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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
Fragile X Syndrome and other causes of X-Linked mental handicap
Sutherland, G.
;
Gecz, J.
;
Mulley, J.
;
Rimoin, D.
;
Connor, J.
;
Emery, A.
;
Pyeritz, R.
;
Korf, B.
2008
Forty years from markers to genes
Mulley, J.
2002
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype
Cundy, T.
;
Hegde, M.
;
Naot, D.
;
Chong, B.
;
King, A.
;
Wallace, R.
;
Mulley, J.
;
Love, D.
;
Seidel, J.
;
Fawkner, M.
;
Banovic, T.
;
Callon, K.
;
Grey, A.
;
Reid, I.
;
Middleton-Hardie, C.
;
Cornish, J.
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.
2005
SCN1A mutations and epiliepsy
Mulley, J.
;
Scheffer, I.
;
Petrou, S.
;
Dibbens, L.
;
Berkovic, S.
;
Harkin, L.
Discover
Author
39
Berkovic, S.
35
Scheffer, I.
13
Dibbens, L.
12
Heron, S.
11
Harkin, L.
11
Wallace, R.
10
Petrou, S.
7
Gecz, J.
6
Grinton, B.
6
Phillips, H.
.
next >
Subject
10
Epilepsy
9
Adolescent
9
Genetic Predisposition to Disease
9
Molecular Sequence Data
8
Animals
8
Middle Aged
8
Mutation, Missense
8
NAV1.1 Voltage-Gated Sodium Channel
8
Phenotype
7
Amino Acid Sequence
.
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Date issued
4
2010 - 2011
46
2000 - 2009