Kolexia
Boddaert Nathalie
Radio-diagnostic
Hôpital Necker Enfants Malades
Paris, France
498 Activités
172 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Gliome Tumeurs du cerveau Déficience intellectuelle Maladies mitochondriales Épilepsie Gliome infiltrant du tronc cérébral Microcéphalie Encéphalopathies Atrophie

Industries

Guerbet
1 collaboration(s)
Dernière en 2018
Shire
1 collaboration(s)
Dernière en 2018
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Dernières activités

Vitamin deficiencies in children: Lessons from clinical and neuroimaging findings
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society   26 février 2024
De novo variants in DENND5B cause a neurodevelopmental disorder.
American journal of human genetics   21 février 2024
CNS erythroblastic sarcoma: a potential emerging pediatric tumor type characterized by NFIA::RUNX1T1/3 fusions.
Acta neuropathologica communications   19 janvier 2024
"Hemispheric pilocytic astrocytoma" revisited: A comprehensive clinicopathological and molecular series emphasizing their overlap with other glioneuronal tumors.
Journal of neuropathology and experimental neurology   17 janvier 2024
CREIM: Mapping Epileptic Networks Using Multimodal Imaging
Essai Clinique (Imagine Institute)   02 janvier 2024
Dandelion sign, a highly specific neuroradiological feature for the diagnosis of EBF3-related neurodevelopmental disorder?
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
De novo variants in DENND5B perturb intracellular vesicular trafficking and cause neurodevelopmental disorders with epilepsy and white matter abnormalities
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
A Phase II double-blind multi-center, placebo-controlled trial, to assess the efficacy and safety of alpelisib (BYL719) in pediatric and adult patients with Megalencephaly-CApillary malformation Polymicrogyria syndrome (MCAP): the SESAM trial
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
Le syndrome Axenfeld-Rieger
HAS Publications   21 décembre 2023
Fluid suppression in amide proton transfer-weighted (APTw) CEST imaging: New theoretical insights and clinical benefits.
Magnetic resonance in medicine   10 décembre 2023