P40 – 2775: Unusual presentation in a child with a mutation in GRIN2A von Hasaerts, D, Jonckheere, A, Jansen, A, De Meirleir, L, Lederer, D

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De novo KCNQ2 mutations in patients with benign neonatal seizures von Claes, L R F, Ceulemans, B, Audenaert, D, Deprez, L, Jansen, A, Hasaerts, D, Weckx, S, Claeys, K G, Del-Favero, J, Van Broeckhoven, C, De Jonghe, P

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Prader Willi Syndrom: about 2 patients in the neonatal intensive care unit von Devogeleer, L, Rotunno, E, Van Renthergem, C, Reible, R, Vlassenrood, A, Van Herrewhege, I, Hasaerts, D, Tackoen, M

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Identification of two de novo mutations responsible for type I antithrombin deficiency von Orlando, Christelle, Lissens, Willy, Hasaerts, Daniele, Jochmans, Kristin

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A case of herpes simplex encephalitis: a diagnostic dilemma von Voets, S, Janssen, A, van Berlaer, G, Hasaerts, D, Hachimi-Idrissi, S, De Meirleir, L

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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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NMP033 Molecular analysis in congenital muscular dystrophy von De Meirleir, L, Hasaerts, D, Keymolen, K, Voets, S, De Rademaeker, M, Lissens, W, Seneca, S, Lamande, S, Quijano-Roy, S, Michotte, A

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Early onset Huntington disease: a neuronal degeneration syndrome von SENECA, Sara, FAGNART, Dominique, KEYMOLEN, Kathelijn, LISSENS, Willy, HASAERTS, Daniele, DEBULPAEP, Sara, DESPRECHINS, Brigitte, LIEBAERS, Inge, DE MEIRLEIR, Linda

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Dancing Eye Syndrome and Hyperphosphatasemia von Hasaerts, Daniele E., Gorus, Frans K., De Meirleir, Linda J.

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Phenothiazine-induced sleep apneas in normal infants von KAHN, A, HASAERTS, D, BLUM, D

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P25.6 Evaluation of follow-up of premature born children von Werckx, W., Hasaerts, D., Jansen, A., Cools, F., Eggers, N., Dereu, I., Van Den Driessche, J., De Meirleir, L.

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De novo KCNQ2 mutations in patients with benign neonatal seizures von CLAES, L. R. F, CEULEMANS, B, DE JONGHE, P, AUDENAERT, D, DEPREZ, L, JANSEN, A, HASAERTS, D, WECKX, S, CLAEYS, K. G, DEL-FAVERO, J, VAN BROECKHOVEN, C

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Early MR detection of cortical and subcortical hypoxic-ischemic encephalopathy in full-term-infants von CHRISTOPHE, C, CLERCX, A, BLUM, D, HASAERTS, D, SEGEBARTH, C, PERLMUTTER, N

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Anterior fontanelle pressure variations during sleep in healthy infants von WAYENBERG, J.-L, HASAERTS, D, FRANCO, P, VALENTE, F, MASSAAGER, N

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De novo KCNQ2 mutations in patients with benign neonatal seizures von Claes, L.R.F, Ceulemans, B, Audenaert, D, Deprez, L, Jansen, Sandra, Hasaerts, D, Weckx, Stefan, Claeys, Kristl, Del-Favero, J, Van Broeckhoven, C, De Jonghe, P

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Objets planologiques en déplacement. Vers une jurisprudence de cas ethnographiques von Houlstan-Hasaerts, Rafaella, Laki, Giulietta

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