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All Publications

Displaying 8 results.
    • Journal article
    Frontotemporal Lobar Degeneration Case with an N-Terminal TUBA4A Mutation Exhibits Reduced TUBA4A Levels in the Brain and TDP-43 Pathology
    Van Schoor, Evelien Vandenbulcke, Mathieu Bercier, Valérie Vandenberghe, Rik van der Zee, Julie Van Broeckhoven, Christine Otto, Markus Hanseeuw, Bernard[UCL] Van Damme, Philip Van Den Bosch, Ludo Thal, Dietmar Rudolf (2022) Biomolecules — Vol. 12, no. 3, p. 440 [1-13] (2022)
    • Journal article
    How robust is ACTIVLIM for the follow-up of activity limitations in patients with neuromuscular diseases?
    Batcho, Charles Sebiyo Van den Bergh, Peter[UCL] Van Damme, Philip Roy, Anna J Thonnard, Jean-Louis[UCL] Penta, Massimo[UCL] BNMDR Scientific Committee (2016) Neuromuscular Disorders — Vol. 26, no. 3, p. 211-220 (2016)
    • Journal article
    Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures.
    Vanherpe, Pieternel Fieuws, Steffen D'Hondt, Ann Bleyenheuft, Corinne Demaerel, Philippe De Bleecker, J Van den Bergh, Peter[UCL] Baets, Jonathan Remiche, Gauthier Verhoeven, Kristof Delstanche, Stéphanie Toussaint, Michel Buyse, Bertien Van Damme, Philip Depuydt, Christophe E Claeys, Kristl G (2020) Orphanet journal of rare diseases — Vol. 15, no.1, p. 83 [1-11] (2020)
    • Journal article
    Liquid–Liquid Phase Separation Enhances TDP-43 LCD Aggregation but Delays Seeded Aggregation
    Pakravan, Donya Michiels, Emiel Bratek-Skicki, Anna De Decker, Mathias Van Lindt, Joris Alsteens, David[UCL] Derclaye, Sylvie[UCL] Van Damme, Philip Schymkowitz, Joost Rousseau, Frederic Tompa, Peter Van Den Bosch, Ludo (2021) Biomolecules — Vol. 11, no.4, p. 548 (2021)
    • Journal article
    Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases.
    Schnitzler, Lukas J Schreckenbach, Tobias Nadaj-Pakleza, Aleksandra Stenzel, Werner Rushing, Elisabeth J Van Damme, Philip Ferbert, Andreas Petri, Susanne Hartmann, Christian Bornemann, Antje Meisel, Andreas Petersen, Jens A Tousseyn, Thomas Thal, Dietmar R Reimann, Jens De Jonghe, Peter Martin, Jean-Jacques Van den Bergh, Peter Y[UCL] Schulz, Jörg B Weis, Joachim Claeys, Kristl G (2017) Orphanet Journal of Rare Diseases — Vol. 12, no. 1, p. 86 [1-12] (2017)
    • Journal article
    NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients.
    Nguyen, Hung Phuoc Van Mossevelde, Sara Dillen, Lubina De Bleecker, Jan L Moisse, Matthieu Van Damme, Philip Van Broeckhoven, Christine van der Zee, Julie BELNEU Consortium Ivanoiu, Adrian[UCL] (2018) Neurobiology of aging — Vol. 61, p. 255.e1-255.e7 (2018)
    • Journal article
    Early stages of building a rare disease registry, methods and 2010 data from the Belgian Neuromuscular Disease Registry (BNMDR)
    Roy, Anna J Van den Bergh, Peter[UCL] Van Damme, Philip Doggen, Kris Van Casteren, Viviane BNMDR Scientific Committee (2014) Acta Neurologica Belgica — Vol. 115, no. 2, p. 97-104 (2014)
    • Journal article
    No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients.
    Baradaran-Heravi, Yalda Dillen, Lubina Nguyen, Hung Phuoc Van Mossevelde, Sara Baets, Jonathan De Jonghe, Peter Engelborghs, Sebastiaan De Deyn, Peter P Vandenbulcke, Mathieu Vandenberghe, Rik Van Damme, Philip Cras, Patrick Salmon, Eric Synofzik, Matthis Heutink, Peter Wilke, Carlo Simon-Sanchez, Javier Rojas-Garcia, Ricard Turon-Sans, Janina Lleó, Alberto Illán-Gala, Ignacio Clarimón, Jordi Borroni, Barbara Padovani, Alessandro Pastor, Pau Diez-Fairen, Monica Aguilar, Miquel Gelpi, Ellen Sanchez-Valle, Raquel Borrego-Ecija, Sergi Matej, Radoslav Parobkova, Eva Nacmias, Benedetta Sorbi, Sandro Bagnoli, Silvia de Mendonça, Alexandre Ferreira, Catarina Fraidakis, Matthew J Diehl-Schmid, Janine Alexopoulos, Panagiotis Almeida, Maria Rosário Santana, Isabel Van Broeckhoven, Christine van der Zee, Julie BELNEU Consortium EU EOD Consortium Ivanoiu, Adrian[UCL] (2018) Neurobiology of aging — Vol. 69, p. 293.e9-293.e11 (2018)