A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identificati... von Gijselinck, Ilse, PhD, Van Langenhove, Tim, MD, van der Zee, Julie, PhD, Sleegers, Kristel, PhD, Philtjens, Stéphanie, MSc, Kleinberger, Gernot, MSc, Janssens, Jonathan, MSc, Bettens, Karolien, PhD, Van Cauwenberghe, Caroline, MSc, Pereson, Sandra, MSc, Engelborghs, Sebastiaan, Prof, Sieben, Anne, MD, De Jonghe, Peter, Prof, Vandenberghe, Rik, Prof, Santens, Patrick, Prof, De Bleecker, Jan, Prof, Maes, Githa, MSc, Bäumer, Veerle, BSc, Dillen, Lubina, PhD, Joris, Geert, BSc, Cuijt, Ivy, MSc, Corsmit, Ellen, BSc, Elinck, Ellen, MSc, Van Dongen, Jasper, BSc, Vermeulen, Steven, MSc, Van den Broeck, Marleen, BSc, Vaerenberg, Carolien, MSc, Mattheijssens, Maria, BSc, Peeters, Karin, BSc, Robberecht, Wim, Prof, Cras, Patrick, Prof, Martin, Jean-Jacques, Prof, De Deyn, Peter P, Prof, Cruts, Marc, Prof, Van Broeckhoven, Christine, Prof

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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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TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and Amyotrophic Lateral Sclerosis von van der Zee, Julie, Gijselinck, Ilse, Van Mossevelde, Sara, Perrone, Federica, Dillen, Lubina, Heeman, Bavo, Bäumer, Veerle, Engelborghs, Sebastiaan, De Bleecker, Jan, Baets, Jonathan, Gelpi, Ellen, Rojas-García, Ricardo, Clarimón, Jordi, Lleó, Alberto, Diehl-Schmid, Janine, Alexopoulos, Panagiotis, Perneczky, Robert, Synofzik, Matthis, Just, Jennifer, Schöls, Ludger, Graff, Caroline, Thonberg, Håkan, Borroni, Barbara, Padovani, Alessandro, Jordanova, Albena, Sarafov, Stayko, Tournev, Ivailo, de Mendonça, Alexandre, Miltenberger-Miltenyi, Gabriel, Simões do Couto, Frederico, Ramirez, Alfredo, Jessen, Frank, Heneka, Michael T, Gómez-Tortosa, Estrella, Danek, Adrian, Cras, Patrick, Vandenberghe, Rik, De Jonghe, Peter, De Deyn, Peter P, Sleegers, Kristel, Cruts, Marc, Van Broeckhoven, Christine, Goeman, Johan, Nuytten, Dirk, Smets, Katrien, Robberecht, Wim, Damme, Philip Van, Bleecker, Jan De, Santens, Patrick, Dermaut, Bart, Versijpt, Jan, Michotte, Alex, Ivanoiu, Adrian, Deryck, Olivier, Bergmans, Bruno, Delbeck, Jean, Bruyland, Marc, Willems, Christiana, Salmon, Eric, Pastor, Pau, Ortega-Cubero, Sara, Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Hernández, Isabel, Boada, Mercè, Ruiz, Agustín, Sorbi, Sandro, Nacmias, Benedetta, Bagnoli, Silvia, Sanchez-Valle, Raquel, Llado, Albert, Santana, Isabel, Rosário Almeida, Maria, Frisoni, Giovanni B, Maetzler, Walter, Matej, Radoslav, Fraidakis, Matthew J, Kovacs, Gabor G, Fabrizi, Gian Maria, Testi, Silvia

