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Results 1-10 of 36 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2003
Channelopathies as a genetic cause of epilepsy
Mulley, J.
;
Scheffer, I.
;
Petrou, S.
;
Berkovic, S.
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.
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.
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.
2004
Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathy
Berkovic, S.
;
Heron, S.
;
Giordano, L.
;
Marini, C.
;
Guerrini, R.
;
Kaplan, R.
;
Gambardella, A.
;
Steinlein, O.
;
Grinton, B.
;
Dean, J.
;
Bordo, L.
;
Hodgson, B.
;
Yamamoto, T.
;
Mulley, J.
;
Zara, F.
;
Scheffer, I.
2003
X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3
Gedeon, A.
;
Nelson, J.
;
Gecz, J.
;
Mulley, J.
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.
2004
Genetic association studies in epilepsy: The truth is out there
Tan, N.
;
Mulley, J.
;
Berkovic, S.
2000
Genes for cognitive function: Developments on the X
Gecz, J.
;
Mulley, J.
Discover
Author
29
Berkovic, S.
27
Scheffer, I.
10
Dibbens, L.
9
Harkin, L.
9
Heron, S.
8
Wallace, R.
7
Petrou, S.
6
Gecz, J.
4
Gedeon, A.
4
Grinton, B.
.
next >
Subject
9
Adolescent
9
Molecular Sequence Data
8
Epilepsy
8
Genetic Predisposition to Disease
8
Middle Aged
8
NAV1.1 Voltage-Gated Sodium Channel
7
Amino Acid Sequence
7
Animals
7
Child, Preschool
7
Infant
.
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Date issued
2
2010 - 2011
34
2000 - 2009