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Efficacy and tolerability of levetiracetam (LEV) as add-on treatment in refractory epileptic patients with partial onset seizures: Analysis of the crossover part of the European trial.

Bibliographic reference Shorvon, S. ; Otoul, C. ; Selak, I.. Efficacy and tolerability of levetiracetam (LEV) as add-on treatment in refractory epileptic patients with partial onset seizures: Analysis of the crossover part of the European trial..In: Epilepsia, Vol. 40, p. 248-249 (1999)
Permanent URL http://hdl.handle.net/2078.1/62275
  1. Li LM, J Neurol Neurosurg Psychiatry, 59, 384 (1995)
  2. Eksioğlu Y.Z., Scheffer I.E., Cardenas P., Knoll J., DiMario F., Ramsby G., Berg M., Kamuro K., Berkovic S.F., Duyk G.M., Parisi J., Huttenlocher P.R., Walsh C.A., Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development, 10.1016/s0896-6273(00)80025-2
  3. Brunelli Silvia, Faiella Antonio, Capra Valeria, Nigro Vincenzo, Simeone Antonio, Cama Armando, Boncinelli Edoardo, Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly, 10.1038/ng0196-94
  4. Reiner Orly, Carrozzo Romeo, Shen Ying, Wehnert Manfred, Faustinella Fabrizia, Dobyns William B., Caskey C. Thomas, Ledbetter David H., Isolation of a Miller–Dicker lissencephaly gene containing G protein β-subunit-like repeats, 10.1038/364717a0
  5. Portes Vincent des, Pinard Jean Marc, Billuart Pierre, Vinet Marie Claude, Koulakoff Annette, Carrié Alain, Gelot Antoinette, Dupuis Elisabeth, Motte Jacques, Berwald-Netter Yoheved, Catala Martin, Kahn Axel, Beldjord Cherif, Chelly Jamel, A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome, 10.1016/s0092-8674(00)80898-3
  6. Gleeson Joseph G, Allen Kristina M, Fox Jeremy W, Lamperti Edward D, Berkovic Samuel, Scheffer Ingrid, Cooper Edward C, Dobyns William B, Minnerath Sharon R, Ross M.Elizabeth, Walsh Christopher A, doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein, 10.1016/s0092-8674(00)80899-5
  7. Dobyns W. B., Guerrini R., Czapansky-Beilman D. K., Pierpont M.E.M., Breningstall G., Yock D. H., Bonanni P., Truwit C. L., Bilateral periventricular nodular heterotopia with mental retardation and syndactyly in boys: A new X-linked mental retardation syndrome, 10.1212/wnl.49.4.1042
  8. Fink JM, J Med Genet, 61, 379 (1997)
  9. Dobyns W. B., Andermann E., Andermann F., Czapansky-Beilman D., Dubeau F., Dulac O., Guerrini R., Hirsch B., Ledbetter D. H., Lee N. S., Motte J., Pinard J.-M., Radtke R. A., Ross M. E., Tampieri D., Walsh C. A., Truwit C. L., X-linked malformations of neuronal migration, 10.1212/wnl.47.2.331
  10. Sugama Seiichi, Kusano Kaoru, Monozygous twin with polymicrogyria and normal co-twin, 10.1016/0887-8994(94)90094-9
  11. Kuzniecky R, Epilepsia, 36, 1155 (1995)
  12. Costa T, J Med Genet, 34, 688 (1997)
  13. Boklage CE, Prog Clin Biol Res, 69, 155 (1981)
  14. Machin Geoffrey A., Some causes of genotypic and phenotypic discordance in monozygotic twin pairs, 10.1002/(sici)1096-8628(19960122)61:3<216::aid-ajmg5>3.0.co;2-s