THU-249 The role of the ferroptosis brake glutathione peroxidase 4 in a preclinical model of metabolic dysfunction-associated steatohepatitis von Peleman, Cédric, Veeckmans, Geraldine, Hassannia, Behrouz, Vits, Lieve, Van San, Emily, De Man, Joris, Van Eyck, Annelies, Kwanten, Wilhelmus J., Vonghia, Luisa, Driessen, Ann, De Winter, Benedicte, Van Steenkiste, Christophe, Francque, Sven, Vanden Berghe, Tom

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CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1 von Fransen, E, Lemmon, V, Van Camp, G, Vits, L, Coucke, P, Willems, P J

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Ferroptosis is a targetable detrimental factor in metabolic dysfunction-associated steatotic liver disease von Peleman, Cédric, Hellemans, Stig, Veeckmans, Geraldine, Arras, Wout, Zheng, Hao, Koeken, Ine, Van San, Emily, Hassannia, Behrouz, Walravens, Magali, Kayirangwa, Edissa, Beyene, Nateneal Tamerat, Van Herck, Mikhaïl Alfons, De Vos, Winnok Harald, Pintelon, Isabel, van Nassauw, Luc, Oosterlinck, Baptiste, Smet, Annemieke, Vits, Lieve, Dirinck, Eveline, Verrijken, An, De Man, Joris, Van Eyck, Annelies, Kwanten, Wilhelmus Josephus, Vonghia, Luisa, Driessen, Ann, Augustyns, Koen, Toyokuni, Shinya, De Winter, Benedicte, Van Steenkiste, Christophe, Francque, Sven, Vanden Berghe, Tom

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Unravelling the role of iron-catalysed ferroptotic cell death in non-alcoholic steatohepatitis von Peleman, Cédric, Koeken, Ine, Veeckmans, Geraldine, Van den Branden, Astrid, Van San, Emily, Hassannia, Behrouz, Van Nassauw, Luc, Goeman, Els, Driessen, Ann, Vits, Lieve, Van Eyck, Annelies, Kwanten, Wilhelmus, Vonghia, Luisa, De Man, Joris, De Winter, Benedicte, Van Steenkiste, Christophe, Vanden Berghe, Tom, Francque, Sven

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WED-446 - Unravelling the role of iron-catalysed ferroptotic cell death in non-alcoholic steatohepatitis von Peleman, Cédric, Koeken, Ine, Veeckmans, Geraldine, Van den Branden, Astrid, Van San, Emily, Hassannia, Behrouz, Van Nassauw, Luc, Goeman, Els, Driessen, Ann, Vits, Lieve, Van Eyck, Annelies, Kwanten, Wilhelmus, Vonghia, Luisa, De Man, Joris, De Winter, Benedicte, Van Steenkiste, Christophe, Vanden Berghe, Tom, Francque, Sven

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Ferroptosis is a targetable detrimental factor in metabolic dysfunction-associated steatotic liver disease von Peleman, Cédric, Hellemans, Stig, Veeckmans, Geraldine, Arras, Wout, Zheng, Hao, Koeken, Ine, Van San, Emily, Hassannia, Behrouz, Walravens, Magali, Kayirangwa, Edissa, Beyene, Nateneal Tamerat, Van Herck, Mikhaïl Alfons, De Vos, Winnok Harald, Pintelon, Isabel, van Nassauw, Luc, Oosterlinck, Baptiste, Smet, Annemieke, Vits, Lieve, Dirinck, Eveline, Verrijken, An, De Man, Joris, Van Eyck, Annelies, Kwanten, Wilhelmus Josephus, Vonghia, Luisa, Driessen, Ann, Augustyns, Koen, Toyokuni, Shinya, De Winter, Benedicte, Van Steenkiste, Christophe, Francque, Sven, Vanden Berghe, Tom

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A locus-specific mutation database for the neural cell adhesion molecule L1CAM (Xq28) von Van Camp, Guy, Fransen, Erik, Vits, Lieve, Raes, Geert, Willems, Patrick J.

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Evidence for somatic and germline mosaicism in CRASH syndrome von Vits, Lieve, Chitayat, David, van Camp, Guy, Holden, Jeanette J.A., Fransen, Erik, Willems, Patrick J.

