A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation von Tavernier, S. J., Athanasopoulos, V., Verloo, P., Behrens, G., Staal, J., Bogaert, D. J., Naesens, L., De Bruyne, M., Van Gassen, S., Parthoens, E., Ellyard, J., Cappello, J., Morris, L. X., Van Gorp, H., Van Isterdael, G., Saeys, Y., Lamkanfi, M., Schelstraete, P., Dehoorne, J., Bordon, V., Van Coster, R., Lambrecht, B. N., Menten, B., Beyaert, R., Vinuesa, C. G., Heissmeyer, V., Dullaers, M., Haerynck, F.

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Familial chylomicronemia syndrome: a novel mutation in the lipoprotein lipase gene von Van Biervliet, S, Vande Velde, S, De Bruyne, P, Callewaert, B, Verloo, P, De Bruyne, R

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Author Correction: A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation von Tavernier, S. J., Athanasopoulos, V., Verloo, P., Behrens, G., Staal, J., Bogaert, D. J., Naesens, L., De Bruyne, M., Van Gassen, S., Parthoens, E., Ellyard, J., Cappello, J., Morris, L. X., Van Gorp, H., Van Isterdael, G., Saeys, Y., Lamkanfi, M., Schelstraete, P., Dehoorne, J., Bordon, V., Van Coster, R., Lambrecht, B. N., Menten, B., Beyaert, R., Vinuesa, C. G., Heissmeyer, V., Dullaers, M., Haerynck, F.

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TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria von Jansen, A C, Oostra, A, Desprechins, B, De Vlaeminck, Y, Verhelst, H, Régal, L, Verloo, P, Bockaert, N, Keymolen, K, Seneca, S, De Meirleir, L, Lissens, W

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PP13.9 – 2836: Variants in the NR3C2 gene as possible genetic predisposition for the development of multiple sclerosis von Verhelst, H, Mets, G, Verloo, P, D'Hooghe, M, Symons, A, Nagels, G, Menten, B, Debruyne, J, Van Coster, R, Vanakker, O

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Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes von Mefford, Heather C, Sharp, Andrew J, Baker, Carl, Itsara, Andy, Jiang, Zhaoshi, Buysse, Karen, Huang, Shuwen, Maloney, Viv K, Crolla, John A, Baralle, Diana, Collins, Amanda, Mercer, Catherine, Norga, Koen, de Ravel, Thomy, Devriendt, Koen, Bongers, Ernie M.H.F, de Leeuw, Nicole, Reardon, William, Gimelli, Giorgio, Gimelli, Stefania, Bena, Frederique, Hennekam, Raoul C, Male, Alison, Gaunt, Lorraine, Clayton-Smith, Jill, Simonic, Ingrid, Park, Soo Mi, Mehta, Sarju G, Nik-Zainal, Serena, Woods, C. Geoffrey, Firth, Helen V, Parkin, Georgina, Fichera, Marco, Reitano, Santina, Giudice, Mariangela Lo, Li, Kelly E, Casuga, Iris, Broomer, Adam, Conrad, Bernard, Schwerzmann, Markus, Räber, Lorenz, Gallati, Sabina, Striano, Pasquale, Coppola, Antonietta, Tolmie, John L, Tobias, Edward S, Lilley, Chris, Armengol, Lluis, Spysschaert, Yves, Verloo, Patrick, De Coene, Anja, Goossens, Linde, Mortier, Geert, Speleman, Frank, van Binsbergen, Ellen, Nelen, Marcel R, Hochstenbach, Ron, Poot, Martin, Gallagher, Louise, Gill, Michael, McClellan, Jon, King, Mary-Claire, Regan, Regina, Skinner, Cindy, Stevenson, Roger E, Antonarakis, Stylianos E, Chen, Caifu, Estivill, Xavier, Menten, Björn, Gribble, Susan, Schwartz, Charles E, Schwartz, Stuart, Sutcliffe, James S, Walsh, Tom, Knight, Samantha J.L, Sebat, Jonathan, Romano, Corrado, Veltman, Joris A, de Vries, Bert B.A, Vermeesch, Joris R, Barber, John C.K, Willatt, Lionel, Tassabehji, May, Eichler, Evan E

