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Stéphane Auvin
Stéphane Auvin
Robert Debré University Hospital & INSERM U1141
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Cited by
Year
Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group
EH Kossoff, BA Zupec‐Kania, S Auvin, KR Ballaban‐Gil, ...
Epilepsia open 3 (2), 175-192, 2018
5362018
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
M Wolff, KM Johannesen, UBS Hedrich, S Masnada, G Rubboli, ...
Brain 140 (5), 1316-1336, 2017
5132017
High rate of recurrent de novo mutations in developmental and epileptic encephalopathies
FF Hamdan, CT Myers, P Cossette, P Lemay, D Spiegelman, AD Laporte, ...
The American Journal of Human Genetics 101 (5), 664-685, 2017
4002017
International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions
N Specchio, EC Wirrell, IE Scheffer, R Nabbout, K Riney, P Samia, ...
Epilepsia 63 (6), 1398-1442, 2022
3552022
ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions
SM Zuberi, E Wirrell, E Yozawitz, JM Wilmshurst, N Specchio, K Riney, ...
Epilepsia 63 (6), 1349-1397, 2022
3442022
Incidence, clinical presentation and location at diagnosis of pediatric inflammatory bowel disease: a prospective population-based study in northern France (1988-1999)
S Auvin, F Molinié, C Gower-Rousseau, F Brazier, V Merle, ...
Journal of pediatric gastroenterology and nutrition 41 (1), 49-55, 2005
2962005
ILAE definition of the idiopathic generalized epilepsy syndromes: position statement by the ILAE task force on nosology and definitions
E Hirsch, J French, IE Scheffer, A Bogacz, T Alsaadi, MR Sperling, ...
Epilepsia 63 (6), 1475-1499, 2022
2332022
MEF2C haploinsufficiency caused by either microdeletion of the 5q14. 3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and …
N Le Meur, M Holder-Espinasse, S Jaillard, A Goldenberg, S Joriot, ...
Journal of medical genetics 47 (1), 22-29, 2010
2332010
Fenfluramine for treatment-resistant seizures in patients with Dravet syndrome receiving stiripentol-inclusive regimens: a randomized clinical trial
R Nabbout, A Mistry, S Zuberi, N Villeneuve, A Gil-Nagel, ...
JAMA neurology 77 (3), 300-308, 2020
2092020
Ketogenic diet guidelines for infants with refractory epilepsy
E van der Louw, D van den Hurk, E Neal, B Leiendecker, G Fitzsimmon, ...
European Journal of Paediatric Neurology 20 (6), 798-809, 2016
1962016
Ketogenic diet exhibits anti‐inflammatory properties
N Dupuis, N Curatolo, JF Benoist, S Auvin
Epilepsia 56 (7), e95-e98, 2015
1942015
Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group
J Klepper, C Akman, M Armeno, S Auvin, M Cervenka, HJ Cross, ...
Epilepsia open 5 (3), 354-365, 2020
1712020
Expert opinion on the management of Lennox–Gastaut syndrome: treatment algorithms and practical considerations
JH Cross, S Auvin, M Falip, P Striano, A Arzimanoglou
Frontiers in neurology 8, 285292, 2017
1642017
Functional ultrasound imaging of brain activity in human newborns
C Demene, J Baranger, M Bernal, C Delanoe, S Auvin, V Biran, M Alison, ...
Science translational medicine 9 (411), eaah6756, 2017
1572017
Epilepsy in tuberous sclerosis complex: findings from the TOSCA Study
R Nabbout, E Belousova, MP Benedik, T Carter, V Cottin, P Curatolo, ...
Epilepsia open 4 (1), 73-84, 2019
1562019
Inflammation induced by LPS enhances epileptogenesis in immature rat and may be partially reversed by IL1RA
S Auvin, D Shin, A Mazarati, R Sankar
Epilepsia 51, 34-38, 2010
1492010
Polyunsaturated fatty acids and epilepsy
AY Taha, WMI Burnham, S Auvin
Epilepsia 51 (8), 1348-1358, 2010
1312010
Finding a better drug for epilepsy: antiepileptogenesis targets
K Kobow, S Auvin, F Jensen, W Löscher, I Mody, H Potschka, D Prince, ...
Epilepsia 53 (11), 1868-1876, 2012
1252012
International League Against Epilepsy classification and definition of epilepsy syndromes with onset at a variable age: position statement by the ILAE Task Force on Nosology …
K Riney, A Bogacz, E Somerville, E Hirsch, R Nabbout, IE Scheffer, ...
Epilepsia 63 (6), 1443-1474, 2022
1192022
Novel KCNQ2 and KCNQ3 Mutations in a Large Cohort of Families with Benign Neonatal Epilepsy: First Evidence for an Altered Channel Regulation by Syntaxin‐1A
MV Soldovieri, N Boutry‐Kryza, M Milh, D Doummar, B Heron, E Bourel, ...
Human mutation 35 (3), 356-367, 2014
1182014
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