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389 results

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Page 1
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: dulac o. 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.
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: dulac o. 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.
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14.
Chioza BA, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dooley JM, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis ML, Guerrini R, Kjeldsen MJ, Nabbout R, Nashef L, Sander T, Sirén A, Wirrell E, McKeigue P, Robinson R, Gardiner RM, Everett KV. Chioza BA, et al. Among authors: dulac o. Epilepsy Res. 2009 Dec;87(2-3):247-55. doi: 10.1016/j.eplepsyres.2009.09.010. Epub 2009 Oct 17. Epilepsy Res. 2009. PMID: 19837565 Free PMC article.
Evaluation of CACNA1H in European patients with childhood absence epilepsy.
Chioza B, Everett K, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis M, Heils A, Kjeldsen M, Larsson K, Lehesjoki AE, Nabbout R, Olsson I, Sander T, Sirén A, Robinson R, Rees M, Gardiner RM. Chioza B, et al. Among authors: dulac o. Epilepsy Res. 2006 May;69(2):177-81. doi: 10.1016/j.eplepsyres.2006.01.009. Epub 2006 Feb 28. Epilepsy Res. 2006. PMID: 16504478 Free article.
Epileptic syndromes in infancy and childhood.
Nabbout R, Dulac O. Nabbout R, et al. Among authors: dulac o. Curr Opin Neurol. 2008 Apr;21(2):161-6. doi: 10.1097/WCO.0b013e3282f7007e. Curr Opin Neurol. 2008. PMID: 18317274 Review.
Exploration of the genetic architecture of idiopathic generalized epilepsies.
Hempelmann A, Taylor KP, Heils A, Lorenz S, Prud'homme JF, Nabbout R, Dulac O, Rudolf G, Zara F, Bianchi A, Robinson R, Gardiner RM, Covanis A, Lindhout D, Stephani U, Elger CE, Weber YG, Lerche H, Nürnberg P, Kron KL, Scheffer IE, Mulley JC, Berkovic SF, Sander T. Hempelmann A, et al. Among authors: dulac o. Epilepsia. 2006 Oct;47(10):1682-90. doi: 10.1111/j.1528-1167.2006.00677.x. Epilepsia. 2006. PMID: 17054691 Free article.
Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12.
Sander T, Windemuth C, Schulz H, Saar K, Gennaro E, Riggio C, Bianchi A, Zara F, Rudolf G, Picard F, Bulteau C, Kaminska A, Cieuta C, Prud'homme JF, Dulac O, Bate L, Robinson R, Gardiner RM, Covanis A, de Haan GJ, Janssen GA, van Erp MG, Boezeman EH, Lindhout D, Heils A, Nürnberg P, Janz D; European Consortium on the Genetics of Idiopathic Generalized Epilepsy. Sander T, et al. Among authors: dulac o. Epilepsia. 2003 Jan;44(1):32-9. doi: 10.1046/j.1528-1157.2003.51501.x. Epilepsia. 2003. PMID: 12581227 Free article.
A gene for pyridoxine-dependent epilepsy maps to chromosome 5q31.
Cormier-Daire V, Dagoneau N, Nabbout R, Burglen L, Penet C, Soufflet C, Desguerre I, Munnich A, Dulac O. Cormier-Daire V, et al. Among authors: dulac o. Am J Hum Genet. 2000 Oct;67(4):991-3. doi: 10.1086/303087. Epub 2000 Sep 7. Am J Hum Genet. 2000. PMID: 10978228 Free PMC article.
Epileptic encephalopathies: a brief overview.
Nabbout R, Dulac O. Nabbout R, et al. Among authors: dulac o. J Clin Neurophysiol. 2003 Nov-Dec;20(6):393-7. doi: 10.1097/00004691-200311000-00002. J Clin Neurophysiol. 2003. PMID: 14734929 Review.
389 results