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Alex Arzimanoglou
Alex Arzimanoglou
LYON
Verified email at chu-lyon.fr
Title
Cited by
Cited by
Year
ILAE official report: a practical clinical definition of epilepsy
RS Fisher, C Acevedo, A Arzimanoglou, A Bogacz, JH Cross, CE Elger, ...
Epilepsia 55 (4), 475-482, 2014
62922014
Definition of drug resistant epilepsy: consensus proposal by the ad hoc Task Force of the ILAE Commission on Therapeutic Strategies
P Kwan, A Arzimanoglou, AT Berg, MJ Brodie, W Allen Hauser, G Mathern, ...
Epilepsia 51 (6), 1069-1077, 2010
49002010
Is the underlying cause of epilepsy a major prognostic factor for recurrence?
F Semah, MC Picot, C Adam, D Broglin, A Arzimanoglou, B Bazin, ...
Neurology 51 (5), 1256-1262, 1998
13711998
Histopathological findings in brain tissue obtained during epilepsy surgery
I Blumcke, R Spreafico, G Haaker, R Coras, K Kobow, CG Bien, M Pfäfflin, ...
New England Journal of Medicine 377 (17), 1648-1656, 2017
7292017
Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology
A Arzimanoglou, J French, WT Blume, JH Cross, JP Ernst, M Feucht, ...
The Lancet Neurology 8 (1), 82-93, 2009
5412009
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction
G Lesca, G Rudolf, N Bruneau, N Lozovaya, A Labalme, N Boutry-Kryza, ...
Nature genetics 45 (9), 1061-1066, 2013
4752013
Treatment of pediatric epilepsy: European expert opinion, 2007
JW Wheless, DF Clarke, A Arzimanoglou, D Carpenter
Epileptic disorders 9 (4), 353-412, 2007
4542007
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
EL Heinzen, KJ Swoboda, Y Hitomi, F Gurrieri, S Nicole, B de Vries, ...
Nature genetics 44 (9), 1030-1034, 2012
4022012
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients
C Depienne, O Trouillard, C Saint-Martin, I Gourfinkel-An, D Bouteiller, ...
Journal of medical genetics 46 (3), 183-191, 2009
3932009
MECP2 mutations account for most cases of typical forms of Rett syndrome
T Bienvenu, A Carrié, N De Roux, MC Vinet, P Jonveaux, P Couvert, ...
Human molecular genetics 9 (9), 1377-1384, 2000
3482000
Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q
FV Elmslie, M Rees, MP Williamson, M Kerr, MJ Kjeldsen, K An Pang, ...
Human Molecular Genetics 6 (8), 1329-1334, 1997
3431997
Key clinical features to identify girls with CDKL5 mutations
N Bahi-Buisson, J Nectoux, H Rosas-Vargas, M Milh, N Boddaert, ...
Brain 131 (10), 2647-2661, 2008
3242008
Aicardi's epilepsy in children
A Arzimanoglou, R Guerrini, J Aicardi
(No Title), 2004
2922004
Nocturnal hypermotor seizures, suggesting frontal lobe epilepsy, can originate in the insula
P Ryvlin, L Minotti, G Demarquay, E Hirsch, A Arzimanoglou, D Hoffman, ...
Epilepsia 47 (4), 755-765, 2006
2842006
Vagus nerve stimulation for drug‐resistant epilepsy: a European long‐term study up to 24 months in 347 children
I Orosz, D McCormick, N Zamponi, S Varadkar, M Feucht, D Parain, ...
Epilepsia 55 (10), 1576-1584, 2014
2452014
Distinct neurological disorders with ATP1A3 mutations
EL Heinzen, A Arzimanoglou, A Brashear, SJ Clapcote, F Gurrieri, ...
The Lancet Neurology 13 (5), 503-514, 2014
2362014
Hypothalamic hamartoma and seizures: a treatable epileptic encephalopathy
SF Berkovic, A Arzimanoglou, R Kuzniecky, AS Harvey, A Palmini, ...
Epilepsia 44 (7), 969-973, 2003
2102003
Seizure outcome and use of antiepileptic drugs after epilepsy surgery according to histopathological diagnosis: a retrospective multicentre cohort study
HJ Lamberink, WM Otte, I Blümcke, KPJ Braun, M Aichholzer, I Amorim, ...
The Lancet Neurology 19 (9), 748-757, 2020
2042020
Epileptic encephalopathies of the Landau‐Kleffner and continuous spike and waves during slow‐wave sleep types: Genomic dissection makes the link with autism
G Lesca, G Rudolf, A Labalme, E Hirsch, A Arzimanoglou, P Genton, ...
Epilepsia 53 (9), 1526-1538, 2012
2002012
Greater response to placebo in children than in adults: a systematic review and meta-analysis in drug-resistant partial epilepsy
S Rheims, M Cucherat, A Arzimanoglou, P Ryvlin
PLoS medicine 5 (8), e166, 2008
1742008
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