Kolexia
Nasser Hala
Pédiatrie
Hôpital Robert-Debré
Paris, France
37 Activités
0 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Microcéphalie Épilepsie Déficience intellectuelle Crises épileptiques Encéphalopathies Spasmes infantiles Maladies cochléaires Perte d'audition Ataxie

Industries

EXAFIELD
2 collaboration(s)
Dernière en 2022
UCB
2 collaboration(s)
Dernière en 2023
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Dernières activités

Real-life data comparing the efficacy of vigabatrin and oral steroids given sequentially or combined for infantile epileptic spasms syndrome.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society   27 novembre 2023
Focal epilepsy due to de novo SCN1A mutation.
Epileptic disorders : international epilepsy journal with videotape   31 janvier 2022
Subclinical maculopathy and retinopathy in transcobalamin deficiency: a 10-year follow-up.
Documenta ophthalmologica. Advances in ophthalmology   07 septembre 2021
EPHA7 haploinsufficiency is associated with a neurodevelopmental disorder.
Clinical genetics   01 juillet 2021
Severe Phenotype in Patients with Large Deletions of .
Cancers   13 juin 2021
Evolution of the retinal function by flash-ERG in one child suffering from neuronal ceroid lipofuscinosis CLN2 treated with cerliponase alpha: case report.
Documenta ophthalmologica. Advances in ophthalmology   06 mai 2021
Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesia.
European journal of human genetics : EJHG   28 mai 2020
primary microcephaly is associated with hypothalamic, retinal and cochlear developmental defects.
Journal of medical genetics   03 février 2020
Felbamate for infantile spasms syndrome resistant to first-line treatments.
Developmental medicine and child neurology   18 décembre 2019
Paediatric-onset neuronal ceroid lipofuscinosis: first symptoms and presentation at diagnosis.
Developmental medicine and child neurology   05 septembre 2019