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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
Results by year
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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
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.
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.
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.
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.
Channelopathies as a genetic cause of epilepsy.
Mulley JC, Scheffer IE, Petrou S, Berkovic SF. Mulley JC, et al. Curr Opin Neurol. 2003 Apr;16(2):171-6. doi: 10.1097/01.wco.0000063767.15877.c7. Curr Opin Neurol. 2003. PMID: 12644745 Review.
217 results
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