γ-secretases: from cell biology to therapeutic strategies by Bergmans, Bruno A, MD, De Strooper, Bart, MD

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Defective membrane expression of the Na⁺-HCO₃⁻ cotransporter NBCe1 is associated with familial migraine by Suzuki, Masashi, Van Paesschen, Wim, Stalmans, Ingeborg, Horita, Shoko, Yamada, Hideomi, Bergmans, Bruno A, Legius, Eric, Riant, Florence, De Jonghe, Peter, Li, Yuehong, Sekine, Takashi, Igarashi, Takashi, Fujimoto, Ichiro, Mikoshiba, Katsuhiko, Shimadzu, Mitsunobu, Shiohara, Masaaki, Braverman, Nancy, Al-Gazali, Lihadh, Fujita, Toshiro, Seki, George

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Mutated ATP10B increases Parkinson’s disease risk by compromising lysosomal glucosylceramide export by Martin, Shaun, Smolders, Stefanie, Van den Haute, Chris, Heeman, Bavo, van Veen, Sarah, Crosiers, David, Beletchi, Igor, Verstraeten, Aline, Gossye, Helena, Gelders, Géraldine, Pals, Philippe, Hamouda, Norin Nabil, Engelborghs, Sebastiaan, Martin, Jean-Jacques, Eggermont, Jan, De Deyn, Peter Paul, Cras, Patrick, Baekelandt, Veerle, Vangheluwe, Peter, Van Broeckhoven, Christine

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Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease by Smolders, Stefanie, Philtjens, Stéphanie, Crosiers, David, Sieben, Anne, Hens, Elisabeth, Heeman, Bavo, Van Mossevelde, Sara, Pals, Philippe, Asselbergh, Bob, Dos Santos Dias, Roberto, Vermeiren, Yannick, Vandenberghe, Rik, Engelborghs, Sebastiaan, De Deyn, Peter Paul, Martin, Jean-Jacques, Cras, Patrick, Annaert, Wim, Van Broeckhoven, Christine

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Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort by 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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Neurons Generated from APP/APLP1/APLP2 Triple Knockout Embryonic Stem Cells Behave Normally in Vitro and in Vivo: Lack of Evidence for a Cell Autonomous Role of the Amyloid Precurs... by Bergmans, Bruno A., Shariati, S. Ali M., Habets, Ron L.P., Verstreken, Patrik, Schoonjans, Luc, Müller, Ulrike, Dotti, Carlos G., De Strooper, Bart

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Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients by 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 by 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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Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability by 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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Clinical variability and onset age modifiers in an extended Belgian GRN founder family by Wauters, Eline, Van Mossevelde, Sara, Sleegers, Kristel, van der Zee, Julie, Engelborghs, Sebastiaan, Sieben, Anne, Vandenberghe, Rik, Philtjens, Stéphanie, Van den Broeck, Marleen, Peeters, Karin, Cuijt, Ivy, De Coster, Wouter, Van Langenhove, Tim, Santens, Patrick, Ivanoiu, Adrian, Cras, Patrick, De Bleecker, Jan L., Versijpt, Jan, Crols, Roeland, De Klippel, Nina, Martin, Jean-Jacques, De Deyn, Peter P., Cruts, Marc, Van Broeckhoven, Christine, Goeman, Johan, Nuytten, Dirk, Vandenbulcke, Mathieu, Michotte, Alex, Salmon, Eric, Deryck, Olivier, Bergmans, Bruno, Willems, Christiana, Delbeck, Jean

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Levodopa-carbidopa intestinal gel in advanced Parkinson's: Final results of the GLORIA registry by Antonini, Angelo, Poewe, Werner, Chaudhuri, K. Ray, Jech, Robert, Pickut, Barbara, Pirtošek, Zvezdan, Szasz, Jozsef, Valldeoriola, Francesc, Winkler, Christian, Bergmann, Lars, Yegin, Ashley, Onuk, Koray, Barch, David, Odin, Per, Amalia, Ene, Arnold, Guy, Bajenaru, Ovidiu, Bergmans, Bruno, Bjornara, Kari Anne, Blackie, Jeff, Bode, Matthias, Bourgeois, Paul, Bohlhalter, Stephan, Buraga, Ioan, Burkhard, Pierre R., Busson, Philippe, Calopa, Matilde, Clausen, Jesper, Danielsen, Erik Hvid, Defebvre, Luc, Delvaux, Valerie, Dethy, Sophie, Dietrichs, Espen, De Fabregues, Oriol, Gerhard, Ransmayr, Gusmaroli, Graziano, Hahn, Kirsten, Hauptmann, Björn, Henriksen, Tove, Hernandez-Vara, Jorge, Jeanjean, A., Kaiserova, Michaela, Kassubek, Jan, Kimber, Thomas, Konitsiotis, Spyridon, Krüger, Rejko, Kulisevsky, Jaime, Leenders, Jo, Lundqvist, Christofer, Ory Magne, F., Marano, Pietro, Milanov, Ivan, Modugno, Nicola, Misbahuddin, Anjum, Nevrly, Martin, Panayiotis, Zikos, Pedersen, Kenn Freddy, Pedersen, Stephen W., Perju-Dumbrava, Lacramioara, Ponsen, M.M., Popescu, Bogdan O., Rijntjes, Michel, Puente, V., Redecker, Christoph, Schrader, Christoph, Sensi, Mariachiara, Simu, Mihaela, Spanaki, Cleanthe, Storch, Alexander, Storstein, Anette, Tomantschger, Volker, van der Linden, Chris, van Laar, T., Viallet, F., Witjas, Tatiana, Wolz, Martin, Zibetti, Maurizio, Van Zandijcke, Michel

