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Affichage: 11 résultats.
    • Article de périodique
    Vagus nerve stimulation for refractory epilepsy: A Belgian multicenter study
    De Herdt, Veerle Boon, Paul Ceulemans, Berten Hauman, Henri Lagae, Lieven Legros, Benjamin Sadzot, Bernard Van Bogaert, Patrick Van Rijckevorsel, Kenou[UCL] Verhelst, Helene Vonck, Kristl (2007) European Journal of Paediatric Neurology — Vol. 11, no. 5, p. 261-269 (2007)
    • Article de périodique
    Treatment and long term outcome in West syndrome: The clinical reality. A multicentre follow up study
    Lagae, Lieven[UCL] Nassogne, Marie-Cécile[UCL] Verhelst, Helene Ceulemans, Berten De Meirleir, Linda De Borchgrave, Valerie D'Hooghe, Marc Foulon, Martine Van Bogaert, Patrick (2010) Seizure - European Journal of Epilepsy — Vol. 19, no. 3, p. 159-64 (2010)
    • 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
    Genotype-phenotype correlations in patients with de novo pathogenic variants.
    Malerba, Federica Alberini, Giulio Balagura, Ganna Marchese, Francesca Amadori, Elisabetta Riva, Antonella Vari, Maria Stella Gennaro, Elena Madia, Francesca Salpietro, Vincenzo Angriman, Marco Giordano, Lucio Accorsi, Patrizia Trivisano, Marina Specchio, Nicola Russo, Angelo Gobbi, Giuseppe Raviglione, Federico Pisano, Tiziana Marini, Carla Mancardi, Maria M Nobili, Lino Freri, Elena Castellotti, Barbara Capovilla, Giuseppe Coppola, Antonietta Verrotti, Alberto Martelli, Paola Miceli, Francesco Maragliano, Luca Benfenati, Fabio Cilio, Maria-Roberta[UCL] Johannesen, Kathrine M Møller, Rikke S Ceulemans, Berten Minetti, Carlo Weckhuysen, Sarah Zara, Federico Taglialatela, Maurizio Striano, Pasquale (2020) Neurology. Genetics — Vol. 6, no.6, p. e528 [1-7] (2020)
    • Article de périodique
    Genetic spectrum of hereditary neuropathies with onset in the first year of life
    Baets, Jonathan Deconinck, Tine De Vriendt, Els Zimoń, Magdalena Yperzeele, Laetitia Van Hoorenbeeck, Kim Peeters, Kristien Spiegel, Ronen Parman, Yesim Ceulemans, Berten Van Bogaert, Patrick Pou-Serradell, Adolf Bernert, Günther Dinopoulos, Argirios Auer-Grumbach, Michaela Sallinen, Satu-Leena Fabrizi, Gian Maria Pauly, Fernand Van den Bergh, Peter[UCL] Bilir, Birdal Battaloglu, Esra Madrid, Ricardo E. Kabzińska, Dagmara Kochanski, Andrzej Topaloglu, Haluk Miller, Geoffrey Jordanova, Albena Timmerman, Vincent De Jonghe, Peter (2011) Brain : a journal of neurology — Vol. 134, no. 9, p. 2664-2676 (2011)
    • Article de périodique
    Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition.
    Palmer, Elizabeth E Pusch, Michael Picollo, Alessandra Forwood, Caitlin Nguyen, Matthew H Suckow, Vanessa Gibbons, Jessica Hoff, Alva Sigfrid, Lisa Megarbane, Andre Nizon, Mathilde Cogné, Benjamin Beneteau, Claire Alkuraya, Fowzan S Chedrawi, Aziza Hashem, Mais O Stamberger, Hannah Weckhuysen, Sarah Vanlander, Arnaud Ceulemans, Berten Rajagopalan, Sulekha Nunn, Kenneth Arpin, Stéphanie Raynaud, Martine Motter, Constance S Ward-Melver, Catherine Janssens, Katrien Meuwissen, Marije Beysen, Diane Dikow, Nicola Grimmel, Mona Haack, Tobias B Clement, Emma McTague, Amy Hunt, David Townshend, Sharron Ward, Michelle Richards, Linda J Simons, Cas Costain, Gregory Dupuis, Lucie Mendoza-Londono, Roberto Dudding-Byth, Tracy Boyle, Jackie Saunders, Carol Fleming, Emily El Chehadeh, Salima Spitz, Marie-Aude Piton, Amelie Gerard, Bénédicte Abi Warde, Marie-Thérèse Rea, Gillian McKenna, Caoimhe Douzgou, Sofia Banka, Siddharth Akman, Cigdem Bain, Jennifer M Sands, Tristan T Wilson, Golder N Silvertooth, Erin J Miller, Lauren Lederer, Damien Sachdev, Rani Macintosh, Rebecca Monestier, Olivier Karadurmus, Deniz Collins, Felicity Carter, Melissa Rohena, Luis Willemsen, Marjolein H Ockeloen, Charlotte W Pfundt, Rolph Kroft, Sanne D Field, Michael Laranjeira, Francisco E R Fortuna, Ana M Soares, Ana R Michaud, Vincent Naudion, Sophie Golla, Sailaja Weaver, David D Bird, Lynne M Friedman, Jennifer Clowes, Virginia Joss, Shelagh Pölsler, Laura Campeau, Philippe M Blazo, Maria Bijlsma, Emilia K Rosenfeld, Jill A Beetz, Christian Powis, Zöe McWalter, Kirsty Brandt, Tracy Torti, Erin Mathot, Mikaël[UCL] Mohammad, Shekeeb S Armstrong, Ruth Kalscheuer, Vera M (2023) Molecular psychiatry — Vol. 28, no. 2, p. 668-697 (2023)
