Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy von Ajit Bolar, Nikhita, Vanlander, Arnaud Vincent, Wilbrecht, Claudia, Van der Aa, Nathalie, Smet, Joél, De Paepe, Boel, Vandeweyer, Geert, Kooy, Frank, Eyskens, François, De Latter, Elien, Delanghe, Gwenda, Govaert, Paul, Leroy, Jules Gerard, Loeys, Bart, Lill, Roland, Van Laer, Lut, Van Coster, Rudy

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Event rate and event-related potentials in ADHD von Wiersema, Roeljan, Van Der Meere, Jaap, Roeyers, Herbert, Van, Coster, Rudy, Baeyens, Dieter

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Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorder von Coughlin, Curtis R, Scharer, Gunter H, Friederich, Marisa W, Yu, Hung-Chun, Geiger, Elizabeth A, Creadon-Swindell, Geralyn, Collins, Abigail E, Vanlander, Arnaud V, Coster, Rudy Van, Powell, Christopher A, Swanson, Michael A, Minczuk, Michal, Van Hove, Johan L K, Shaikh, Tamim H

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Reliability of near infrared spectroscopy (NIRS) for measuring forearm oxygenation during incremental handgrip exercise von Celie, Bert, Boone, Jan, Van Coster, Rudy, Bourgois, Jan

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Linezolid-Induced Inhibition of Mitochondrial Protein Synthesis von De Vriese, An S., Van Coster, Rudy, Smet, Joél, Seneca, Sara, Lovering, Andrew, Van Haute, Lindsey L., Vanopdenbosch, Ludo J., Martin, Jean-Jacques, Ceuterick-de Groote, Chantal, Vandecasteele, Stefaan, Boelaert, Johan R.

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Characteristics, Early Development and Outcome of Parent-Reported Regression in Autism Spectrum Disorder von Boterberg, Sofie, Van Coster, Rudy, Roeyers, Herbert

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Urine lactate concentration as a non-invasive screener for metabolic abnormalities: Findings in children with autism spectrum disorder and regression von Boterberg, Sofie, Vantroys, Elise, De Paepe, Boel, Van Coster, Rudy, Roeyers, Herbert

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Expanding the Spectrum of MERS Type 2 Lesions, a Particular Form of Encephalitis von Notebaert, Anneleen, MD, Willems, Jef, MD, Coucke, Line, MSc, Van Coster, Rudy, PhD, Verhelst, Helene, MD

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Urine lactate concentration as a non-invasive screener for metabolic abnormalities: Findings in children with autism spectrum disorder and regression von Sofie Boterberg, Elise Vantroys, Boel De Paepe, Rudy Van Coster, Herbert Roeyers

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Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients von Irobi, Joy, Holmgren, Anne, Winter, Vicky De, Asselbergh, Bob, Gettemans, Jan, Adriaensen, Dirk, Groote, Chantal Ceuterick-de, Coster, Rudy Van, Jonghe, Peter De, Timmerman, Vincent

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Phenotypic spectrum of the RBM10‐mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features von Kumps, Candy, D'haenens, Erika, Vergult, Sarah, Leus, Jasmine, Coster, Rudy, Jansen, Anna, Devriendt, Koen, Oostra, Anna, Vanakker, Olivier M.

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RFC1 repeat expansions: A recurrent cause of sensory and autonomic neuropathy with cough and ataxia von Beijer, Danique, Dohrn, Maike F., Winter, Jonathan, Fazal, Sarah, Cortese, Andrea, Stojkovic, Tanya, Fernández‐Eulate, Gorka, Remiche, Gauthier, Gentile, Mattia, Coster, Rudy, Dufke, Claudia, Synofzik, Matthis, Jonghe, Peter, Züchner, Stephan, Baets, Jonathan

