Samuel F Berkovic
Samuel F Berkovic
Laureate Professor, University of Melbourne üzerinde doğrulanmış e-posta adresine sahip
Alıntı yapanlar
Alıntı yapanlar
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
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
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B
RH Wallace, DW Wang, R Singh, IE Scheffer, AL George, HA Phillips, ...
Nature genetics 19 (4), 366-370, 1998
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), 201-203, 1995
A potassium channel mutation in neonatal human epilepsy
C Biervert, BC Schroeder, C Kubisch, SF Berkovic, P Propping, ...
Science 279 (5349), 403-406, 1998
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
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
Mutant GABA A 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), 49-52, 2001
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
De novo mutations in epileptic encephalopathies
AS Allen, SF Berkovic, P Cossette, N Delanty, D Dlugos, EE Eichler, ...
Nature 501 (7466), 217-221, 2013
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
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
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
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
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
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
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
GL Carvill, SB Heavin, SC Yendle, JM McMahon, BJ O'Roak, J Cook, ...
Nature genetics 45 (7), 825-830, 2013
Prediction of seizure likelihood with a long-term, implanted seizure advisory system in patients with drug-resistant epilepsy: a first-in-man study
MJ Cook, TJ O'Brien, SF Berkovic, M Murphy, A Morokoff, G Fabinyi, ...
The Lancet Neurology 12 (6), 563-571, 2013
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
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
Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.
Makaleler 1–20