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A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats von van der Zee, Julie, Dillen, Lubina, Van Langenhove, Tim, Engelborghs, Sebastiaan, Philtjens, Stéphanie, Vandenbulcke, Mathieu, Sleegers, Kristel, Sieben, Anne, Bäumer, Veerle, Borroni, Barbara, Padovani, Alessandro, Archetti, Silvana, Perneczky, Robert, Diehl-Schmid, Janine, de Mendonça, Alexandre, Miltenberger-Miltenyi, Gabriel, Pimentel, José, Graff, Caroline, Chiang, Huei-Hsin, Sanchez-Valle, Raquel, Llado, Albert, Gelpi, Ellen, Santiago, Beatriz, Frisoni, Giovanni, Zanetti, Orazio, Bonvicini, Cristian, vom Hagen, Jennifer Müller, Schöls, Ludger, Heneka, Michael T., Matej, Radoslav, Parobkova, Eva, Kovacs, Gabor G., Ströbel, Thomas, Sarafov, Stayko, Tournev, Ivailo, Jordanova, Albena, Danek, Adrian, Arzberger, Thomas, Testi, Silvia, Salmon, Eric, Santens, Patrick, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter Paul, Cruts, Marc, Van Broeckhoven, Christine, van der Zee, Julie, Dillen, Lubina, Van Langenhove, Tim, Philtjens, Stéphanie, Sleegers, Kristel, Corsmit, Ellen, Cruts, Marc, Van Broeckhoven, Christine, Engelborghs, Sebastiaan, De Deyn, Peter P., Cras, Patrick, Vandenbulcke, Mathieu, Borroni, Barbara, Padovani, Alessandro, Archetti, Silvana, Maetzler, Walter, Heneka, Michael T., Jessen, Frank, Kurzwelly, Delia, Sachtleben, Carmen, Miltenberger-Miltenyi, Gabriel, Pereira, Sónia, Firmo, Clara, Pimentel, José, Llado, Albert, Antonell, Anna, Gelpi, Ellen, Kinhult Ståhlbom, Anne, Thonberg, Håkan, Nennesmo, Inger, Börjesson-Hanson, Anne, Bagnoli, Silvia, Sorbi, Sandro, Santiago, Beatriz, Helena Ribeiro, Maria, Garret, Carolina, Pires, Paula, Frisoni, Giovanni, Zanetti, Orazio, Bonvicini, Cristian, Sarafov, Stayko, Tournev, Ivailo, Jordanova, Albena, Ströbel, Thomas, Mairer, Wolfgang, Matej, Radoslav, Parobkova, Eva, Danel, Adrian, Arzberger, Thomas, Maria Fabrizi, Gian, Testi, Silvia, Ferrari, Sergio, Cavallaro, Tiziana, Salmon, Eric

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Distinct Clinical Characteristics of C9orf72 Expansion Carriers Compared With GRN, MAPT, and Nonmutation Carriers in a Flanders-Belgian FTLD Cohort von Van Langenhove, Tim, van der Zee, Julie, Gijselinck, Ilse, Engelborghs, Sebastiaan, Vandenberghe, Rik, Vandenbulcke, Mathieu, De Bleecker, Jan, Sieben, Anne, Versijpt, Jan, Ivanoiu, Adrian, Deryck, Olivier, Willems, Christiana, Dillen, Lubina, Philtjens, Stéphanie, Maes, Githa, Bäumer, Veerle, Van Den Broeck, Marleen, Mattheijssens, Maria, Peeters, Karin, Martin, Jean-Jacques, Michotte, Alex, Santens, Patrick, De Jonghe, Peter, Cras, Patrick, De Deyn, Peter P, Cruts, Marc, Van Broeckhoven, Christine

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Clinical Evidence for Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion (S21.006) von Van Mossevelde, Sara, Van Der Zee, Julie, Gijselinck, Ilse, Sleegers, Kristel, Van Langenhove, Tim, Sieben, Anne, De Bleecker, Jan, Ivanoiu, Adrian, Deryck, Olivier, Santens, Patrick, Baumer, Veerle, Van Den Broeck, Marleen, Mattheijssens, Maria, Peeters, Karin, De Jonghe, Peter, De Deyn, Peter, Cras, Patrick, Vandenberghe, Rik, Martin, Jean-Jacques, Cruts, Marc, Engelborghs, Sebastiaan, 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, Stephanie, Heeman, Bavo, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu, De Baets, Greet, Baumer, 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, De Bleecker, Jan, Santens, Patrick, Dermaut, Bart, BELNEU consortium, the

