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Affichage: 3 résultats.
    • Article de périodique
    Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy.
    Duerinckx, Sarah Désir, Julie Perazzolo, Camille Badoer, Cindy Jacquemin, Valérie Soblet, Julie Maystadt, Isabelle Tunca, Yusuf Blaumeiser, Bettina Ceulemans, Berten Courtens, Winnie Debray, François-Guillaume Destree, Anne Devriendt, Koenraad Jansen, Anna Keymolen, Kathelijn Lederer, Damien Loeys, Bart Meuwissen, Marije Moortgat, Stéphanie[UCL] Mortier, Geert Nassogne, Marie-Cécile[UCL] Sekhara, Tayeb Van Coster, Rudy Van Den Ende, Jenny Van der Aa, Nathalie Van Esch, Hilde Vanakker, Olivier Verhelst, Helene Vilain, Catheline Weckhuysen, Sarah Passemard, Sandrine Verloes, Alain Aeby, Alec Deconinck, Nicolas Van Bogaert, Patrick Pirson, Isabelle Abramowicz, Marc (2021) Molecular genetics & genomic medicine — Vol. 9, no. 9, p. e1768 [1-19] (2021)
    • Article de périodique
    Targeted Genomic Sequencing of TSC1 and TSC2 Reveals Causal Variants in Individuals for Whom Previous Genetic Testing for Tuberous Sclerosis Complex Was Normal
    West, Hannah D. Nellist, Mark Brouwer, Rutger W. W. van den Hout-van Vroonhoven, Mirjam C. G. N. de Almeida, Luiz Gustavo Dufner Hendriks, Femke Elfferich, Peter Raja, Meera Giles, Peter Alfano, Rosa M. Peron, Angela Sznajer, Yves[UCL] De Waele, Liesbeth Jansen, Anna Koopmans, Marije Kievit, Anneke Farach, Laura S. Northrup, Hope Sampson, Julian R. Thomas, Laura E. van IJcken, Wilfred F. J. Chen, Jian-Min (2023) Human Mutation — Vol. 2023, p. 4899372 [1-18] (2023)
    • Article de périodique
    First line management of prolonged convulsive seizures in children and adults: good practice points.
    De Waele, Liesbeth Boon, Paul Ceulemans, Berten Dan, Bernard Jansen, Anna Legros, Benjamin Leroy, Patricia Delmelle, Francoise Ossemann, Michel[UCL] De Raedt, Sylvie Smets, Katrien Van De Voorde, Patrick Verhelst, Helene Lagae, Lieven (2013) Acta Neurologica Belgica — Vol. 113, no.4, p. 375-380 (2013)