Sökresultat - van der Zee, Julie

TMEM106B a Novel Risk Factor for Frontotemporal Lobar Degeneration av van der Zee, Julie, Van Broeckhoven, Christine

Hämta fulltext Hämta fulltext Hämta fulltext

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

Hämta fulltext Hämta fulltext Hämta fulltext

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

Hämta fulltext Hämta fulltext Hämta fulltext

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

Hämta fulltext Hämta fulltext Hämta fulltext

TDP-43 as a possible biomarker for frontotemporal lobar degeneration: a systematic review of existing antibodies av Goossens, Joery, Vanmechelen, Eugeen, Trojanowski, John Q, Lee, Virginia MY, Van Broeckhoven, Christine, van der Zee, Julie, Engelborghs, Sebastiaan

Hämta fulltext Hämta fulltext Hämta fulltext

Promoter DNA methylation regulates progranulin expression and is altered in FTLD av Banzhaf-Strathmann, Julia, Claus, Rainer, Mücke, Oliver, Rentzsch, Kristin, van der Zee, Julie, Engelborghs, Sebastiaan, De Deyn, Peter P, Cruts, Marc, van Broeckhoven, Christine, Plass, Christoph, Edbauer, Dieter

Hämta fulltext Hämta fulltext Hämta fulltext

A novel CHCHD10 mutation implicates a Mia40‐dependent mitochondrial import deficit in ALS av 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

Hämta fulltext Hämta fulltext Hämta fulltext

Frontotemporal Lobar Degeneration Case with an N-Terminal TUBA4A Mutation Exhibits Reduced TUBA4A Levels in the Brain and TDP-43 Pathology av Van Schoor, Evelien, Vandenbulcke, Mathieu, Bercier, Valérie, Vandenberghe, Rik, van der Zee, Julie, Van Broeckhoven, Christine, Otto, Markus, Hanseeuw, Bernard, Van Damme, Philip, Van Den Bosch, Ludo, Thal, Dietmar Rudolf

Hämta fulltext Hämta fulltext Hämta fulltext

Amyloid-β(1–43) cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations av Perrone, Federica, Bjerke, Maria, Hens, Elisabeth, Sieben, Anne, Timmers, Maarten, De Roeck, Arne, Vandenberghe, Rik, Sleegers, Kristel, Martin, Jean-Jacques, De Deyn, Peter P., Engelborghs, Sebastiaan, van der Zee, Julie, Van Broeckhoven, Christine, Cacace, Rita

Hämta fulltext Hämta fulltext Hämta fulltext

Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration av 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

Hämta fulltext Hämta fulltext Hämta fulltext

Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD av van der Zee, Julie, Mariën, Peter, Crols, Roeland, Van Mossevelde, Sara, Dillen, Lubina, Perrone, Federica, Engelborghs, Sebastiaan, Verhoeven, Jo, D'aes, Tine, Ceuterick-De Groote, Chantal, Sieben, Anne, Versijpt, Jan, Cras, Patrick, Martin, Jean-Jacques, Van Broeckhoven, Christine

Hämta fulltext Hämta fulltext Hämta fulltext

TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort av van der Zee, Julie, Van Langenhove, Tim, Kleinberger, Gernot, Sleegers, Kristel, Engelborghs, Sebastiaan, Vandenberghe, Rik, Santens, Patrick, Van den Broeck, Marleen, Joris, Geert, Brys, Jolien, Mattheijssens, Maria, Peeters, Karin, Cras, Patrick, De Deyn, Peter P., Cruts, Marc, Van Broeckhoven, Christine

Hämta fulltext Hämta fulltext Hämta fulltext

Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations av Urwin, Hazel, Authier, Astrid, Nielsen, Jorgen E., Metcalf, Daniel, Powell, Caroline, Froud, Kristina, Malcolm, Denise S., Holm, Ida, Johannsen, Peter, Brown, Jeremy, Fisher, Elizabeth M.C., van der Zee, Julie, Bruyland, Marc, Van Broeckhoven, Christine, Collinge, John, Brandner, Sebastian, Futter, Clare, Isaacs, Adrian M.

Hämta fulltext Hämta fulltext Hämta fulltext

Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis av 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

Hämta fulltext Hämta fulltext Hämta fulltext

Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis av 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

Hämta fulltext Hämta fulltext

No added diagnostic value of non-phosphorylated tau fraction (p-tau(rel)) in CSF as a biomarker for differential dementia diagnosis av 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

Hämta fulltext Hämta fulltext Hämta fulltext

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... av 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

Hämta fulltext Hämta fulltext Hämta fulltext

Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowth av 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

Hämta fulltext Hämta fulltext Hämta fulltext

Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family av 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

Hämta fulltext Hämta fulltext Hämta fulltext

Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort av Van Mossevelde, Sara, van der Zee, Julie, Gijselinck, Ilse, Engelborghs, Sebastiaan, Sieben, Anne, Van Langenhove, Tim, De Bleecker, Jan, Baets, Jonathan, Vandenbulcke, Mathieu, Van Laere, Koen, Ceyssens, Sarah, Van den Broeck, Marleen, Peeters, Karin, Mattheijssens, Maria, Cras, Patrick, Vandenberghe, Rik, De Jonghe, Peter, Martin, Jean-Jacques, De Deyn, Peter P., Cruts, Marc, Van Broeckhoven, Christine

Hämta fulltext Hämta fulltext Hämta fulltext