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Results 11-17 of 17 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2008
Human nocturnal frontal lobe epilepsy: Pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor β-subunit mutations outside the ion channel pore
Hoda, J.
;
Gu, W.
;
Friedli, M.
;
Phillips, H.
;
Bertrand, S.
;
Antonarakis, S.
;
Goudie, D.
;
Roberts, R.
;
Scheffer, I.
;
Marini, C.
;
Patel, J.
;
Berkovic, S.
;
Mulley, J.
;
Steinlein, O.
;
Bertrand, D.
2010
De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin
Heron, S.
;
Scheffer, I.
;
Iona, X.
;
Zuberi, S.
;
Birch, R.
;
McMahon, J.
;
Bruce, C.
;
Berkovic, S.
;
Mulley, J.
2007
NEDD4-2 as a potential candidate susceptibility gene for epileptic photosensitivity
Dibbens, L.
;
Ekberg, J.
;
Taylor, I.
;
Hodgson, B.
;
Conroy, S.
;
Lensink, I.
;
Kumar, S.
;
Zielinski, M.
;
Harkin, L.
;
Sutherland, G.
;
Adams, D.
;
Berkovic, S.
;
Scheffer, I.
;
Mulley, J.
;
Poronnik, P.
2011
De novo SCN1A mutations in migrating partial seizures of infancy
Carranza Rojo, D.
;
Hamiwka, L.
;
McMahon, J.
;
Dibbens, L.
;
Arsov, T.
;
Suls, A.
;
Stodberg, T.
;
Kelley, K.
;
Wirrell, E.
;
Appleton, B.
;
Mackay, M.
;
Freeman, J.
;
Yendle, S.
;
Berkovic, S.
;
Bienvenu, T.
;
De Jonghe, P.
;
Thorburn, D.
;
Mulley, J.
;
Mefford, H.
;
Scheffer, I.
2004
LGI1 mutations in temporal lobe epilepsies
Berkovic, S.
;
Izzillo, P.
;
McMahon, J.
;
Harkin, L.
;
McIntosh, A.
;
Phillips, H.
;
Briellmann, R.
;
Wallace, R.
;
Mazarib, A.
;
Neufeld, M.
;
Korczyn, A.
;
Scheffer, I.
;
Mulley, J.
2002
Generalized epilepsy with febrile seizures plus: Mutation of the sodium channel subunit SCN1B
Wallace, R.
;
Scheffer, I.
;
Parasivam, G.
;
Barnett, S.
;
Wallace, G.
;
Sutherland, G.
;
Berkovic, S.
;
Mulley, J.
2009
SCARB2 Mutations in Progressive Myoclonus Epilepsy (PME) Without Renal Failure
Dibbens, L.
;
Michelucci, R.
;
Gambardella, A.
;
Andermann, F.
;
Rubboli, G.
;
Bayly, M.
;
Joensuu, T.
;
Vears, D.
;
Franceschetti, S.
;
Canafoglia, L.
;
Wallace, R.
;
Bassuk, A.
;
Power, D.
;
Tassinari, C.
;
Andermann, E.
;
Lehesjoki, A.
;
Berkovic, S.
Discover
Author
15
Scheffer, I.
14
Mulley, J.
8
Dibbens, L.
6
Wallace, R.
5
Harkin, L.
5
Phillips, H.
5
Sutherland, G.
4
McMahon, J.
3
Hodgson, B.
2
Bayly, M.
.
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Subject
17
Female
17
Humans
11
Pedigree
8
Mutation
7
Adult
6
Epilepsy, Generalized
6
Sodium Channels
5
Child
5
Genetic Linkage
5
Genetic Predisposition to Disease
.
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Date issued
4
2010 - 2014
10
2000 - 2009
3
1995 - 1999