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Rationale for treating epilepsy in children.
Guerrini R, Arzimanoglou A, Brouwer O. Guerrini R, et al. Epileptic Disord. 2002 Oct;4 Suppl 2:S9-21. Epileptic Disord. 2002. PMID: 12424080 Free article. Review.
Early-onset absence epilepsy and paroxysmal dyskinesia.
Guerrini R, Sanchez-Carpintero R, Deonna T, Santucci M, Bhatia KP, Moreno T, Parmeggiani L, Bernardina BD. Guerrini R, et al. Epilepsia. 2002 Oct;43(10):1224-9. doi: 10.1046/j.1528-1157.2002.13802.x. Epilepsia. 2002. PMID: 12366739 Free article.
Chromosomal disorders associated with epilepsy.
Battaglia A, Guerrini R. Battaglia A, et al. Among authors: guerrini r. Epileptic Disord. 2005 Sep;7(3):181-92. Epileptic Disord. 2005. PMID: 16162426 Free article. Review.
Epilepsy in children.
Guerrini R. Guerrini R. Lancet. 2006 Feb 11;367(9509):499-524. doi: 10.1016/S0140-6736(06)68182-8. Lancet. 2006. PMID: 16473127 Review.
Linkage and association analysis of CACNG3 in childhood absence epilepsy.
Everett KV, Chioza B, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dulac O, Eeg-Olofsson O, Feucht M, Friis M, Goutieres F, Guerrini R, Heils A, Kjeldsen M, Lehesjoki AE, Makoff A, Nabbout R, Olsson I, Sander T, Sirén A, McKeigue P, Robinson R, Taske N, Rees M, Gardiner M. Everett KV, et al. Among authors: guerrini r. Eur J Hum Genet. 2007 Apr;15(4):463-72. doi: 10.1038/sj.ejhg.5201783. Epub 2007 Jan 31. Eur J Hum Genet. 2007. PMID: 17264864 Free PMC article.
Genetics of epilepsy: epilepsy research foundation workshop report.
Sisodiya S, Cross JH, Blümcke I, Chadwick D, Craig J, Crino PB, Debenham P, Delanty N, Elmslie F, Gardiner M, Golden J, Goldstein D, Greenberg DA, Guerrini R, Hanna M, Harris J, Harrison P, Johnson MR, Kirov G, Kullman DM, Makoff A, Marini C, Nabbout R, Nashef L, Noebels JL, Ottman R, Pirmohamed M, Pitkänen A, Scheffer I, Shorvon S, Sills G, Wood N, Zuberi S. Sisodiya S, et al. Among authors: guerrini r. Epileptic Disord. 2007 Jun;9(2):194-236. doi: 10.1684/epd.2007.0107. Epileptic Disord. 2007. PMID: 17525034 Free article.
Linkage and mutational analysis of CLCN2 in childhood absence epilepsy.
Everett K, Chioza B, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dooley J, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis M, Guerrini R, Heils A, Kjeldsen M, Nabbout R, Sander T, Wirrell E, McKeigue P, Robinson R, Taske N, Gardiner M. Everett K, et al. Among authors: guerrini r. Epilepsy Res. 2007 Jul;75(2-3):145-53. doi: 10.1016/j.eplepsyres.2007.05.004. Epub 2007 Jun 18. Epilepsy Res. 2007. PMID: 17580110 Free article.
1,112 results