Relationship between C9orf72 repeat size and clinical phenotype von Van Mossevelde, Sara, van der Zee, Julie, Cruts, Marc, Van Broeckhoven, Christine

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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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Genotype–phenotype links in frontotemporal lobar degeneration von Van Mossevelde, Sara, Engelborghs, Sebastiaan, van der Zee, Julie, Van Broeckhoven, Christine

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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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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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Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration von Goossens, Joery, Bjerke, Maria, Van Mossevelde, Sara, Van den Bossche, Tobi, Goeman, Johan, De Vil, Bart, Sieben, Anne, Martin, Jean-Jacques, Cras, Patrick, De Deyn, Peter Paul, Van Broeckhoven, Christine, van der Zee, Julie, Engelborghs, Sebastiaan

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Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease von 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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No added diagnostic value of non-phosphorylated tau fraction (p-tau rel ) in CSF as a biomarker for differential dementia diagnosis von Goossens, Joery, Bjerke, Maria, Struyfs, Hanne, Niemantsverdriet, Ellis, Somers, Charisse, Van den Bossche, Tobi, Van Mossevelde, Sara, De Vil, Bart, Sieben, Anne, Martin, Jean-Jacques, Cras, Patrick, Goeman, Johan, De Deyn, Peter Paul, Van Broeckhoven, Christine, van der Zee, Julie, Engelborghs, Sebastiaan

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Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family von Sieben, Anne, Van Mossevelde, Sara, Wauters, Eline, Engelborghs, Sebastiaan, van der Zee, Julie, Van Langenhove, Tim, Santens, Patrick, Praet, Marleen, Boon, Paul, Miatton, Marijke, Van Hoecke, Sofie, Vandenbulcke, Mathieu, Vandenberghe, Rik, Cras, Patrick, Cruts, Marc, De Deyn, Peter Paul, Van Broeckhoven, Christine, Martin, Jean-Jacques

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Association of short-term cognitive decline and MCI-to-AD dementia conversion with CSF, MRI, amyloid- and 18F-FDG-PET imaging von Ottoy, Julie, Niemantsverdriet, Ellis, Verhaeghe, Jeroen, De Roeck, Ellen, Struyfs, Hanne, Somers, Charisse, wyffels, Leonie, Ceyssens, Sarah, Van Mossevelde, Sara, Van den Bossche, Tobi, Van Broeckhoven, Christine, Ribbens, Annemie, Bjerke, Maria, Stroobants, Sigrid, Engelborghs, Sebastiaan, Staelens, Steven

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Tacrolimus-induced cognitive impairment: a case report von Deprez, Valerie, Goeman, Johan, Van Mossevelde, Sara

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Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains von 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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Modifiers of GRN-Associated Frontotemporal Lobar Degeneration von Wauters, Eline, Van Mossevelde, Sara, Van der Zee, Julie, Cruts, Marc, Van Broeckhoven, Christine

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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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Prevalence and Phenotype of TBK1 Mutations: an In-Depth Description (P11-3.001) von Gossye, Helena, Van Mossevelde, Sara, De Bleecker, Jan, Cras, Patrick, Engelborghs, Sebastiaan, De Deyn, Peter, Van Langenhove, Tim, Van Broeckhoven, Christine

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Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum von Gossye, Helena, Van Mossevelde, Sara, Sieben, Anne, Bjerke, Maria, Hendrickx Van de Craen, Elisabeth, van der Zee, Julie, De Deyn, Peter P, De Bleecker, Jan, Versijpt, Jan, van den Ende, Jenneke, Deryck, Olivier, Bourgeois, Paul, Bier, Jean-Christophe, Goethals, Maarten, Vandenberghe, Rik, Engelborghs, Sebastiaan, Van Broeckhoven, Christine

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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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Frequent MAPT p.R406W Carriers with a Nonconforming FTD Phenotype in the Belgian Population (S20.006) von Gossye, Helena, Van Mossevelde, Sara, Van Der Zee, Julie, Sieben, Anne, Bjerke, Maria, Engelborghs, Sebastiaan, De Deyn, Peter, De Bleecker, Jan, Versijpt, Jan, Van Den Ende, Jenneke, Deryck, Olivier, Bourgeois, Paul, Bier, Jean-Christophe, Goethals, Maarten, Van Broeckhoven, Christine

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Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion von Van Mossevelde, Sara, van der Zee, Julie, Gijselinck, Ilse, Sleegers, Kristel, De Bleecker, Jan, Sieben, Anne, Vandenberghe, Rik, Van Langenhove, Tim, Baets, Jonathan, Deryck, Olivier, Santens, Patrick, Ivanoiu, Adrian, Willems, Christiana, Bäumer, Veerle, Van den Broeck, Marleen, Peeters, Karin, Mattheijssens, Maria, De Jonghe, Peter, Cras, Patrick, Martin, Jean-Jacques, Cruts, Marc, De Deyn, Peter P, Engelborghs, Sebastiaan, Van Broeckhoven, Christine

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Genetic screening in early-onset dementia patients with unclear phenotype: relevance for clinical diagnosis von Perrone, Federica, Cacace, Rita, Van Mossevelde, Sara, Van den Bossche, Tobi, De Deyn, Peter P., Cras, Patrick, Engelborghs, Sebastiaan, van der Zee, Julie, Van Broeckhoven, Christine

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