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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2007 | 1 |
2008 | 2 |
2009 | 2 |
2011 | 1 |
2015 | 1 |
2016 | 1 |
2024 | 0 |
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Page 1
Epilepsy After Febrile Seizures: Twins Suggest Genetic Influence.
Pediatr Neurol. 2016 Feb;55:14-6. doi: 10.1016/j.pediatrneurol.2015.10.008. Epub 2015 Oct 31.
Pediatr Neurol. 2016.
PMID: 26638777
Free PMC article.
Importance of genetic factors in the occurrence of epilepsy syndrome type: a twin study.
Corey LA, Pellock JM, Kjeldsen MJ, Nakken KO.
Corey LA, et al.
Epilepsy Res. 2011 Nov;97(1-2):103-11. doi: 10.1016/j.eplepsyres.2011.07.018. Epub 2011 Aug 31.
Epilepsy Res. 2011.
PMID: 21885256
Free PMC article.
Item in Clipboard
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.
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.
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The accuracy of self-reported history of seizures in Danish, Norwegian and U.S. twins.
Corey LA, Kjeldsen MJ, Solaas MH, Nakken KO, Friis ML, Pellock JM.
Corey LA, et al.
Epilepsy Res. 2009 Mar;84(1):1-5. doi: 10.1016/j.eplepsyres.2008.11.014. Epub 2009 Jan 6.
Epilepsy Res. 2009.
PMID: 19128944
Free PMC article.
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SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.
Gilfillan GD, Selmer KK, Roxrud I, Smith R, Kyllerman M, Eiklid K, Kroken M, Mattingsdal M, Egeland T, Stenmark H, Sjøholm H, Server A, Samuelsson L, Christianson A, Tarpey P, Whibley A, Stratton MR, Futreal PA, Teague J, Edkins S, Gecz J, Turner G, Raymond FL, Schwartz C, Stevenson RE, Undlien DE, Strømme P.
Gilfillan GD, et al.
Am J Hum Genet. 2008 Apr;82(4):1003-10. doi: 10.1016/j.ajhg.2008.01.013. Epub 2008 Mar 13.
Am J Hum Genet. 2008.
PMID: 18342287
Free PMC article.
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Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.
Froyen G, Corbett M, Vandewalle J, Jarvela I, Lawrence O, Meldrum C, Bauters M, Govaerts K, Vandeleur L, Van Esch H, Chelly J, Sanlaville D, van Bokhoven H, Ropers HH, Laumonnier F, Ranieri E, Schwartz CE, Abidi F, Tarpey PS, Futreal PA, Whibley A, Raymond FL, Stratton MR, Fryns JP, Scott R, Peippo M, Sipponen M, Partington M, Mowat D, Field M, Hackett A, Marynen P, Turner G, Gécz J.
Froyen G, et al.
Am J Hum Genet. 2008 Feb;82(2):432-43. doi: 10.1016/j.ajhg.2007.11.002. Epub 2008 Jan 24.
Am J Hum Genet. 2008.
PMID: 18252223
Free PMC article.
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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.
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.
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