A global synthesis of the effectiveness of sedimentation-enhancing strategies for river deltas and estuaries von Cox, Jana R., Paauw, Mandy, Nienhuis, Jaap H., Dunn, Frances E., van der Deijl, Eveline, Esposito, Christopher, Goichot, Marc, Leuven, Jasper R.F.W., van Maren, Dirk S., Middelkoop, Hans, Naffaa, Safaa, Rahman, Munsur, Schwarz, Christian, Sieben, Eline, Triyanti, Annisa, Yuill, Brendan

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A global synthesis of the effectiveness of sedimentation-enhancing strategies for river deltas and estuaries von Cox, Jana R, Paauw, Mandy, Nienhuis, Jaap H, Dunn, Frances E, van der Deijl, Eveline, Esposito, Christopher, Goichot, Marc, Leuven, Jasper R.F.W, van Maren, Dirk S, Middelkoop, Hans, Naffaa, Safaa, Rahman, Munsur, Schwarz, Christian, Sieben, Eline, Triyanti, Annisa, Yuill, Brendan

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A global synthesis of the effectiveness of sedimentation-enhancing strategies for river deltas and estuaries von Cox, Jana R, Paauw, Mandy, Nienhuis, Jaap H, Dunn, Frances E, van der Deijl, Eveline, Esposito, Christopher, Goichot, Marc, Leuven, Jasper R.F.W, van Maren, Dirk S, Middelkoop, Hans, Naffaa, Safaa, Rahman, Munsur, Schwarz, Christian, Sieben, Eline, Triyanti, Annisa, Yuill, Brendan

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Sustainable floods: Exploring stakeholder perceptions of sedimentation strategies for the sinking Mekong delta von Dunn, Frances, Quee, Niki, Luu, Tang, Phuong, Gian Tang, Triyanti, Annisa, Du, Haomiao, Wyatt, Andrew, Sieben, Eline

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Neurogranin as biomarker in CSF is non-specific to Alzheimer's disease dementia von Willemse, Eline A.J., Sieben, Anne, Somers, Charisse, Vermeiren, Yannick, De Roeck, Naomi, Timmers, Maarten, Van Broeckhoven, Christine, De Vil, Bart, Cras, Patrick, De Deyn, Peter P., Martin, Jean-Jacques, Teunissen, Charlotte E., Engelborghs, Sebastiaan, Bjerke, Maria

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Rare exonic variant affects GRN splicing and contributes to frontotemporal lobar degeneration von Wauters, Eline, Gossye, Helena, Frydas, Alexandros, Sieben, Anne, Van Broeckhoven, Christine

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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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Clinical variability and onset age modifiers in an extended Belgian GRN founder family von 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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Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia von Philtjens, Stéphanie, Van Mossevelde, Sara, van der Zee, Julie, Wauters, Eline, Dillen, Lubina, Vandenbulcke, Mathieu, Vandenberghe, Rik, Ivanoiu, Adrian, Sieben, Anne, Willems, Christiana, Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Borroni, Barbara, Padovani, Alessandro, Pastor, Pau, Diez-Fairen, Monica, Aguilar, Miquel, de Mendonça, Alexandre, Miltenberger-Miltényi, Gabriel, Hernández, Isabel, Boada, Merce, Ruiz, Agustín, Nacmias, Benedetta, Sorbi, Sandro, Almeida, Maria Rosário, Santana, Isabel, Clarimón, Jordi, Lleó, Alberto, Frisoni, Giovanni B., Sanchez-Valle, Raquel, Lladó, Albert, Gómez-Tortosa, Estrella, Gelpi, Ellen, Van den Broeck, Marleen, Peeters, Karin, Cras, Patrick, De Deyn, Peter P., Engelborghs, Sebastiaan, Cruts, Marc, Van Broeckhoven, Christine

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Clinical variability and onset age modifiers in an extended Belgian GRN founder family von Wauters, Eline, Van Mossevelde, Sara, Sleegers, Kristel, van der Zee, Julie, Engelborghs, Sebastiaan, Sieben, Anne, Vandenberghe, Rik, Philtjens, Stephanie, 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

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Early intervention for cognitive decline von Eline, Dekens, Marijke, Miatton, Anne, Sieben, Patrick, Santens, Paul, Boon

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NEUROGRANIN IN CEREBROSPINAL FLUID IS NOT SPECIFIC TO ALZHEIMER’S DISEASE DEMENTIA von Willemse, Eline A.J., Sieben, Anne, Somers, Charisse, Vermeiren, Yannick, De Roeck, Naomi, Luyckx, Jill, Van Broeckhoven, Christine, De Vil, Bart, Cras, Patrick, De Deyn, Peter Paul, Martin, Jean-Jacques, Teunissen, Charlotte E., Engelborghs, Sebastiaan, Bjerke, Maria

