Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis von Nosková, Lenka, Stránecký, Viktor, Hartmannová, Hana, Přistoupilová, Anna, Barešová, Veronika, Ivánek, Robert, Hůlková, Helena, Jahnová, Helena, van der Zee, Julie, Staropoli, John F., Sims, Katherine B., Tyynelä, Jaana, Van Broeckhoven, Christine, Nijssen, Peter C.G., Mole, Sara E., Elleder, Milan, Kmoch, Stanislav

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Stress granule mediated protein aggregation and underlying gene defects in the FTD-ALS spectrum von Baradaran-Heravi, Yalda, Van Broeckhoven, Christine, van der Zee, Julie

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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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The molecular basis of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum von van Langenhove, Tim, van der Zee, Julie, van Broeckhoven, Christine

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Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis von Götzl, Julia K., Mori, Kohji, Damme, Markus, Fellerer, Katrin, Tahirovic, Sabina, Kleinberger, Gernot, Janssens, Jonathan, van der Zee, Julie, Lang, Christina M., Kremmer, Elisabeth, Martin, Jean-Jacques, Engelborghs, Sebastiaan, Kretzschmar, Hans A., Arzberger, Thomas, Van Broeckhoven, Christine, Haass, Christian, Capell, Anja

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Emerging genetic complexity and rare genetic variants in neurodegenerative brain diseases von Perrone, Federica, Cacace, Rita, van der Zee, Julie, Van Broeckhoven, Christine

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Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowth von Schmid, Bettina, Hruscha, Alexander, Hogl, Sebastian, Banzhaf-Strathmann, Julia, Strecker, Katrin, van der Zee, Julie, Teucke, Mathias, Eimer, Stefan, Hegermann, Jan, Kittelmann, Maike, Kremmer, Elisabeth, Cruts, Marc, Solchenberger, Barbara, Hasenkamp, Laura, van Bebber, Frauke, Van Broeckhoven, Christine, Edbauer, Dieter, Lichtenthaler, Stefan F., Haass, Christian

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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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A novel CHCHD10 mutation implicates a Mia40‐dependent mitochondrial import deficit in ALS von Lehmer, Carina, Schludi, Martin H, Ransom, Linnea, Greiling, Johanna, Junghänel, Michaela, Exner, Nicole, Riemenschneider, Henrick, van der Zee, Julie, Van Broeckhoven, Christine, Weydt, Patrick, Heneka, Michael T, Edbauer, Dieter

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Serum biomarker for progranulin-associated frontotemporal lobar degeneration von Sleegers, Kristel, Brouwers, Nathalie, Van Damme, Philip, Engelborghs, Sebastiaan, Gijselinck, Ilse, van der Zee, Julie, Peeters, Karin, Mattheijssens, Maria, Cruts, Marc, Vandenberghe, Rik, De Deyn, Peter P., Robberecht, Wim, Van Broeckhoven, Christine

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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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Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease von Rosas, Irene, Martínez, Carmen, Clarimón, Jordi, Lleó, Alberto, Illán-Gala, Ignacio, Dols-Icardo, Oriol, Borroni, Barbara, Almeida, Maria Rosário, van der Zee, Julie, Van Broeckhoven, Christine, Bruni, Amalia C., Anfossi, Maria, Bernardi, Livia, Maletta, Raffaele, Serpente, María, Galimberti, Daniela, Scarpini, Elio, Rossi, Giacomina, Caroppo, Paola, Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Nacmias, Benedetta, Sorbi, Sandro, Piaceri, Irene, Bagnoli, Silvia, Antonell, Anna, Sánchez-Valle, Raquel, De la Casa-Fages, Beatriz, Grandas, Francisco, Diez-Fairen, Mónica, Pastor, Pau, Ferrari, Raffaele, Álvarez, Victoria, Menéndez-González, Manuel

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Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis von van der Zee, Julie, Dillen, Lubina, Baradaran-Heravi, Yalda, Gossye, Helena, Koçoğlu, Cemile, Cuyt, Ivy, Dermaut, Bart, Sieben, Anne, Baets, Jonathan, De Jonghe, Peter, Vandenberghe, Rik, De Deyn, Peter, Cras, Patrick, Engelborghs, Sebastiaan, Van Broeckhoven, Christine

