Self-healing soft pneumatic robots
Terryn, Seppe, Brancart, Joost, Lefeber, Dirk, Van Assche, Guy, Vanderborght, Bram
Published in Science robotics (16.08.2017)
Published in Science robotics (16.08.2017)
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Congenital disorders of glycosylation (CDG): Quo vadis?
Péanne, Romain, de Lonlay, Pascale, Foulquier, François, Kornak, Uwe, Lefeber, Dirk J., Morava, Eva, Pérez, Belén, Seta, Nathalie, Thiel, Christian, Van Schaftingen, Emile, Matthijs, Gert, Jaeken, Jaak
Published in European journal of medical genetics (01.11.2018)
Published in European journal of medical genetics (01.11.2018)
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Journal Article
Clinical glycomics for the diagnosis of congenital disorders of glycosylation
Abu Bakar, Nurulamin, Lefeber, Dirk J., van Scherpenzeel, Monique
Published in Journal of inherited metabolic disease (01.05.2018)
Published in Journal of inherited metabolic disease (01.05.2018)
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A Review of Gait Phase Detection Algorithms for Lower Limb Prostheses
Vu, Huong Thi Thu, Dong, Dianbiao, Cao, Hoang-Long, Verstraten, Tom, Lefeber, Dirk, Vanderborght, Bram, Geeroms, Joost
Published in Sensors (Basel, Switzerland) (17.07.2020)
Published in Sensors (Basel, Switzerland) (17.07.2020)
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Readily Accessible Bicyclononynes for Bioorthogonal Labeling and Three-Dimensional Imaging of Living Cells
Dommerholt, Jan, Schmidt, Samuel, Temming, Rinske, Hendriks, Linda J.A, Rutjes, Floris P.J.T, van Hest, Jan C.M, Lefeber, Dirk J, Friedl, Peter, van Delft, Floris L
Published in Angewandte Chemie (International ed.) (03.12.2010)
Published in Angewandte Chemie (International ed.) (03.12.2010)
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Clinical Utility Gene Card for: PGM3 defective congenital disorder of glycosylation
Jaeken, Jaak, Lefeber, Dirk J, Matthijs, Gert
Published in European journal of human genetics : EJHG (01.11.2019)
Published in European journal of human genetics : EJHG (01.11.2019)
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SRD5A3 defective congenital disorder of glycosylation: clinical utility gene card
Jaeken, Jaak, Lefeber, Dirk J, Matthijs, Gert
Published in European journal of human genetics : EJHG (01.09.2020)
Published in European journal of human genetics : EJHG (01.09.2020)
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Omics Biomarkers in Ophthalmology
Lauwen, Susette, de Jong, Eiko K, Lefeber, Dirk J, den Hollander, Al
Published in Investigative ophthalmology & visual science (01.05.2017)
Published in Investigative ophthalmology & visual science (01.05.2017)
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Clinical diagnostics and therapy monitoring in the congenital disorders of glycosylation
Van Scherpenzeel, Monique, Willems, Esther, Lefeber, Dirk J.
Published in Glycoconjugate journal (01.06.2016)
Published in Glycoconjugate journal (01.06.2016)
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Deciphering the Glycosylome of Dystroglycanopathies Using Haploid Screens for Lassa Virus Entry
Jae, Lucas T., Raaben, Matthijs, Riemersma, Moniek, van Beusekom, Ellen, Blomen, Vincent A., Velds, Arno, Kerkhoven, Ron. M., Carette, Jan E., Topaloglu, Haluk, Meinecke, Peter, Wessels, Marja W., Lefeber, Dirk J., Whelan, Sean P., van Bokhoven, Hans, Brummelkamp, Thijn R.
Published in Science (American Association for the Advancement of Science) (26.04.2013)
Published in Science (American Association for the Advancement of Science) (26.04.2013)
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Variable Stiffness Actuators: Review on Design and Components
Wolf, Sebastian, Grioli, Giorgio, Eiberger, Oliver, Friedl, Werner, Grebenstein, Markus, Hoppner, Hannes, Burdet, Etienne, Caldwell, Darwin G., Carloni, Raffaella, Catalano, Manuel G., Lefeber, Dirk, Stramigioli, Stefano, Tsagarakis, Nikos, Van Damme, Michael, Van Ham, Ronald, Vanderborght, Bram, Visser, Ludo C., Bicchi, Antonio, Albu-Schaffer, Alin
Published in IEEE/ASME transactions on mechatronics (01.10.2016)
Published in IEEE/ASME transactions on mechatronics (01.10.2016)
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Desialylation of platelets induced by Von Willebrand Factor is a novel mechanism of platelet clearance in dengue
Riswari, Silvita Fitri, Tunjungputri, Rahajeng N, Kullaya, Vesla, Garishah, Fadel M, Utari, Gloria S R, Farhanah, Nur, Overheul, Gijs J, Alisjahbana, Bachti, Gasem, M Hussein, Urbanus, Rolf T, de Groot, Philip G, Lefeber, Dirk J, van Rij, Ronald P, van der Ven, Andre, de Mast, Quirijn
Published in PLoS pathogens (01.03.2019)
Published in PLoS pathogens (01.03.2019)
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Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation
Lefeber, Dirk J, de Brouwer, Arjan P M, Morava, Eva, Riemersma, Moniek, Schuurs-Hoeijmakers, Janneke H M, Absmanner, Birgit, Verrijp, Kiek, van den Akker, Willem M R, Huijben, Karin, Steenbergen, Gerry, van Reeuwijk, Jeroen, Jozwiak, Adam, Zucker, Nili, Lorber, Avraham, Lammens, Martin, Knopf, Carlos, van Bokhoven, Hans, Grünewald, Stephanie, Lehle, Ludwig, Kapusta, Livia, Mandel, Hanna, Wevers, Ron A
Published in PLoS genetics (01.12.2011)
Published in PLoS genetics (01.12.2011)
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A Multiplex Assay for the Diagnosis of Mucopolysaccharidoses and Mucolipidoses
Langereis, Eveline J, Wagemans, Tom, Kulik, Wim, Lefeber, Dirk J, van Lenthe, Henk, Oussoren, Esmee, van der Ploeg, Ans T, Ruijter, George J, Wevers, Ron A, Wijburg, Frits A, van Vlies, Naomi
Published in PloS one (25.09.2015)
Published in PloS one (25.09.2015)
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Journal Article
High-resolution mass spectrometry glycoprofiling of intact transferrin for diagnosis and subtype identification in the congenital disorders of glycosylation
van Scherpenzeel, Monique, Steenbergen, Gerry, Morava, Eva, Wevers, Ron A, Lefeber, Dirk J
Published in Translational research : the journal of laboratory and clinical medicine (01.12.2015)
Published in Translational research : the journal of laboratory and clinical medicine (01.12.2015)
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