    • Article de périodique
    FOXP1 -related intellectual disability syndrome: a recognisable entity
    Meerschaut, Ilse Rochefort, Daniel Revencu, Nicole[UCL] Pètre, Justine Corsello, Christina Rouleau, Guy A Hamdan, Fadi F Michaud, Jacques L Morton, Jenny Radley, Jessica Ragge, Nicola García-Miñaúr, Sixto Lapunzina, Pablo Bralo, Maria Palomares Mori, Maria Ángeles Moortgat, Stéphanie Benoit, Valérie Mary, Sandrine Bockaert, Nele Oostra, Ann Vanakker, Olivier Velinov, Milen de Ravel, Thomy JL Mekahli, Djalila Sebat, Jonathan Vaux, Keith K DiDonato, Nataliya Hanson-Kahn, Andrea K Hudgins, Louanne Dallapiccola, Bruno Novelli, Antonio Tarani, Luigi Andrieux, Joris Parker, Michael J Neas, Katherine Ceulemans, Berten Schoonjans, An-Sofie Prchalova, Darina Havlovicova, Marketa Hancarova, Miroslava Budisteanu, Magdalena Dheedene, Annelies Menten, Björn Dion, Patrick A Lederer, Damien Callewaert, Bert (2017) Journal of Medical Genetics — Vol. 54, no.9, p. 613-623 (2017)
    • Article de périodique
    Autosomal recessive primary microcephaly due to ASPM mutations: An update
    Létard, Pascaline Drunat, Séverine Vial, Yoann Duerinckx, Sarah Ernault, Anais Amram, Daniel Arpin, Stéphanie Bertoli, Marta Busa, Tiffany Ceulemans, Berten Desir, Julie Doco-Fenzy, Martine Elalaoui, Siham Chafai Devriendt, Koenraad Faivre, Laurence Francannet, Christine Geneviève, David Gérard, Marion Gitiaux, Cyril Julia, Sophie Lebon, Sébastien Lubala, Toni Mathieu-Dramard, Michèle Maurey, Hélène Metreau, Julia Nasserereddine, Sanaa Nizon, Mathilde Pierquin, Geneviève Pouvreau, Nathalie Rivier-Ringenbach, Clothilde Rossi, Massimiliano Schaefer, Elise Sefiani, Abdelaziz Sigaudy, Sabine Sznajer, Yves[UCL] Tunca, Yusuf Guilmin Crepon, Sophie Alberti, Corinne Elmaleh-Bergès, Monique Benzacken, Brigitte Wollnick, Bernd Woods, C. Geoffrey Rauch, Anita Abramowicz, Marc El Ghouzzi, Vincent Gressens, Pierre Verloes, Alain Passemard, Sandrine (2018) Human Mutation — Vol. 39, no. 3, p. 319-332 (2018)
    • Article de périodique
    Clinical and Neurophysiologic Phenotypes in Neonates With Encephalopathy.
    Carapancea, Evelina[UCL] Cornet, Marie-Coralie Milh, Mathieu De Cosmo, Lucrezia Huang, Eric J Granata, Tiziana Striano, Pasquale Ceulemans, Berten Stein, Anja Morris-Rosendahl, Deborah Conti, Greta Mitra, Nipa Raymond, F Lucy Rowitch, David H Solazzi, Roberta Vercellino, Fabiana De Liso, Paola D'Onofrio, Gianluca Boniver, Clementina Danhaive, Olivier[UCL] Carkeek, Katherine[UCL] Salpietro, Vincenzo Weckhuysen, Sarah Fedrigo, Marny Angelini, Annalisa Castellotti, Barbara Lederer, Damien Benoit, Valerie Raviglione, Federico Guerrini, Renzo Dilena, Robertino Cilio, Maria-Roberta[UCL] (2023) Neurology — Vol. 100, no.12, p. e1234-e1247 (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)
    • Article de périodique
    Development of an electronic decision tool to support appropriate treatment choice in adult patients with epilepsy - Epi-Scope ®
    Legros, Benjamin Boon, Paul Ceulemans, Berten Coppens, Thomas Geens, Karine Hauman, Henri Lagae, Lieven Meurs, Alfred Mol, Leon Ossemann, Michel[UCL] Van Rijckevorsel, Germaine[UCL] Van Zandijcke, Michel Vrielynck, Pascal Wagemans, Daniëlla Grisar, Thierry (2012) Seizure - European Journal of Epilepsy — Vol. 21, no. 1, p. 32-39 (2012)