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Investigating the Endo-Lysosomal System in Major Neurocognitive Disorders Due to Alzheimer's Disease, Frontotemporal Lobar Degeneration and Lewy Body Disease: Evidence for SORL1 as... von Benussi, Luisa, Longobardi, Antonio, Kocoglu, Cemile, Carrara, Matteo, Bellini, Sonia, Ferrari, Clarissa, Nicsanu, Roland, Saraceno, Claudia, Bonvicini, Cristian, Fostinelli, Silvia, Zanardini, Roberta, Catania, Marcella, Moisse, Matthieu, Van Damme, Philip, Di Fede, Giuseppe, Binetti, Giuliano, Van Broeckhoven, Christine, van der Zee, Julie, Ghidoni, Roberta

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Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study von Le Ber, Isabelle, Camuzat, Agnès, Hannequin, Didier, Pasquier, Florence, Guedj, Eric, Rovelet-Lecrux, Anne, Hahn-Barma, Valérie, van der Zee, Julie, Clot, Fabienne, Bakchine, Serge, Puel, Michèle, Ghanim, Mustapha, Lacomblez, Lucette, Mikol, Jacqueline, Deramecourt, Vincent, Lejeune, Pascal, de la Sayette, Vincent, Belliard, Serge, Vercelletto, Martine, Meyrignac, Christian, Van Broeckhoven, Christine, Lambert, Jean-Charles, Verpillat, Patrice, Campion, Dominique, Habert, Marie-Odile, Dubois, Bruno, Brice, Alexis

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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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FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration von Urwin, Hazel, Josephs, Keith A., Rohrer, Jonathan D., Mackenzie, Ian R., Neumann, Manuela, Authier, Astrid, Seelaar, Harro, Van Swieten, John C., Brown, Jeremy M., Johannsen, Peter, Nielsen, Jorgen E., Holm, Ida E., Dickson, Dennis W., Rademakers, Rosa, Graff-Radford, Neill R., Parisi, Joseph E., Petersen, Ronald C., Hatanpaa, Kimmo J., White III, Charles L., Weiner, Myron F., Geser, Felix, Van Deerlin, Vivianna M., Trojanowski, John Q., Miller, Bruce L., Seeley, William W., van der Zee, Julie, Kumar-Singh, Samir, Engelborghs, Sebastiaan, De Deyn, Peter P., Van Broeckhoven, Christine, Bigio, Eileen H., Deng, Han-Xiang, Halliday, Glenda M., Kril, Jillian J., Munoz, David G., Mann, David M., Pickering-Brown, Stuart M., Doodeman, Valerie, Adamson, Gary, Ghazi-Noori, Shabnam, Fisher, Elizabeth M. C., Holton, Janice L., Revesz, Tamas, Rossor, Martin N., Collinge, John, Mead, Simon, Isaacs, Adrian M.

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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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Subclinical epileptiform activity in the Alzheimer continuum: association with disease, cognition and detection method von Nous, Amber, Seynaeve, Laura, Feys, Odile, Wens, Vincent, De Tiège, Xavier, Van Mierlo, Pieter, Baroumand, Amir G, Nieboer, Koenraad, Allemeersch, Gert-Jan, Mangelschots, Shana, Michiels, Veronique, van der Zee, Julie, Van Broeckhoven, Christine, Ribbens, Annemie, Houbrechts, Ruben, De Witte, Sara, Wittens, Mandy Melissa Jane, Bjerke, Maria, Vanlersberghe, Caroline, Ceyssens, Sarah, Nagels, Guy, Smolders, Ilse, Engelborghs, Sebastiaan

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Sporadic Creutzfeldt-Jakob Disease and Other Proteinopathies in Comorbidity von Parobkova, Eva, van der Zee, Julie, Dillen, Lubina, Van Broeckhoven, Christine, Rusina, Robert, Matej, Radoslav

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