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No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients by 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 by 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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Amyloid-β 1-43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations by Perrone, Federica, Bjerke, Maria, Hens, Elisabeth, Sieben, Anne, Timmers, Maarten, De Roeck, Arne, Vandenberghe, Rik, Sleegers, Kristel, Martin, Jean-Jacques, De Deyn, Peter P, Engelborghs, Sebastiaan, van der Zee, Julie, Van Broeckhoven, Christine, Cacace, Rita

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Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains by Janssens, Jonathan, Philtjens, Stéphanie, Kleinberger, Gernot, Van Mossevelde, Sara, van der Zee, Julie, Cacace, Rita, Engelborghs, Sebastiaan, Sieben, Anne, Banzhaf-Strathmann, Julia, Dillen, Lubina, Merlin, Céline, Cuijt, Ivy, Robberecht, Caroline, Schmid, Bettina, Santens, Patrick, Ivanoiu, Adrian, Vandenbulcke, Mathieu, Vandenberghe, Rik, Cras, Patrick, De Deyn, Peter P, Martin, Jean-Jacques, Maudsley, Stuart, Haass, Christian, Cruts, Marc, Van Broeckhoven, Christine

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23. Predictive parameters for the effect of botulinum neurotoxin infiltrations in chronic migraine by Bergmans, Bruno A., Bruffaerts, R., Verhalle, M., Vanopdenbosch, L., Verhoeven, K., Van Dycke, A., Deryck, O.

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[gamma]-secretases: from cell biology to therapeutic strategies by Bergmans, Bruno A, De Strooper, Bart

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Defective membrane expression of the Na + -HCO 3 − cotransporter NBCe1 is associated with familial migraine by Suzuki, Masashi, Van Paesschen, Wim, Stalmans, Ingeborg, Horita, Shoko, Yamada, Hideomi, Bergmans, Bruno A., Legius, Eric, Riant, Florence, De Jonghe, Peter, Li, Yuehong, Sekine, Takashi, Igarashi, Takashi, Fujimoto, Ichiro, Mikoshiba, Katsuhiko, Shimadzu, Mitsunobu, Shiohara, Masaaki, Braverman, Nancy, Al-Gazali, Lihadh, Fujita, Toshiro, Seki, George

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Defective membrane expression of the Na+-HCO^sub 3^- cotransporter NBCe1 is associated with familial migraine by Suzuki, Masashi, Van Paesschen, Wim, Stalmans, Ingeborg, Horita, Shoko, Yamada, Hideomi, Bergmans, Bruno A, Legius, Eric, Riant, Florence, De Jonghe, Peter, Li, Yuehong, Sekine, Takashi, Igarashi, Takashi, Fujimoto, Ichiro, Mikoshiba, Katsuhiko, Shimadzu, Mitsunobu, Shiohara, Masaaki, Braverman, Nancy, Al-Gazali, Lihadh, Fujita, Toshiro, Seki, George

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Defective membrane expression of the Na(+)-HCO(3)(-) cotransporter NBCe1 is associated with familial migraine by Suzuki, Masashi, Van Paesschen, Wim, Stalmans, Ingeborg, Horita, Shoko, Yamada, Hideomi, Bergmans, Bruno A, Legius, Eric, Riant, Florence, De Jonghe, Peter, Li, Yuehong, Sekine, Takashi, Igarashi, Takashi, Fujimoto, Ichiro, Mikoshiba, Katsuhiko, Shimadzu, Mitsunobu, Shiohara, Masaaki, Braverman, Nancy, Al-Gazali, Lihadh, Fujita, Toshiro, Seki, George

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