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Segregation of the fragile X mutation from an affected male to his normal daughter von Willems, Patrick J., Roy, Bernadette Van, De Boulle, Kristel, Vits, Lieve, Reyniers, Edwin, Beck, Olivia, Dumon, Jan E., Verkerk, Annemieke, Oostra, Ben

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L1-Associated Diseases: Clinical Geneticists Divide, Molecular Geneticists Unite von Fransen, Erik, Van Camp, Guy, Vits, Lieve, Willems, Patrick J.

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A point mutation in the FMR-1 gene associated with fragile X mental retardation von Van Roy, Bernadette, Willems, Patrick J, De Boulle, Kristel, Reyniers, Edwin, Hendrickx, Jan, Van Den Bos, Feikje, Verkerk, Annemieke J.M.H, Oostra, Ben A, Vits, Lieve, de Graaff, Esther

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Positional Cloning of a Gene Involved in Hereditary Multiple Exostoses von Wuyts, Wim, Van Hul, Wim, Wauters, Jan, Nemtsova, Marina, Reyniers, Edwin, Van Hul, Els, De Boulle, Kristel, de Vries, Bert B. A., Hendrickx, Jan, Herrygers, Ilde, Bossuyt, Paul, Balemans, Wendy, Fransen, Erik, Vits, Lieve, Coucke, Paul, Nowak, Norma J., Shows, Thomas B., Mallet, Laurence, van den Ouweland, Ans M. W., McGaughran, Julie, Halley, Dicky J. J., Willems, Patrick J.

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Genotype-phenotype correlation in L1 associated diseases von Fransen, E, Van Camp, G, D'Hooge, R, Vits, L, Willems, P J

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Gonosomal mosaicism in myotonic dystrophy patients: Involvement of mitotic events in (CTG)[sub n] repeat variation and selection against extreme expansion in sperm von Jansen, G., Coerwinkel, M., Wieringa, B., Nillesen, W., Smeets, H., Brunner, H., Wieringa, B., Willems, P., Vits, L., Hoeweler, C.

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The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm von Willems, Patrick J, Reyniers, Edwin, De Boulle, Kristel, Oostra, Ben, Verkerk, Annemieke J.M.H, Velzen, Desirée Van, Jorens, Hugo Z.J, Darby, John K, Vits, Lieve, Roy, Bernadette Van, de Graaff, Esther

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Erratum to “High incidence of the CFTR mutations 3272-26A → G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A → G, E588V, and... von Storm, Katrien, Moens, Els, Vits, Lieve, De Vlieger, Haike, Delaere, Gino, D'Hollander, Maria, Wuyts, Wim, Biervliet, Martine, Van Schil, Lutgardis, Desager, Kristine, Nöthen, Markus M

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High incidence of the CFTR mutations 3272-26A → G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A → G, E588V, and 1671insTATCA... von Storm, Katrien, Moens, Els, Vits, Lieve, De Vlieger, Haike, Delaere, Gino, D'Hollander, Maria, Wuyts, Wim, Biervliet, Martine, Van Schil, Lutgardis, Desager, Kristine, Nöthen, Markus M

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MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM von Vits, Lieve, Van Camp, Guy, Coucke, Paul, Fransen, Erik, De Boulle, Kristel, Reyniers, Edwin, Korn, Bernhard, Poustka, Annemarie, Wilson, Golder, Schrander-Stumpel, Connie, Winter, Robin M, Schwartz, Charles, Willems, Patrick J

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A New Neurological Syndrome with Mental Retardation, Choreoathetosis, and Abnormal Behavior Maps to Chromosome Xp11 von Reyniers, Edwin, Van Bogaert, Patrick, Peeters, Nils, Vits, Lieve, Pauly, Fernand, Fransen, Erik, Van Regemorter, Nicole, Kooy, R. Frank

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A duplication in the L1CAM gene associated with X-linked hydrocephalus von Darby, John, Holden, Jeanette, Willems, Patrick J, Munnich, Arnold, Camp, Guy Van, Lyonnet, Stanislas, Vits, Lieve, Coucke, Paul, Schrander-Stumpel, Connie

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