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Journal Article
Epilepsia, ISSN 0013-9580, 06/2016, Volume 57, Issue 6, pp. 994 - 1003
Journal Article
by der Zee, Julie and Gijselinck, Ilse and Mossevelde, Sara and Perrone, Federica and Dillen, Lubina and Heeman, Bavo and Bäumer, Veerle and Engelborghs, Sebastiaan and Bleecker, Jan and Baets, Jonathan and Gelpi, Ellen and Rojas‐García, Ricardo and Clarimón, Jordi and Lleó, Alberto and Diehl‐Schmid, Janine and Alexopoulos, Panagiotis and Perneczky, Robert and Synofzik, Matthis and Just, Jennifer and Schöls, Ludger and Graff, Caroline and Thonberg, Håkan and Borroni, Barbara and Padovani, Alessandro and Jordanova, Albena and Sarafov, Stayko and Tournev, Ivailo and Mendonça, Alexandre and Miltenberger‐Miltényi, Gabriel and Simões do Couto, Frederico and Ramirez, Alfredo and Jessen, Frank and Heneka, Michael T and Gómez‐Tortosa, Estrella and Danek, Adrian and Cras, Patrick and Vandenberghe, Rik and Jonghe, Peter and Deyn, Peter P and Sleegers, Kristel and Cruts, Marc and Broeckhoven, Christine and Goeman, Johan and Nuytten, Dirk and Smets, Katrien and Robberecht, Wim and Damme, Philip Van and Bleecker, Jan De and Santens, Patrick and Dermaut, Bart and Versijpt, Jan and Michotte, Alex and Ivanoiu, Adrian and Deryck, Olivier and Bergmans, Bruno and Delbeck, Jean and Bruyland, Marc and Willems, Christiana and Salmon, Eric and Pastor, Pau and Ortega‐Cubero, Sara and Benussi, Luisa and Ghidoni, Roberta and Binetti, Giuliano and Hernández, Isabel and Boada, Mercè and Ruiz, Agustín and Sorbi, Sandro and Nacmias, Benedetta and Bagnoli, Silvia and Sorbi, Sandro and Sanchez‐Valle, Raquel and Llado, Albert and Santana, Isabel and Rosário Almeida, Maria and Frisoni, Giovanni B and Maetzler, Walter and Matej, Radoslav and Fraidakis, Matthew J and Kovacs, Gabor G and Fabrizi, Gian Maria and Testi, Silvia and Belgian Neurology Consortium and European Early-Onset Dementia Cons
Human Mutation, ISSN 1059-7794, 03/2017, Volume 38, Issue 3, pp. 297 - 309
Journal Article
by van der Zee, Julie and Van Langenhove, Tim and Kovacs, Gabor G and Dillen, Lubina and Deschamps, William and Engelborghs, Sebastiaan and Matěj, Radoslav and Vandenbulcke, Mathieu and Sieben, Anne and Dermaut, Bart and Smets, Katrien and Van Damme, Philip and Merlin, Céline and Laureys, Annelies and Van Den Broeck, Marleen and Mattheijssens, Maria and Peeters, Karin and Benussi, Luisa and Binetti, Giuliano and Ghidoni, Roberta and Borroni, Barbara and Padovani, Alessandro and Archetti, Silvana and Pastor, Pau and Razquin, Cristina and Ortega-Cubero, Sara and Hernández, Isabel and Boada, Mercè and Ruiz, Agustín and de Mendonça, Alexandre and Miltenberger-Miltényi, Gabriel and do Couto, Frederico Simões and Sorbi, Sandro and Nacmias, Benedetta and Bagnoli, Silvia and Graff, Caroline and Chiang, Huei-Hsin and Thonberg, Håkan and Perneczky, Robert and Diehl-Schmid, Janine and Alexopoulos, Panagiotis and Frisoni, Giovanni B and Bonvicini, Christian and Synofzik, Matthis and Maetzler, Walter and vom Hagen, Jennifer Müller and Schöls, Ludger and Haack, Tobias B and Strom, Tim M and Prokisch, Holger and Dols-Icardo, Oriol and Clarimón, Jordi and Lleó, Alberto and Santana, Isabel and Almeida, Maria Rosário and Santiago, Beatriz and Heneka, Michael T and Jessen, Frank and Ramirez, Alfredo and Sanchez-Valle, Raquel and Llado, Albert and Gelpi, Ellen and Sarafov, Stayko and Tournev, Ivailo and Jordanova, Albena and Parobkova, Eva and Fabrizi, Gian Maria and Testi, Silvia and Salmon, Eric and Ströbel, Thomas and Santens, Patrick and Robberecht, Wim and De Jonghe, Peter and Martin, Jean-Jacques and Cras, Patrick and Vandenberghe, Rik and De Deyn, Peter Paul and Cruts, Marc and Sleegers, Kristel and Van Broeckhoven, Christine
Acta Neuropathologica, ISSN 0001-6322, 9/2014, Volume 128, Issue 3, pp. 397 - 410
Journal Article
Human Mutation, ISSN 1059-7794, 07/2006, Volume 27, Issue 7, pp. 686 - 695
The varied ways in which mutations in presenilins (PSEN1 and PSEN2) affect amyloid b precursor protein (APP) processing in causing early‐onset familial... 
Aβ1‐40 | APP | Aβ1‐42 | MALDI‐TOF MS | Alzheimer disease | PSEN2 | age‐of‐onset | PSEN1 | immunohistochemistry | ELISA | Immunohistochemistry | MALDI-TOF MS | Age-of-onset | Aβ1-40 | Aβ1-42
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 7/2005, Volume 170, Issue 1, pp. 127 - 139
Lysosomal storage is the most common cause of neurodegenerative brain disease in preadulthood. However, the underlying cellular mechanisms that lead to... 
Larvae | Endocytosis | Neurons | Drosophila | Neuroglia | Alleles | Photoreceptors | Cytoplasmic inclusions | Genetic mutation | Cells | GENE | ALZHEIMERS-DISEASE | MOUSE MODEL | NEURONS | TAU | NEURAL DEGENERATION | C-DISEASE | MUTATIONS | MELANOGASTER | CELL BIOLOGY | Drosophila melanogaster - embryology | Neuromuscular Junction - metabolism | Nerve Degeneration - physiopathology | Cell Survival - genetics | Nerve Degeneration - genetics | Male | Drosophila melanogaster - genetics | Endosomes - metabolism | Nerve Degeneration - metabolism | Larva - ultrastructure | Lysosomes - metabolism | Nervous System Malformations - metabolism | Larva - growth & development | Endosomes - ultrastructure | Nervous System Malformations - physiopathology | Glycogen Storage Disease - physiopathology | Female | Lysosomes - pathology | Endocytosis - genetics | Nervous System Malformations - genetics | Neuromuscular Junction - pathology | Disease Models, Animal | Microscopy, Electron, Transmission | Yolk Sac - ultrastructure | Larva - metabolism | tau Proteins - toxicity | Carbohydrate Metabolism | Glycogen Storage Disease - metabolism | Drosophila melanogaster - ultrastructure | Endosomes - pathology | Oogenesis - genetics | Neuromuscular Junction - ultrastructure | Protein Transport - genetics | Lysosomes - ultrastructure | Carrier Proteins - genetics | Animals | Glycogen Storage Disease - genetics | Yolk Sac - metabolism | Drosophila Proteins - genetics | Metabolism, Inborn errors of | Biological research | Lysosomes | Nervous system | Degeneration | Brain diseases | Biology, Experimental
Journal Article