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Page 1
Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers.
Weckhuysen S, Holmgren P, Hendrickx R, Jansen AC, Hasaerts D, Dielman C, de Bellescize J, Boutry-Kryza N, Lesca G, Von Spiczak S, Helbig I, Gill D, Yendle S, Møller RS, Klitten L, Korff C, Godfraind C, Van Rijckevorsel K, De Jonghe P, Hjalgrim H, Scheffer IE, Suls A. Weckhuysen S, et al. Among authors: van rijckevorsel k. Epilepsia. 2013 May;54(5):e74-80. doi: 10.1111/epi.12124. Epub 2013 Feb 14. Epilepsia. 2013. PMID: 23409955 Free article.
Neuroserpin mutation causes electrical status epilepticus of slow-wave sleep.
Coutelier M, Andries S, Ghariani S, Dan B, Duyckaerts C, van Rijckevorsel K, Raftopoulos C, Deconinck N, Sonderegger P, Scaravilli F, Vikkula M, Godfraind C. Coutelier M, et al. Among authors: van rijckevorsel k. Neurology. 2008 Jul 1;71(1):64-6. doi: 10.1212/01.wnl.0000316306.08751.28. Neurology. 2008. PMID: 18591508 No abstract available.
Epileptic syndromes: differential treatment in infants, children, and adolescents.
Foulon M, Aeby A, Buzatu M, Christiaens F, de Borchgrave V, de Cocq C, de Tourtchaninoff M, Dubru JM, Ghariani S, Grisar T, Legros B, Lienard F, Ossemann M, Tugendhaft P, van Bogaert P, van Rijckevorsel K, Verheulpen D, Vrielynck P; Working group of francophone reference centres for refractory epilepsy. Foulon M, et al. Among authors: van rijckevorsel k, van bogaert p. Acta Neurol Belg. 2011 Sep;111(3):175-82. Acta Neurol Belg. 2011. PMID: 22141279 Review.
53 results