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Results 1-10 of 17 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2007
Reduced cortical inhibition in a mouse model of familial childhood absence epilepsy
Tan, H.
;
Reid, C.
;
Single, F.
;
Davies, P.
;
Chiu, C.
;
Murphy, S.
;
Clarke, A.
;
Dibbens, L.
;
Krestel, H.
;
Mulley, J.
;
Jones, M.
;
Seeburg, P.
;
Sakmann, B.
;
Berkovic, S.
;
Sprengel, R.
;
Petrou, S.
2007
What is the role of genetics in epilepsy?
Scheffer, I.
;
Dibbens, L.
;
Berkovic, S.
;
Mulley, J.
;
Sanjay Sisodiya,
;
Epilepsy Research Foundation workshop (6th : 2006 : Oxford, UK)
2013
Do mutations in SCN1B cause Dravet syndrome?
Kim, Y.
;
Dibbens, L.
;
Marini, C.
;
Suls, A.
;
Chemaly, N.
;
Mei, D.
;
McMahon, J.
;
Iona, X.
;
Berkovic, S.
;
De Jonghe, P.
;
Guerrini, R.
;
Nabbout, R.
;
Scheffer, I.
2014
Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive decline
Kim, Y.
;
Bellows, S.
;
Mcmahon, J.
;
Iona, X.
;
Damiano, J.
;
Dibbens, L.
;
Kelley, K.
;
Gill, D.
;
Cross, J.
;
Berkovic, S.
;
Scheffer, I.
2005
SCN1A mutations and epiliepsy
Mulley, J.
;
Scheffer, I.
;
Petrou, S.
;
Dibbens, L.
;
Berkovic, S.
;
Harkin, L.
2016
Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy
Bagnall, R.
;
Crompton, D.
;
Petrovski, S.
;
Lam, L.
;
Cutmore, C.
;
Garry, S.
;
Sadleir, L.
;
Dibbens, L.
;
Cairns, A.
;
Kivity, S.
;
Afawi, Z.
;
Regan, B.
;
Duflou, J.
;
Berkovic, S.
;
Scheffer, I.
;
Semsarian, C.
2011
A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia
Corbett, M.
;
Schwake, M.
;
Bahlo, M.
;
Dibbens, L.
;
Lin, M.
;
Gandolfo, L.
;
Vears, D.
;
O'Sullivan, J.
;
Robertson, T.
;
Bayly, M.
;
Gardner, A.
;
Vlaar, A.
;
Korenke, G.
;
Bloem, B.
;
de Coo, I.
;
Verhagen, J.
;
Lehesjoki, A.
;
Gecz, J.
;
Berkovic, S.
2010
A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24
Bahlo, M.
;
Jolly, L.
;
Afawi, Z.
;
Gardner, A.
;
Oliver, K.
;
Tan, S.
;
Coffey, A.
;
Mulley, J.
;
Dibbens, L.
;
Simri, W.
;
Shalata, A.
;
Kivity, S.
;
Jackson, G.
;
Berkovic, S.
;
Gecz, J.
;
Corbett, M.
2007
Temporal lobe epilepsy and GEFS(+) phenotypes associated with SCN1B mutations
Scheffer, I.
;
Harkin, L.
;
Grinton, B.
;
Dibbens, L.
;
Turner, S.
;
Zielinski, M.
;
Xu, R.
;
Jackson, G.
;
Adams, J.
;
Connellan, M.
;
Petrou, S.
;
Wellard, R.
;
Briellmann, R.
;
Wallace, R.
;
Mulley, J.
;
Berkovic, S.
2002
Truncation of the GABAA-receptor γ2 subunit in a family with generalized epilepsy with febrile seizures plus
Harkin, L.
;
Bowser, D.
;
Dibbens, L.
;
Singh, R.
;
Phillips, F.
;
Wallace, R.
;
Richards, M.
;
Williams, D.
;
Mulley, J.
;
Berkovic, S.
;
Scheffer, I.
;
Petrou, S.
Discover
Author
14
Scheffer, I.
13
Mulley, J.
6
Harkin, L.
4
Petrou, S.
4
Wallace, R.
3
Gardner, A.
3
Iona, X.
3
McMahon, J.
2
Afawi, Z.
2
Bahlo, M.
.
next >
Subject
11
Humans
7
Male
6
Female
6
Sodium Channels
5
Molecular Sequence Data
5
Nerve Tissue Proteins
5
Pedigree
4
Amino Acid Sequence
4
Animals
4
Mutation
.
next >
Date issued
6
2010 - 2016
11
2001 - 2009