Mutations in ABCA7 in a Belgian cohort of Alzheimer's disease patients: a targeted resequencing study von Cuyvers, Elise, MSc, De Roeck, Arne, MSc, Van den Bossche, Tobi, MD, Van Cauwenberghe, Caroline, MSc, Bettens, Karolien, PhD, Vermeulen, Steven, MSc, Mattheijssens, Maria, BSc, Peeters, Karin, BSc, Engelborghs, Sebastiaan, Prof, Vandenbulcke, Mathieu, Prof, Vandenberghe, Rik, Prof, De Deyn, Peter P, Prof, Van Broeckhoven, Christine, Prof, Sleegers, Kristel, Prof

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A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer’s disease von Verheijen, Jan, Van den Bossche, Tobi, van der Zee, Julie, Engelborghs, Sebastiaan, Sanchez-Valle, Raquel, Lladó, Albert, Graff, Caroline, Thonberg, Håkan, Pastor, Pau, Ortega-Cubero, Sara, Pastor, Maria A., Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Clarimon, Jordi, Lleó, Alberto, Fortea, Juan, de Mendonça, Alexandre, Martins, Madalena, Grau-Rivera, Oriol, Gelpi, Ellen, Bettens, Karolien, Mateiu, Ligia, Dillen, Lubina, Cras, Patrick, De Deyn, Peter P., Van Broeckhoven, Christine, Sleegers, Kristel

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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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O4‐01‐01: IN‐DEPTH ANALYSIS OF AN ABCA7 VNTR IN ALZHEIMER'S DISEASE von De Roeck, Arne, Duchateau, Lena, Van Dongen, Jasper, Cacace, Rita, Bjerke, Maria, Bossche, Tobi, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter Paul, Engelborghs, Sebastiaan, Van Broeckhoven, Christine, Sleegers, Kristel

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P3‐128: EXPLORING THE MOLECULAR MECHANISM OF NEURONAL HYPEREXCITABILITY IN DEMENTIA von Cacace, Rita, Hoogmartens, Julie, Van Mossevelde, Sara, Bossche, Tobi, Geerts, Nathalie, Vandenberghe, Rik, De Deyn, Peter Paul, Zee, Julie, Engelborghs, Sebastiaan, Sleegers, Kristel, Van Broeckhoven, Christine

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Myoclonus and Cerebellar Ataxia Following COVID‐19 von Dijkstra, Femke, Van den Bossche, Tobi, Willekens, Barbara, Cras, Patrick, Crosiers, David

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Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort von Cacace, Rita, Van den Bossche, Tobi, Engelborghs, Sebastiaan, Geerts, Nathalie, Laureys, Annelies, Dillen, Lubina, Graff, Caroline, Thonberg, Håkan, Chiang, Huei-Hsin, Pastor, Pau, Ortega-Cubero, Sara, Pastor, Maria A., Diehl-Schmid, Janine, Alexopoulos, Panagiotis, Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Nacmias, Benedetta, Sorbi, Sandro, Sanchez-Valle, Raquel, Lladó, Albert, Gelpi, Ellen, Almeida, Maria Rosário, Santana, Isabel, Tsolaki, Magda, Koutroumani, Maria, Clarimon, Jordi, Lleó, Alberto, Fortea, Juan, de Mendonça, Alexandre, Martins, Madalena, Borroni, Barbara, Padovani, Alessandro, Matej, Radoslav, Rohan, Zdenek, Vandenbulcke, Mathieu, Vandenberghe, Rik, De Deyn, Peter P., Cras, Patrick, van der Zee, Julie, Sleegers, Kristel, Van Broeckhoven, Christine

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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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P3‐017: Rare variants in PLD3 do not increase risk in a belgian cohort of early‐onset Alzheimer dementia patients von Cacace, Rita, Bossche, Tobi, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu, Vandenberghe, Rik, Deyn, Peter P., Cras, Patrick, Sleegers, Kristel, Broeckhoven, Christine

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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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P4‐194: The identification of high‐penetrant loss‐of‐function mutations in abca7 in Alzheimer's disease von Cuyvers, Elise, Roeck, Arne, Bossche, Tobi, Cauwenberghe, Caroline, Bettens, Karolien, Vermeulen, Steven, Mattheijssens, Maria, Peeters, Karin, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu, Vandenberghe, Rik, Deyn, Peter P., Broeckhoven, Christine, Sleegers, Kristel

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Early-onset dementia in a middle-aged female: a case reflecting the compromise between pragmatic treatment of mimickers and extensive diagnostics von Vivier, Yann, Van den Bossche, Tobi, Loos, Caroline

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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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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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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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The extended Belgian presenilin 1 Alzheimer family AD/A revisited. (P1.092) von Van den Bossche, Tobi, De Deyn, Peter P, Martin, Jean-Jacques, Cras, Patrick, Van Broeckhoven, Christine

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Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease von De Roeck, Arne, Van den Bossche, Tobi, van der Zee, Julie, Verheijen, Jan, De Coster, Wouter, Van Dongen, Jasper, Dillen, Lubina, Baradaran-Heravi, Yalda, Heeman, Bavo, Sanchez-Valle, Raquel, Lladó, Albert, Nacmias, Benedetta, Sorbi, Sandro, Gelpi, Ellen, Grau-Rivera, Oriol, Gómez-Tortosa, Estrella, Pastor, Pau, Ortega-Cubero, Sara, Pastor, Maria A., Graff, Caroline, Thonberg, Håkan, Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, de Mendonça, Alexandre, Martins, Madalena, Borroni, Barbara, Padovani, Alessandro, Almeida, Maria Rosário, Santana, Isabel, Diehl-Schmid, Janine, Alexopoulos, Panagiotis, Clarimon, Jordi, Lleó, Alberto, Fortea, Juan, Tsolaki, Magda, Koutroumani, Maria, Matěj, Radoslav, Rohan, Zdenek, De Deyn, Peter, Engelborghs, Sebastiaan, Cras, Patrick, Van Broeckhoven, Christine, Sleegers, Kristel

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In a Large Belgian AD Cohort Loss of ABCA7 Mutations Are Associated with Alzheimer’s Disease and Cerebral Amyloid Angiopathy. (1779) von Hens, Elisabeth, Bossaerts, Liene, Van den Bossche, Tobi, Engelborghs, Sebastiaan, Peeters, Karin, Van den Broeck, Marleen, Vermeiren, Yannick, Laureys, Annelies, De Roeck, Naomi, Hanseeuw, Bernard, Sieben, Anne, Vandenberghe, Rik, Martin, Jean-Jacques, De Deyn, Peter, Cras, Patrick, Van Broeckhoven, Christine

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ABCA7 mutations are major contributors to Alzheimer’s disease in Belgian patients: Genetics/genetic factors of Alzheimer's disease von Bossaerts, Liene, Hens, Elisabeth, Van den Bossche, Tobi, De Roeck, Arne, Engelborghs, Sebastiaan, Peeters, Karin, De Deyn, Peter Paul, Sleegers, Kristel, Van Broeckhoven, Christine

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ABCA7 mutations are major contributors to Alzheimer’s disease in Belgian patients von Bossaerts, Liene, Hens, Elisabeth, Van den Bossche, Tobi, De Roeck, Arne, Engelborghs, Sebastiaan, Peeters, Karin, De Deyn, Peter Paul, Sleegers, Kristel, Van Broeckhoven, Christine

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