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Issue Date
Title
Author(s)
2004
Familial partial epilepsy with variable foci: Clinical features and linkage to chromosome 22q12
Berkovic, S.
;
Serratosa, J.
;
Phillips, H.
;
Xiong, L.
;
Andermann, E.
;
Diaz-Otero, F.
;
Gomez-Garre, P.
;
Martin, M.
;
Fernandez-Bullido, Y.
;
Andermann, F.
;
Lopes-Cendes, I.
;
Dubeau, F.
;
Desbiens, R.
;
Scheffer, I.
;
Wallace, R.
;
Mulley, J.
;
Pandolfo, M.
2003
Channelopathies as a genetic cause of epilepsy
Mulley, J.
;
Scheffer, I.
;
Petrou, S.
;
Berkovic, 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.
2002
Sodium-channel defects in benign familial neonatal-infantile seizures
Heron, S.
;
Crossland, K.
;
Andermann, E.
;
Phillips, H.
;
Hall, A.
;
Bleasel, A.
;
Shevell, M.
;
Mercho, S.
;
Seni, M.
;
Guiot, M.
;
Mulley, J.
;
Berkovic, S.
;
Scheffer, I.
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)
2000
A de novo mutation in sporadic nocturnal frontal lobe epilepsy
Phillips, H.
;
Marini, C.
;
Scheffer, I.
;
Sutherland, G.
;
Mulley, J.
;
Berkovic, S.
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.
Discover
Author
39
Mulley, J.
36
Scheffer, I.
17
Dibbens, L.
12
Heron, S.
11
Harkin, L.
10
Petrou, S.
9
Wallace, R.
6
Grinton, B.
6
McMahon, J.
6
Phillips, H.
.
next >
Subject
9
Epilepsy
8
Adolescent
8
Genetic Predisposition to Disease
8
NAV1.1 Voltage-Gated Sodium Channel
8
Phenotype
7
Gene Frequency
7
Genotype
7
Infant
6
Middle Aged
6
Molecular Sequence Data
.
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Date issued
7
2010 - 2016
36
2000 - 2009