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P4‐270: NEUROGRANIN IN CEREBROSPINAL FLUID IS NOT SPECIFIC TO ALZHEIMER'S DISEASE DEMENTIA von Willemse, Eline A.J., Sieben, Anne, Somers, Charisse, Vermeiren, Yannick, De Roeck, Naomi, Luyckx, Jill, Van Broeckhoven, Christine, De Vil, Bart, Cras, Patrick, De Deyn, Peter Paul, Martin, Jean-Jacques, Teunissen, Charlotte E., Engelborghs, Sebastiaan, Bjerke, Maria

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Clinical variability and onset age modifiers in an extended Belgian GRN founder family von Wauters, Eline, Van Mossevelde, Sara, Sleegers, Kristel, van der Zee, Julie, Engelborghs, Sebastiaan, Sieben, Anne, Vandenberghe, Rik, Philtjens, Stephanie, Van den Broeck, Marleen, Peeters, Karin, Cuijt, Ivy, De Coster, Wouter, Van Langenhove, Tim, Santens, Patrick, Ivanoiu, Adrian, Cras, Patrick, De Bleecker, Jan, Versijpt, Jan, Crols, Roeland, De Klippel, Nina, Martin, Jean-Jacques, De Deyn, Peter P, Cruts, Marc, Van Broeckhoven, Christine

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Comprehensive phenotypic description of the Belgian GRN founder family and genetic onset age modifiers (P1.085) von Van Mossevelde, Sara, Wauters, Eline, Sieben, Anne, Sleegers, Kristel, Gijselinck, Ilse, Philtjens, Stéphanie, Van Langenhove, Tim, Vandenbulcke, Mathieu, Cras, Patrick, Santens, Patrick, De Bleecker, Jan, Vandenberghe, Rik, Ivanoiu, Adrian, Versijpt, Jan, Crols, Roeland, De Deyn, Peter P., van der Zee, Julie, Cruts, Marc, Engelborghs, Sebastiaan, Van Broeckhoven, Christine

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Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia von Philtjens, Stephanie, Van Mossevelde, Sara, van der Zee, Julie, Wauters, Eline, Dillen, Lubina, Vandenbulcke, Mathieu, Vandenberghe, Rik, Ivanoiu, Adrian, Sieben, Anne, Willems, Christiana, Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Borroni, Barbara, Padovani, Alessandro, Pastor, Pau, Diez-Fairen, Monica, Aguilar, Miquel, de Mendonca, Alexandre, Miltenberger-Miltenyi, Gabriel, Hernandez, Isabel, Boada, Merce, Ruiz, Agustin, Nacmias, Benedetta, Sorbi, Sandro, Almeida, Maria Rosario, Santana, Isabel, Clarimon, Jordi, Lleo, Alberto, Frisoni, Giovanni B, Sanchez-Valle, Raquel, Llado, Albert, Gomez-Tortosa, Estrella, Gelpi, Ellen, Van den Broeck, Marleen, Peeters, Karin, Cras, Patrick, De Deyn, Peter P, Engelborghs, Sebastiaan, Cruts, Marc, Van Broeckhoven, Christine

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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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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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Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia von Philtjens, Stéphanie, Van Mossevelde, Sara, Van der Zee, Julie, Wauters, Eline, Dillen, Lubina, Vandenbulcke, Mathieu, Vandenberghe, Rik, Ivanoiu, Adrian, Sieben, Anne, Willems, Christiana, Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Borroni, Barbara, Padovani, Alessandro, Pastor, Pau, Diez-Fairen, Monica, Aguilar, Miquel, de Mendonça, Alexandre, Miltenberger-Miltényi, Gabriel, Hernández, Isabel, Boada, Mercè, Ruiz, A, Nacmias, Benedetta, Sorbi, S, Almeida, M.Rosario, Santana, Isabel, Clarimón, Jordi, Lleó, Alberto, Frisoni, Giovanni B, Sanchez-Valle, Raquel, Llado Plarrumani, Albert, Gómez-Tortosa, Estrella, Gelpi, Ellen, Van den Broeck, Marleen, Peeters, Karin, Cras, Patrick, De Deyn, Peter Paul, Engelborghs, Sebastiaan, Cruts, Marc, Van Broeckhoven, Christine, Universitat Autònoma de Barcelona

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