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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 1
1979 1
1980 3
1981 2
1982 6
1983 4
1984 1
1985 1
1986 1
1987 6
1988 11
1989 6
1990 5
1991 12
1992 9
1993 12
1994 6
1995 9
1996 8
1997 5
1998 6
1999 6
2000 4
2001 7
2002 7
2003 5
2004 10
2005 5
2006 8
2007 15
2008 9
2009 6
2010 8
2011 9
2012 5
2013 3
2014 2
2015 1
2016 1
2021 0
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217 results
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Page 1
KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
Weckhuysen S, Mandelstam S, Suls A, Audenaert D, Deconinck T, Claes LR, Deprez L, Smets K, Hristova D, Yordanova I, Jordanova A, Ceulemans B, Jansen A, Hasaerts D, Roelens F, Lagae L, Yendle S, Stanley T, Heron SE, Mulley JC, Berkovic SF, Scheffer IE, de Jonghe P. Weckhuysen S, et al. Among authors: mulley jc. Ann Neurol. 2012 Jan;71(1):15-25. doi: 10.1002/ana.22644. Ann Neurol. 2012. PMID: 22275249
Mutations in DEPDC5 cause familial focal epilepsy with variable foci.
Dibbens LM, de Vries B, Donatello S, Heron SE, Hodgson BL, Chintawar S, Crompton DE, Hughes JN, Bellows ST, Klein KM, Callenbach PM, Corbett MA, Gardner AE, Kivity S, Iona X, Regan BM, Weller CM, Crimmins D, O'Brien TJ, Guerrero-López R, Mulley JC, Dubeau F, Licchetta L, Bisulli F, Cossette P, Thomas PQ, Gecz J, Serratosa J, Brouwer OF, Andermann F, Andermann E, van den Maagdenberg AM, Pandolfo M, Berkovic SF, Scheffer IE. Dibbens LM, et al. Among authors: mulley jc. Nat Genet. 2013 May;45(5):546-51. doi: 10.1038/ng.2599. Epub 2013 Mar 31. Nat Genet. 2013. PMID: 23542697
The spectrum of SCN1A-related infantile epileptic encephalopathies.
Harkin LA, McMahon JM, Iona X, Dibbens L, Pelekanos JT, Zuberi SM, Sadleir LG, Andermann E, Gill D, Farrell K, Connolly M, Stanley T, Harbord M, Andermann F, Wang J, Batish SD, Jones JG, Seltzer WK, Gardner A; Infantile Epileptic Encephalopathy Referral Consortium, Sutherland G, Berkovic SF, Mulley JC, Scheffer IE. Harkin LA, et al. Among authors: mulley jc. Brain. 2007 Mar;130(Pt 3):843-52. doi: 10.1093/brain/awm002. Brain. 2007. PMID: 17347258
SCN1A mutations and epilepsy.
Mulley JC, Scheffer IE, Petrou S, Dibbens LM, Berkovic SF, Harkin LA. Mulley JC, et al. Hum Mutat. 2005 Jun;25(6):535-42. doi: 10.1002/humu.20178. Hum Mutat. 2005. PMID: 15880351 Review.
Epilepsy and the new cytogenetics.
Mulley JC, Mefford HC. Mulley JC, et al. Epilepsia. 2011 Mar;52(3):423-32. doi: 10.1111/j.1528-1167.2010.02932.x. Epub 2011 Jan 26. Epilepsia. 2011. PMID: 21269290 Free PMC article. Review.
Channelopathies in idiopathic epilepsy.
Heron SE, Scheffer IE, Berkovic SF, Dibbens LM, Mulley JC. Heron SE, et al. Among authors: mulley jc. Neurotherapeutics. 2007 Apr;4(2):295-304. doi: 10.1016/j.nurt.2007.01.009. Neurotherapeutics. 2007. PMID: 17395140 Review.
Susceptibility genes for complex epilepsy.
Mulley JC, Scheffer IE, Harkin LA, Berkovic SF, Dibbens LM. Mulley JC, et al. Hum Mol Genet. 2005 Oct 15;14 Spec No. 2:R243-9. doi: 10.1093/hmg/ddi355. Hum Mol Genet. 2005. PMID: 16244322 Review.
Genetic dissection of the common epilepsies.
Tan NC, Mulley JC, Scheffer IE. Tan NC, et al. Among authors: mulley jc. Curr Opin Neurol. 2006 Apr;19(2):157-63. doi: 10.1097/01.wco.0000218232.66054.46. Curr Opin Neurol. 2006. PMID: 16538090 Review.
Integrating maps of chromosome 16.
Mulley JC, Sutherland GR. Mulley JC, et al. Curr Opin Genet Dev. 1993 Jun;3(3):425-31. doi: 10.1016/0959-437x(93)90116-7. Curr Opin Genet Dev. 1993. PMID: 8353417 Review.
Human epilepsies: interaction of genetic and acquired factors.
Berkovic SF, Mulley JC, Scheffer IE, Petrou S. Berkovic SF, et al. Among authors: mulley jc. Trends Neurosci. 2006 Jul;29(7):391-397. doi: 10.1016/j.tins.2006.05.009. Trends Neurosci. 2006. PMID: 16769131 Review.
217 results
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