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A De Novo Mutation in the β-Tubulin Gene TUBB4A Results in the Leukoencephalopathy Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum von Simons, Cas, Wolf, Nicole I., McNeil, Nathan, Caldovic, Ljubica, Devaney, Joseph M., Takanohashi, Asako, Crawford, Joanna, Ru, Kelin, Grimmond, Sean M., Miller, David, Tonduti, Davide, Schmidt, Johanna L., Chudnow, Robert S., van Coster, Rudy, Lagae, Lieven, Kisler, Jill, Sperner, Jürgen, van der Knaap, Marjo S., Schiffmann, Raphael, Taft, Ryan J., Vanderver, Adeline

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The long non-coding RNA SAMMSON is essential for uveal melanoma cell survival von Dewaele, Shanna, Delhaye, Louis, De Paepe, Boel, de Bony, Eric James, De Wilde, Jilke, Vanderheyden, Katrien, Anckaert, Jasper, Yigit, Nurten, Nuytens, Justine, Vanden Eynde, Eveline, Smet, Joél, Verschoore, Maxime, Nemati, Fariba, Decaudin, Didier, Rodrigues, Manuel, Zhao, Peihua, Jochemsen, Aart, Leucci, Eleonora, Vandesompele, Jo, Van Dorpe, Jo, Marine, Jean-Christophe, Van Coster, Rudy, Eyckerman, Sven, Mestdagh, Pieter

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A Critical Assessment of the Therapeutic Potential of Resveratrol Supplements for Treating Mitochondrial Disorders von De Paepe, Boel, Van Coster, Rudy

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Possible Pathogenic Mechanism of Propofol Infusion Syndrome Involves Coenzyme Q von Vanlander, Arnaud Vincent, Okun, Juergen Guenther, de Jaeger, Annick, Smet, Joél, De Latter, Elien, De Paepe, Boel, Dacremont, Georges, Wuyts, Birgitte, Vanheel, Bert, De Paepe, Peter, Jorens, Philippe Germaine, Van Regenmortel, Niels, Van Coster, Rudy

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Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function von Morais, Vanessa A., Verstreken, Patrik, Roethig, Anne, Smet, Joél, Snellinx, An, Vanbrabant, Mieke, Haddad, Dominik, Frezza, Christian, Mandemakers, Wim, Vogt‐Weisenhorn, Daniela, Van Coster, Rudy, Wurst, Wolfgang, Scorrano, Luca, De Strooper, Bart

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Diagnostic utility of small fiber analysis in skin biopsies from children with chronic pain von Görlach, Jonas, Amsel, Daniel, Kölbel, Heike, Grzybowsky, Michelle, Rutsch, Frank, Schlierbach, Hannah, Vanlander, Arnaud, Pogatzki‐Zahn, Esther, Habig, Kathrin, Garkisch, Stefanie, Müller, Verena, Fritz, Thorsten, Ziegler, Andreas, Hahn, Andreas, Krämer, Heidrun H., Van Coster, Rudy, Schänzer, Anne

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Steroids in intractable childhood epilepsy: Clinical experience and review of the literature von Verhelst, Helene, Boon, Paul, Buyse, Gunnar, Ceulemans, Berten, D’Hooghe, Marc, Meirleir, Linda De, Hasaerts, Danièle, Jansen, An, Lagae, Lieven, Meurs, Alfred, Coster, Rudy Van, Vonck, Kristl

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High-resolution breakpoint junction mapping of proximally extended D4Z4 deletions in FSHD1 reveals evidence for a founder effect von Lemmers, Richard J L F, van der Vliet, Patrick J, Granado, David San Leon, van der Stoep, Nienke, Buermans, Henk, van Schendel, Robin, Schimmel, Joost, de Visser, Marianne, van Coster, Rudy, Jeanpierre, Marc, Laforet, Pascal, Upadhyaya, Meena, van Engelen, Baziel, Sacconi, Sabrina, Tawil, Rabi, Voermans, Nicol C, Rogers, Mark, van der Maarel, Silvère M

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