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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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C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment von Cacace, Rita, Van Cauwenberghe, Caroline, Bettens, Karolien, Gijselinck, Ilse, van der Zee, Julie, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu, Van Dongen, Jasper, Bäumer, Veerle, Dillen, Lubina, Mattheijssens, Maria, Peeters, Karin, Cruts, Marc, Vandenberghe, Rik, De Deyn, Peter P., Van Broeckhoven, Christine, 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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TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis von van der Zee, Julie, Gijselinck, Ilse, Van Mossevelde, Sara, Perrone, Federica, Dillen, Lubina, Heeman, Bavo, Bäumer, Veerle, Engelborghs, Sebastiaan, De Bleecker, Jan, Baets, Jonathan, Gelpi, Ellen, Rojas-García, Ricardo, Clarimón, Jordi, Lleó, Alberto, Diehl-Schmid, Janine, Alexopoulos, Panagiotis, Perneczky, Robert, Synofzik, Matthis, Just, Jennifer, Schöls, Ludger, Graff, Caroline, Thonberg, Håkan, Borroni, Barbara, Padovani, Alessandro, Jordanova, Albena, Sarafov, Stayko, Tournev, Ivailo, de Mendonça, Alexandre, Miltenberger-Miltényi, Gabriel, Simões do Couto, Frederico, Ramirez, Alfredo, Jessen, Frank, Heneka, Michael T, Gómez-Tortosa, Estrella, Danek, Adrian, Cras, Patrick, Vandenberghe, Rik, De Jonghe, Peter, De Deyn, Peter P, Sleegers, Kristel, Cruts, Marc, Van Broeckhoven, Christine, Belgian Neurology Consortium, the, Santens, Patrick, Dermaut, Bart

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TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis von van der Zee, Julie, Gijselinck, Ilse, Van Mossevelde, Sara, Perrone, Federica, Dillen, Lubina, Heeman, Bavo, Bäumer, Veerle, Engelborghs, Sebastiaan, de Bleecker, Jan, Baets, Jonathan, Gelpi, Ellen, Rojas-García, Ricardo, Clarimón, Jordi, Lleó, Alberto, Diehl-Schmid, Janine, Alexopoulos, Panagiotis, Perneczky, Robert, Synofzik, Matthis, Just, Jennifer, Schöls, Ludger, Graff, Caroline, Thonberg, Håkan, Borroni, Barbara, Padovani, Alessandro, Jordanova, Albena, Sarafov, Stayko, Tournev, Ivailo, de Mendonça, Alexandre, Miltenberger-Miltényi, Gabriel, Simões do Couto, Frederico, Ramirez, Alfredo, Jessen, Frank, Heneka, Michael T, Gómez-Tortosa, Estrella, Danek, Adrian, Cras, Patrick, Vandenberghe, Rik, De Jonghe, Peter, De Deyn, Peter P, Sleegers, Kristel, Cruts, Marc, Van Broeckhoven, Christine, Goeman, Johan, Nuytten, Dirk, Smets, Katrien, Robberecht, Wim, Van Damme, Philip, Bleecker, Jan De, Santens, Patrick, Dermaut, Bart, Versijpt, Jan, Michotte, Alex, Ivanoiu, Adrian, Deryck, Olivier, Bergmans, Bruno, Delbeck, Jean, Bruyland, Marc, Willems, Christiana, Salmon, Eric, Pastor, Pau, Ortega-Cubero, Sara, Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Hernández, Isabel, Boada, Mercè, Ruiz, Agustín, Sorbi, Sandro, Nacmias, Benedetta, Bagnoli, Silvia, Sanchez-Valle, Raquel, Llado, Albert, Santana, Isabel, Rosário Almeida, Maria, Frisoni, Giovanni B, Maetzler, Walter, Matej, Radoslav, Fraidakis, Matthew J, Kovacs, Gabor G, Fabrizi, Gian Maria, Testi, Silvia

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C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment von Cacace, Rita, Van Cauwenberghe, Caroline, Bettens, Karolien, Gijselinck, Ilse, van der Zee, Julie, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu, Van Dongen, Jasper, Bäumer, Veerle, Dillen, Lubina, Mattheijssens, Maria, Peeters, Karin, Cruts, Marc, Vandenberghe, Rik, De Deyn, Peter P, Van Broeckhoven, Christine, Sleegers, Kristel

