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Results 1-10 of 13 (Search time: 0.002 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)
2005
SCN1A mutations and epiliepsy
Mulley, J.
;
Scheffer, I.
;
Petrou, S.
;
Dibbens, L.
;
Berkovic, S.
;
Harkin, L.
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.
2005
Susceptibility genes for complex epilepsy
Mulley, J.
;
Scheffer, I.
;
Harkin, L.
;
Berkovic, S.
;
Dibbens, L.
2001
Neuronal sodium-channel a1-subunit mutations in generalized epilepsy with febrile seizures plus
Wallace, R.
;
Scheffer, I.
;
Barnett, S.
;
Richards, M.
;
Dibbens, L.
;
Desai, R.
;
Lerman-Sagie, T.
;
Lev, D.
;
Mazarib, A.
;
Brand, N.
;
Ben-Zeev, B.
;
Goikhman, I.
;
Singh, R.
;
Kremmidiotis, G.
;
Gardner, A.
;
Sutherland, G.
;
George Jr., A.
;
Mulley, J.
;
Berkovic, S.
2007
Channelopathies in idiopathic epilepsy
Heron, S.
;
Scheffer, I.
;
Berkovic, S.
;
Dibbens, L.
;
Mulley, J.
2007
Is photosensitive epilepsy less common in males due to variation in X chromosome photopigment genes?
Taylor, I.
;
Hodgson, B.
;
Scheffer, I.
;
Mulley, J.
;
Berkovic, S.
;
Dibbens, L.
Discover
Author
11
Scheffer, I.
6
Harkin, L.
4
Petrou, S.
4
Wallace, R.
2
Gardner, A.
2
Grinton, B.
2
Hodgson, B.
2
Jackson, G.
2
McMahon, J.
2
Richards, M.
.
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Subject
10
Humans
6
Male
6
Sodium Channels
5
Female
5
Nerve Tissue Proteins
4
Animals
4
Molecular Sequence Data
4
NAV1.1 Voltage-Gated Sodium Channel
4
Pedigree
3
Amino Acid Sequence
.
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Date issued
2
2010
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2005
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2003
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2001