Works by Coster, Rudy Van

Results: 49
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    Mutations in PEX10 are a cause of autosomal recessive ataxia.

    Published in:
    Annals of Neurology, 2010, v. 68, n. 2, p. 259, doi. 10.1002/ana.22035
    By:
    • Régal, Luc;
    • Ebberink, Merel S.;
    • Goemans, Nathalie;
    • Wanders, Ronald J. A.;
    • De Meirleir, Linda;
    • Jaeken, Jacques;
    • Schrooten, Maarten;
    • Van Coster, Rudy;
    • Waterham, Hans R.
    Publication type:
    Article
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    Event rate and event-related potentials in ADHD.

    Published in:
    Journal of Child Psychology & Psychiatry, 2006, v. 47, n. 6, p. 560, doi. 10.1111/j.1469-7610.2005.01592.x
    By:
    • Wiersema, Roeljan;
    • Van Der Meere, Jaap;
    • Roeyers, Herbert;
    • Van, Coster, Rudy;
    • Baeyens, Dieter
    Publication type:
    Article
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    High-resolution breakpoint junction mapping of proximally extended D4Z4 deletions in FSHD1 reveals evidence for a founder effect.

    Published in:
    Human Molecular Genetics, 2022, v. 31, n. 5, p. 748, doi. 10.1093/hmg/ddab250
    By:
    • Lemmers, Richard J L F;
    • Vliet, Patrick J van der;
    • Granado, David San Leon;
    • van der Stoep, Nienke;
    • Buermans, Henk;
    • Schendel, Robin van;
    • Schimmel, Joost;
    • Visser, Marianne de;
    • Coster, Rudy van;
    • Jeanpierre, Marc;
    • Laforet, Pascal;
    • Upadhyaya, Meena;
    • Engelen, Baziel van;
    • Sacconi, Sabrina;
    • Tawil, Rabi;
    • Voermans, Nicol C;
    • Rogers, Mark;
    • Maarel, Silvère M van der
    Publication type:
    Article
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    Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation.

    Published in:
    Nature Genetics, 2007, v. 39, n. 4, p. 534, doi. 10.1038/ng2013
    By:
    • Scheper, Gert C.;
    • van der Klok, Thom;
    • van Andel, Rob J.;
    • van Berkel, Carola G. M.;
    • Sissler, Marie;
    • Smet, Joél;
    • Muravina, Tatjana I.;
    • Serkov, Sergey V.;
    • Uziel, Graziella;
    • Bugiani, Marianna;
    • Schiffmann, Raphael;
    • Krägeloh-Mann, Ingeborg;
    • Smeitink, Jan A. M.;
    • Florentz, Catherine;
    • Van Coster, Rudy;
    • Pronk, Jan C.;
    • van der Knaap, Marjo S.
    Publication type:
    Article
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    Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.

    Published in:
    Nature Genetics, 1999, v. 23, n. 3, p. 333, doi. 10.1038/15513
    By:
    • Papadopoulou, Lefkothea C.;
    • Sue, Carolyn M.;
    • Davidson, Mercy M.;
    • Tanji, Kurenai;
    • Nishino, Ichizo;
    • Sadlock, James E.;
    • Krishna, Sindu;
    • Walker, Winsome;
    • Selby, Jeanette;
    • Glerum, D. Moira;
    • Coster, Rudy Van;
    • Lyon, Gilles;
    • Scalais, Emmanuel;
    • Lebel, Roger;
    • Kaplan, Paige;
    • Shanske, Sara;
    • De Vivo, Darryl C.;
    • Bonilla, Eduardo;
    • Hirano, Michio
    Publication type:
    Article
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    Adaptations to Task Constraints in Catching by Boys With DCD.

    Published in:
    Adapted Physical Activity Quarterly, 2006, v. 23, n. 1, p. 14, doi. 10.1123/apaq.23.1.14
    By:
    • Deconinck, Frederik J. A.;
    • De Clercq, Dirk;
    • Savelsbergh, Geert J. P.;
    • Van Coster, Rudy;
    • Oostra, Ann;
    • Dewitte, Griet;
    • Lenoir, Matthieu
    Publication type:
    Article
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    Linezolid-Induced Inhibition of Mitochondrial Protein Synthesis.

    Published in:
    Clinical Infectious Diseases, 2006, v. 42, n. 8, p. 1111, doi. 10.1086/501356
    By:
    • 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.
    Publication type:
    Article
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    No evidence for involvement of SDHD in neuroblastoma pathogenesis.

    Published in:
    BMC Cancer, 2004, v. 4, p. 1, doi. 10.1186/1471-2407-4-55
    By:
    • De Preter, Katleen;
    • Vandesompele, Jo;
    • Hoebeeck, Jasmien;
    • Vandenbroecke, Caroline;
    • Smet, Jöel;
    • Nuyts, Annick;
    • Laureys, Geneviève;
    • Combaret, Valérie;
    • Van Roy, Nadine;
    • Roels, Frank;
    • Van Coster, Rudy;
    • Praet, Marleen;
    • De Paepe, Anne;
    • Speleman, Frank
    Publication type:
    Article
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    POLG2 deficiency causes adult-onset syndromic sensory neuropathy, ataxia and parkinsonism.

    Published in:
    Annals of Clinical & Translational Neurology, 2017, v. 4, n. 1, p. 4, doi. 10.1002/acn3.361
    By:
    • Van Maldergem, Lionel;
    • Besse, Arnaud;
    • De Paepe, Boel;
    • Blakely, Emma L.;
    • Appadurai, Vivek;
    • Humble, Margaret M.;
    • Piard, Juliette;
    • Craig, Kate;
    • He, Langping;
    • Hella, Pierre;
    • Debray, François‐Guillaume;
    • Martin, Jean‐Jacques;
    • Gaussen, Marion;
    • Laloux, Patrice;
    • Stevanin, Giovanni;
    • Van Coster, Rudy;
    • Taylor, Robert W.;
    • Copeland, William C.;
    • Mormont, Eric;
    • Bonnen, Penelope E.
    Publication type:
    Article
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    Another Case of Word-Final Disfluencies.

    Published in:
    Folia Phoniatrica et Logopaedica, 2005, v. 57, n. 3, p. 148, doi. 10.1159/000084135
    By:
    • Van Borsel, John;
    • Geirnaert, Elke;
    • Van Coster, Rudy
    Publication type:
    Article
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    Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 13, p. 2590, doi. 10.1093/hmg/ddt107
    By:
    • 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
    Publication type:
    Article
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    Worldwide distribution and broader clinical spectrum of muscle–eye–brain disease.

    Published in:
    Human Molecular Genetics, 2003, v. 12, n. 5, p. 527, doi. 10.1093/hmg/ddg043
    By:
    • Taniguchi, Kiyomi;
    • Kobayashi, Kazuhiro;
    • Saito, Kayoko;
    • Yamanouchi, Hideo;
    • Ohnuma, Akira;
    • Hayashi, Yukiko K.;
    • Manya, Hiroshi;
    • Jin, Dong Kyu;
    • Lee, Munhyang;
    • Parano, Enrico;
    • Falsaperla, Raffaele;
    • Pavone, Piero;
    • Van Coster, Rudy;
    • Talim, Beril;
    • Steinbrecher, Alice;
    • Straub, Volker;
    • Nishino, Ichizo;
    • Topaloglu, Haluk;
    • Voit, Thomas;
    • Endo, Tamao
    Publication type:
    Article
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