Kolexia
Ilea Adina
Pédiatrie
Hôpitaux de Saint-Maurice
Saint-Maurice, France
23 Activités
0 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Épilepsie Crises épileptiques Encéphalopathies Spasme Spasmes infantiles Syndrome de Lennox-Gastaut Épilepsies partielles Myoclonie Tyrosinémies

Industries

Ipsen
1 collaboration(s)
Dernière en 2023
Abbvie
1 collaboration(s)
Dernière en 2023
Adept Field Solutions
1 collaboration(s)
Dernière en 2020
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{{person.topindus4.tot}} collaboration(s)
Dernière en {{person.topindus4.last}}

Dernières activités

Focal epilepsy due to de novo SCN1A mutation.
Epileptic disorders : international epilepsy journal with videotape   31 janvier 2022
COGNIBENZO: Cognitive Impact of Benzodiazepin Withdrawn After Curative Epilepsy Surgery in Children With Focal Epilepsy
Essai Clinique (Assistance publique – Hôpitaux de Paris)   23 mars 2021
Felbamate for infantile spasms syndrome resistant to first-line treatments.
Developmental medicine and child neurology   18 décembre 2019
The epileptology of GNB5 encephalopathy.
Epilepsia   20 octobre 2019
Paediatric-onset neuronal ceroid lipofuscinosis: first symptoms and presentation at diagnosis.
Developmental medicine and child neurology   05 septembre 2019
Early identification of epileptic encephalopathy with continuous spikes-and-waves during sleep: A case-control study.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society   27 avril 2018
Myoclonic jerks are commonly associated with absence seizures in early-onset absence epilepsy.
Epileptic disorders : international epilepsy journal with videotape   06 avril 2018
Use of perampanel in children and adolescents with Lennox-Gastaut Syndrome.
Epilepsy & behavior : E&B   14 juillet 2017
Use of modified Atkins diet in glucose transporter type 1 deficiency syndrome.
Developmental medicine and child neurology   08 juin 2016
An unfortunate challenge: Ketogenic diet for the treatment of Lennox-Gastaut syndrome in tyrosinemia type 1.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society   16 mars 2016