Samuel F Berkovic
Samuel F Berkovic
Professor of Medicine (Neurology)
Verified email at unimelb.edu.au
TitleCited byYear
Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005–2009
AT Berg, SF Berkovic, MJ Brodie, J Buchhalter, JH Cross, ...
Epilepsia 51 (4), 676-685, 2010
37832010
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ▀1 subunit gene SCN1B
RH Wallace, DW Wang, R Singh, IE Scheffer, AL George Jr, HA Phillips, ...
Nature genetics 19 (4), 366, 1998
12081998
A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
OK Steinlein, JC Mulley, P Propping, RH Wallace, HA Phillips, ...
Nature genetics 11 (2), 201, 1995
11271995
A potassium channel mutation in neonatal human epilepsy
C Biervert, BC Schroeder, C Kubisch, SF Berkovic, P Propping, ...
Science 279 (5349), 403-406, 1998
10991998
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein
JG Gleeson, KM Allen, JW Fox, ED Lamperti, S Berkovic, I Scheffer, ...
Cell 92 (1), 63-72, 1998
9841998
Mutant GABAA receptor γ2-subunit in childhood absence epilepsy and febrile seizures
RH Wallace, C Marini, S Petrou, LA Harkin, DN Bowser, RG Panchal, ...
Nature genetics 28 (1), 49, 2001
8562001
Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes.
IE Scheffer, SF Berkovic
Brain: a journal of neurology 120 (3), 479-490, 1997
8541997
Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia
JW Fox, ED Lamperti, YZ Ekşioğlu, SE Hong, Y Feng, DA Graham, ...
Neuron 21 (6), 1315-1325, 1998
7931998
ILAE classification of the epilepsies: position paper of the ILAE Commission for Classification and Terminology
IE Scheffer, S Berkovic, G Capovilla, MB Connolly, J French, L Guilhoto, ...
Epilepsia 58 (4), 512-521, 2017
6662017
Autosomal dominant nocturnal frontal lobe epilepsy: a distinctive clinical disorder
IE Scheffer, KP Bhatia, I Lopes-Cendes, DR Fish, CD Marsden, ...
Brain 118 (1), 61-73, 1995
5981995
De novo mutations in epileptic encephalopathies
AS Allen, SF Berkovic, P Cossette, N Delanty, D Dlugos, EE Eichler, ...
Nature 501 (7466), 217, 2013
5912013
Epileptology of the first-seizure presentation: a clinical, electroencephalographic, and magnetic resonance imaging study of 300 consecutive patients
MA King, MR Newton, GD Jackson, GJ Fitt, LA Mitchell, MJ Silvapulle, ...
The Lancet 352 (9133), 1007-1011, 1998
5901998
Preoperative MRI predicts outcome of temporal lobectomy: an actuarial analysis
SF Berkovic, AM McIntosh, RM Kalnins, GD Jackson, GCA Fabinyi, ...
Neurology 45 (7), 1358-1363, 1995
5371995
Truncation of the GABAA-receptor γ2 subunit in a family with generalized epilepsy with febrile seizures plus
LA Harkin, DN Bowser, LM Dibbens, R Singh, F Phillips, RH Wallace, ...
The American Journal of Human Genetics 70 (2), 530-536, 2002
5092002
Hippocampal sclerosis can be reliably detected by magnetic resonance imaging
GD Jackson, SF Berkovic, BM Tress, RM Kalnins, GCA Fabinyi, PF Bladin
Neurology 40 (12), 1869-1869, 1990
5081990
Temporal lobectomy: long-term seizure outcome, late recurrence and risks for seizure recurrence
AM McIntosh, RM Kalnins, LA Mitchell, GCA Fabinyi, RS Briellmann, ...
Brain 127 (9), 2018-2030, 2004
4402004
Epilepsies in twins: genetics of the major epilepsy syndromes
SF Berkovic, RA Howell, DA Hay, JL Hopper
Annals of neurology 43 (4), 435-445, 1998
437*1998
Hippocampal sclerosis in temporal lobe epilepsy demonstrated by magnetic resonance imaging
SF Berkovic, F Andermann, A Olivier, R Ethier, D Melanson, Y Robitaille, ...
Annals of Neurology: Official Journal of the American Neurologicalá…, 1991
4311991
The spectrum of SCN1A-related infantile epileptic encephalopathies
LA Harkin, JM McMahon, X Iona, L Dibbens, JT Pelekanos, SM Zuberi, ...
Brain 130 (3), 843-852, 2007
4202007
An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy
OK Steinlein, A Magnusson, J Stoodt, S Bertrand, S Weiland, SF Berkovic, ...
Human Molecular Genetics 6 (6), 943-947, 1997
4091997
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