TMEM106B a Novel Risk Factor for Frontotemporal Lobar Degeneration

Por van der Zee, Julie, Van Broeckhoven, Christine
Publicado em 2011

The molecular basis of the frontotemporal lobar degeneration–amyotrophic lateral sclerosis spectrum

Por van Langenhove, Tim, van der Zee, Julie, van Broeckhoven, Christine
Publicado em 2012

Emerging genetic complexity and rare genetic variants in neurodegenerative brain diseases

Por Perrone, Federica, Cacace, Rita, van der Zee, Julie, Van Broeckhoven, Christine
Publicado no Genome Med (2021)

Sporadic Creutzfeldt-Jakob Disease and Other Proteinopathies in Comorbidity

Por Parobkova, Eva, van der Zee, Julie, Dillen, Lubina, Van Broeckhoven, Christine, Rusina, Robert, Matej, Radoslav
Publicado no Front Neurol (2020)

TDP-43 as a possible biomarker for frontotemporal lobar degeneration: a systematic review of existing antibodies

Por Goossens, Joery, Vanmechelen, Eugeen, Trojanowski, John Q, Lee, Virginia MY, Van Broeckhoven, Christine, van der Zee, Julie, Engelborghs, Sebastiaan
Publicado no Acta Neuropathol Commun (2015)

Promoter DNA methylation regulates progranulin expression and is altered in FTLD

Por 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
Publicado em 2013

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

Por 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
Publicado no EMBO Mol Med (2018)

Amyloid-β(1–43) cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations

Por 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
Publicado no Alzheimers Res Ther (2020)

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

Por 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
Publicado no Alzheimers Res Ther (2018)

Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD

Por 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
Publicado no Neurol Genet (2016)

TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort

Por 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
Publicado em 2011

Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations

Por 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.
Publicado em 2010

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

Por 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
Publicado em 2011

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

Por 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
Publicado em 2011

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

Por 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
Publicado no Alzheimers Res Ther (2017)

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

Por 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
Publicado em 2013

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

Por 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
Publicado no Alzheimers Res Ther (2018)

Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort

Por 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
Publicado no Neurology (2015)

Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

Por 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
Publicado no Brain (2016)

Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains

Por Janssens, Jonathan, Philtjens, Stéphanie, Kleinberger, Gernot, Van Mossevelde, Sara, van der Zee, Julie, Cacace, Rita, Engelborghs, Sebastiaan, Sieben, Anne, Banzhaf-Strathmann, Julia, Dillen, Lubina, Merlin, Céline, Cuijt, Ivy, Robberecht, Caroline, Schmid, Bettina, Santens, Patrick, Ivanoiu, Adrian, Vandenbulcke, Mathieu, Vandenberghe, Rik, Cras, Patrick, De Deyn, Peter P., Martin, Jean-Jacques, Maudsley, Stuart, Haass, Christian, Cruts, Marc, Van Broeckhoven, Christine
Publicado no Acta Neuropathol Commun (2015)