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C9orf72 G4 C2 repeat expansions in Alzheimer's disease and mild cognitive impairment von Cacace, Rita, Van Cauwenberghe, Caroline, Bettens, Karolien, Gijselinck, Ilse, van der Zee, Julie, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu, Van Dongen, Jasper, Bäumer, Veerle, Dillen, Lubina, Mattheijssens, Maria, Peeters, Karin, Cruts, Marc, Vandenberghe, Rik, De Deyn, Peter P, Van Broeckhoven, Christine, Sleegers, Kristel

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Distinct Clinical Characteristics of C9orf72 Expansion Carriers Compared With GRN, MAPT, and Nonmutation Carriers in a Flanders-Belgian FTLD Cohort von Van Langenhove, Tim, van der Zee, Julie, Gijselinck, Ilse, Engelborghs, Sebastiaan, Vandenberghe, Rik, Vandenbulcke, Mathieu, de Bleecker, Jan, Sieben, Anne, Versijpt, Jan, Ivanoiu, Adrian, Deryck, Olivier, Willems, Christiana, Dillen, Lubina, Philtjens, Stéphanie, Maes, Githa, Bäumer, Veerle, Van Den Broeck, Marleen, Mattheijssens, Maria, Peeters, Karin, Martin, Jean-Jacques, Michotte, Alex, Santens, Patrick, De Jonghe, Peter, Cras, Patrick, De Deyn, Peter P, Cruts, Marc, Van Broeckhoven, Christine

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Genomic characterization of the C9orf72 promoter repeat in FTLD and ALS patients von Gijselinck, Ilse, Van Langenhove, Tim, van der Zee, Julie, Philtjens, Stéphanie, Engelborghs, Sebastiaan, De Jonghe, Peter, Vandenberghe, Rik, Santens, Patrick, De Bleecker, Jan, Bäumer, Veerle, Maes, Githa, Dillen, Lubina, Cras, Patrick, Robberecht, Wim, De Deyn, Peter, Van Broeckhoven, Christine, Cruts, Marc

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A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identifi cat... von Gijselinck, Ilse, Van Langenhove, Tim, van der Zee, Julie, Sleegers, Kristel, Philtjens, Stéphanie, Kleinberger, Gernot, Janssens, Jonathan, Bettens, Karolien, Van Cauwenberghe, Caroline, Pereson, Sandra, Engelborghs, Sebastiaan, Sieben, Anne, De Jonghe, Peter, Vandenberghe, Rik, Santens, Patrick, De Bleecker, Jan, Maes, Githa, Bäumer, Veerle, Dillen, Lubina, Joris, Geert, Cuijt, Ivy, Corsmit, Ellen, Elinck, Ellen, Van Dongen, Jasper, Vermeulen, Steven, Van den Broeck, Marleen, Vaerenberg, Carolien, Mattheijssens, Maria, Peeters, Karin, Robberecht, Wim, Cras, Patrick, Martin, Jean-Jacques, De Deyn, Peter P, Cruts, Marc, Van Broeckhoven, Christine