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P239 Lemierre's syndrome with bilateral occlusion of the internal carotid arteries von Verloo, P, Schelstraete, P, Verhelst, H, Van Coster, R

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P052 Hashimoto encephalopathy in Down's syndrome with dimethylargininase-1 autoantibodies von Verhelst, H, Verloo, P, De Paepe, B, Gini, B, Bonetti, B, Van Coster, R

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P303 Mechanism of lactic acidosis in patients with the propofol infusion syndrome (PRIS) von Vanlander, A, Verhelst, H, Verloo, P, de Jaeger, A, Smet, J, Van Coster, R

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P256 Anti-NMDA-receptor encephalitis in a 3 year old boy with an inherited microdeletion on chromosome 6, including the HLA cluster von Verhelst, H, Verloo, P, Dhondt, K, De Paepe, B, Menten, B, Dalmau, J, Van Coster, R

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Abdominal pain and vomiting as first sign of mitochondrial disease von VAN BIERVLIET, S, VERLOO, P, VANDE VELDE, S, VAN WINCKEL, M, SMET, J, SENECA, S, DE MEIRLEIR, L, VAN COSTER, R

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P301 Mitochondrial abnormalities in a newborn with lactic acidosis and adrenal calcifications von Van Coster, R, Smet, J, Verhelst, H, Verloo, P, Vanhaesebrouck, P, Viscomi, C, Van Den Broecke, C, De Paepe, B, De Meirleir, L, Zeviani, M, Seneca, S, Lissens, W, De Praeter, C

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P314 – 1862 Clinical and behavioral characteristics of childhood narcolepsy von Dhondt, K, Verloo, P, Verhelst, H, Van Coster, R

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Plasmodium falciparum-activated Chloride Channels Are Defective in Erythrocytes from Cystic Fibrosis Patients von Verloo, Patrick, Kocken, Clemens H.M., Van der Wel, Annemarie, Tilly, Ben C., Hogema, Boris M., Sinaasappel, Maarten, Thomas, Alan W., De Jonge, Hugo R.

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P123 – 1742 Extensive multifocal demyelinating encephalomyelitis with spectacular response to intravenous immunoglobulins von Verhelst, H, Maes, M, Meersschaut, V, Verloo, P, Van Coster, R

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Blue Native polyacrylamide gel electrophoresis: A powerful tool in diagnosis of oxidative phosphorylation defects von VAN COSTER, Rudy, SMET, Joel, VERLOO, Patrick, LEROY, Jules, GEORGE, Edith, DE MEIRLEIR, Linda, SENECA, Sara, VAN HOVE, Johan, SEBIRE, Guillaume, VERHELST, Helene, DE BLEECKER, Jan, VAN VLEM, Bruno

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P19.6 Multiple sclerosis in a 12 year old boy with an inherited microdeletion within the NR3C2 gene von Verhelst, H., Verloo, P., Menten, B., van Coster, R.

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P07.18 Cerebral Capillary Telangiectasias von Verbeek, S., Verloo, P., Verhelst, H., Achten, E., Defreyne, L., Baert, E., van Coster, R.

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1FC4.4 Neurological presentation in children with familial and acquired hemophagocytic lymphohistiocytosis von Verhelst, H., Verloo, P., Mondelaers, V., Haerynck, F., Van Coster, R., Bordon, V.

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I TUBAIA mutations: I From isolated lissencephaly to familial polymicrogyria von JANSEN, A. C, OOSTRA, A, DE MEIRLEIR, L, LISSENS, W, DESPRECHINS, B, DE VLAEMINCK, Y, VERHELST, H, REGAL, L, VERLOO, P, BOCKAERT, N, KEYMOLEN, K, SENECA, S

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