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Affichage: 6 résultats.
    • 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)
    • Communication
    Mutation of a putative potassium channel tetramerization domain in familial progressive myoclonic epilepsy
    Van Bogaert, Patrick Christiaens, Florence[UCL] Azizieh, Regis Aeby, Alec De Meirleir, Linda Desir, Julie Abramowicz, Marc J. (2006) 60th Annual Meeting of the American-Epilepsy-Society — San Diego (Ca)
    • Article de périodique
    Blue native polyacrylamide gel electrophoresis: A powerful tool in diagnosis of oxidative phosphorylation defects
    Van Coster, Rudy Smet, Joel George, Edith De Meirleir, Linda Seneca, Sara Van Hove, Johan Sebire, Guillaume[UCL] Verhelst, Helene De Bleecker, Jan Van Vlem, Bruno Verloo, Patrick Leroy, Jules (2001) Pediatric Research : international journal of human developmental biology — Vol. 50, no. 5, p. 658-665 (2001)
    • Article de périodique
    Analysis of the mitochondrial encoded subunits of complex 1 in 20 patients with a complex 1 deficiency
    Meulemans, Ann Lissens, Willy Van Coster, Rudy[UCL] De Meirleir, Linda Smet, Joél Nassogne, Marie-Cécile[UCL] Liebaers, Inge Seneca, Sara (2004) European Journal of Paediatric Neurology — Vol. 8, no. 6, p. 299-306 (2004)
    • Article de périodique
    Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformations.
    Stouffs, Katrien Moortgat, Stéphanie Vanderhasselt, Tim Vandervore, Laura Dica, Alice Mathot, Mikaël[UCL] Keymolen, Kathelijn Seneca, Sara Gheldof, Alexander De Meirleir, Linda Jansen, Anna C (2018) European journal of medical genetics — Vol. 61, no. 12, p. 733-737 (2018)
    • Article de périodique
    Mutation of a potassium channel-related gene in progressive myoclonic epilepsy.
    Van Bogaert, Patrick Azizieh, Regis Désir, Julie Aeby, Alec De Meirleir, Linda Laes, Jean-François Christiaens, Florence[UCL] Abramowicz, Marc-Joel (2007) Annals of Neurology — Vol. 61, no. 6, p. 579-586 (2007)