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Affichage: 5 résultats.
    • Article de périodique
    TBK1Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
    van der Zee, Julie Gijselinck, Ilse Van Mossevelde, Sara Perrone, Federica Dillen, Lubina Heeman, Bavo Bâumer, Veerle Engelborghs, Sebastiaan De Bleecker, Jan Baets, Jonathan Gelpi, Ellen Rojas-García, Ricardo Clarimón, Jordi Lleó, Alberto Diehl-Schmid, Janine Alexopoulos, Panagiotis Perneczky, Robert Synofzik, Matthis Just, Jennifer Schöls, Ludger Graff, Caroline Thonberg, Hakan Borroni, Barbara Padovani, Alessandro Jordanova, Albena Sarafov, Stayko Tournev, Ivailo de Mendonça, Alexandre Miltenberger-Miltényi, Gabriel Simões do Couto, Frederico Ramirez, Alfredo Jessen, Frank Heneka, Michael T. Gómez-Tortosa, Estrella Danek, Adrian Cras, Patrick Vandenberghe, Rik De Jonghe, Peter De Deyn, Peter P. Sleegers, Kristel Cruts, Marc Van Broeckhoven, Christine Goeman, Johan Nuytten, Dirk Smets, Katrien Robberecht, Wim Damme, Philip Van Bleecker, Jan De Santens, Patrick Dermaut, Bart Versijpt, Jan Michotte, Alex Ivanoiu, Adrian[UCL] Deryck, Olivier Bergmans, Bruno Delbeck, Jean Bruyland, Marc Willems, Christiana Salmon, Eric Pastor, Pau Ortega-Cubero, Sara Benussi, Luisa Ghidoni, Roberta Binetti, Giuliano Hernàndez, Isabel Boada, Mercè Ruiz, Agustín Sorbi, Sandro Nacmias, Benedetta Bagnoli, Silvia Sorbi, Sandro Sanchez-Valle, Raquel Llado, Albert Santana, Isabel Rosàrio Almeida, Maria Frisoni, Giovanni B Maetzler, Walter Matej, Radoslav Fraidakis, Matthew J. Kovacs, Gabor G. Fabrizi, Gian Maria Testi, Silvia (2017) Human Mutation — Vol. 38, no. 3, p. 297-309 (2017)
    • Article de périodique
    Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study
    Dierick, Ines Baets, Jonathan Irobi, Joy Jacobs, An De Vriendt, Els Deconinck, Tine Merlini, Luciano Van den Bergh, Peter[UCL] Rasic, Vedrana Milic Robberecht, Wim Fischer, Dirk Morales, Raul Juntas Mitrovic, Zoran Seeman, Pavel Mazanec, Radim Kochanski, Andrzej Jordanova, Albena Auer-Grumbach, Michaela Helderman-van den Enden, A. T. J. M. Wokke, John H. J. Nelis, Eva De Jonghe, Peter Timmerman, Vincent (2008) Brain : a journal of neurology — Vol. 131, no. Pt 5, p. 1217-1227 (2008)
    • Article de périodique
    Mutations in SACS cause atypical and late-onset forms of ARSACS
    Baets, J. Van den Bergh, Peter[UCL] Deconinck, T. Smets, K. Goossens, D. Dahan, Karin[UCL] Schmedding, E. Santens, P. Rasic, V. Milic Van Damme, Patricia[UCL] Robberecht, Wim[UCL] De Meirleir, L. Michielsens, B. Del-Favero, J. Jordanova, A. De Jonghe, P. (2010) Neurology — Vol. 75, no. 13, p. 1181-8 (2010)
    • Article de périodique
    MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
    Verhoeven, Kristien Claeys, Kristl G. Züchner, Stephan Schröder, J. Michael Weis, Joachim Ceuterick, Chantal Jordanova, Albena Nelis, Eva De Vriendt, Els Van Hul, Matthias Seeman, Pavel Mazanec, Radim Saifi, Gulam Mustafa Szigeti, Kinga Mancias, Pedro Butler, Ian J. Kochanski, Andrzej Ryniewicz, Barbara De Bleecker, Jan Van den Bergh, Peter[UCL] Verellen, Christine[UCL] Van Coster, Rudy Goemans, Nathalie Auer-Grumbach, Michaela Robberecht, Wim Milic Rasic, Vedrana Nevo, Yoram Tournev, Ivajlo Guergueltcheva, Velina Roelens, Filip Vieregge, Peter Vinci, Paolo Moreno, Maria Teresa Christen, H.-J. Shy, Michael E. Lupski, James R. Vance, Jeffery M. De Jonghe, Peter Timmerman, Vincent (2006) Brain : a journal of neurology — Vol. 129, no. 8, p. 2093-2102 (2006)
    • Article de périodique
    Mibefradil (Ro 40-5967) blocks multiple types of voltage-gated calcium channels in cultured rat spinal motoneurones
    Viana, F VanDenBosch, L Missiaen, L Vandenberghe, Wim Droogmans, G Nilius, Bernd[UCL] Robberecht, Wim[UCL] (1997) Cell Calcium — Vol. 22, no. 4, p. 299-311 (1997)