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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
2024 0

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217 results

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Page 1
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 Free article. 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.
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.
Fragile X syndrome and fragile XE mental retardation.
Sutherland GR, Mulley JC. Sutherland GR, et al. Among authors: mulley jc. Prenat Diagn. 1996 Dec;16(13):1199-211. doi: 10.1002/(SICI)1097-0223(199612)16:13<1199::AID-PD95>3.0.CO;2-T. Prenat Diagn. 1996. PMID: 9061751 Review.
217 results