberto, Fortea, Juan, Blesa, Rafael

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Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients von Dillen, Lubina, Van Langenhove, Tim, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu, Sarafov, Stayko, Tournev, Ivailo, Merlin, Celine, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter P, Jordanova, Albena, Cruts, Marc, Van Broeckhoven, Christine, van der Zee, Julie

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