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A Pan‐ E uropean Study of the C9orf72 Repeat Associated with FTLD : Geographic Prevalence, Genomic Instability, and Intermediate Repeats von van der Zee, Julie, Gijselinck, Ilse, Dillen, Lubina, Van Langenhove, Tim, Theuns, Jessie, Engelborghs, Sebastiaan, Philtjens, Stéphanie, Vandenbulcke, Mathieu, Sleegers, Kristel, Sieben, Anne, Bäumer, Veerle, Maes, Githa, Corsmit, Ellen, Borroni, Barbara, Padovani, Alessandro, Archetti, Silvana, Perneczky, Robert, Diehl‐Schmid, Janine, de Mendonça, Alexandre, Miltenberger‐Miltenyi, Gabriel, Pereira, Sónia, Pimentel, José, Nacmias, Benedetta, Bagnoli, Silvia, Sorbi, Sandro, Graff, Caroline, Chiang, Huei‐Hsin, Westerlund, Marie, Sanchez‐Valle, Raquel, Llado, Albert, Gelpi, Ellen, Santana, Isabel, Almeida, Maria Rosário, Santiago, Beatriz, Frisoni, Giovanni, Zanetti, Orazio, Bonvicini, Cristian, Synofzik, Matthis, Maetzler, Walter, vom Hagen, Jennifer Müller, Schöls, Ludger, Heneka, Michael T., Jessen, Frank, Matej, Radoslav, Parobkova, Eva, Kovacs, Gabor G., Ströbel, Thomas, Sarafov, Stayko, Tournev, Ivailo, Jordanova, Albena, Danek, Adrian, Arzberger, Thomas, Fabrizi, Gian Maria, Testi, Silvia, Salmon, Eric, Santens, Patrick, Martin, Jean‐Jacques, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter Paul, Cruts, Marc, Van Broeckhoven, Christine, van der Zee, Julie, Gijselinck, Ilse, Dillen, Lubina, Van Langenhove, Tim, Theuns, Jessie, Philtjens, Stéphanie, Sleegers, Kristel, Bäumer, Veerle, Maes, Githa, Corsmit, Ellen, Cruts, Marc, Van Broeckhoven, Christine, Engelborghs, Sebastiaan, De Deyn, Peter P., Cras, Patrick, Vandenbulcke, Mathieu, Borroni, Barbara, Padovani, Alessandro, Archetti, Silvana, Perneczky, Robert, Diehl‐Schmid, Janine, Synofzik, Matthis, Maetzler, Walter, Müller vom Hagen, Jennifer, Schöls, Ludger, Heneka, Michael T., Jessen, Frank, Ramirez, Alfredo, Kurzwelly, Delia, Sachtleben, Carmen, Mairer, Wolfgang, de Mendonça, Alexandre, Miltenberger‐Miltenyi, Gabriel, Pereira, Sónia, Firmo, Clara, Pimentel, José, Sanchez‐Valle, Raquel, Llado, Albert

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A Pan-European study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability and Intermediate Repeats von van der Zee, Julie, Gijselinck, Ilse, Dillen, Lubina, Van Langenhove, Tim, Theuns, Jessie, Engelborghs, Sebastiaan, Philtjens, Stéphanie, Vandenbulcke, Mathieu, Sleegers, Kristel, Sieben, Anne, Bäumer, Veerle, Maes, Githa, Corsmit, Ellen, Borroni, Barbara, Padovani, Alessandro, Archetti, Silvana, Perneczky, Robert, Diehl-Schmid, Janine, de Mendonça, Alexandre, Miltenberger-Miltenyi, Gabriel, Pereira, Sónia, Pimentel, José, Nacmias, Benedetta, Bagnoli, Silvia, Sorbi, Sandro, Graff, Caroline, Chiang, Huei-Hsin, Westerlund, Marie, Sanchez-Valle, Raquel, Llado, Albert, Gelpi, Ellen, Santana, Isabel, Almeida, Maria Rosário, Santiago, Beatriz, Frisoni, Giovanni, Zanetti, Orazio, Bonvicini, Cristian, Synofzik, Matthis, Maetzler, Walter, Vom Hagen, Jennifer Müller, Schöls, Ludger, Heneka, Michael T, Jessen, Frank, Matej, Radoslav, Parobkova, Eva, Kovacs, Gabor G, Ströbel, Thomas, Sarafov, Stayko, Tournev, Ivailo, Jordanova, Albena, Danek, Adrian, Arzberger, Thomas, Fabrizi, Gian Maria, Testi, Silvia, Salmon, Eric, Santens, Patrick, Martin, Jean-Jacques, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter Paul, Cruts, Marc, Van Broeckhoven, Christine, on behalf of the European Early-Onset Dementia (EOD) Consortium

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P4‐142: Genomic characterization of the C9orf72 promoter repeat in FTLD and ALS patients von Gijselinck, Ilse, Van Langenhove, Tim, Zee, Julie, Philtjens, Stéphanie, Engelborghs, Sebastiaan, De Jonghe, Peter, Vandenberghe, Rik, Santens, Patrick, De Bleecker, Jan, Bäumer, Veerle, Maes, Githa, Dillen, Lubina, Cras, Patrick, Robberecht, Wim, De Deyn, Peter, Van Broeckhoven, Christine, Cruts, Marc

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