Kolexia
Bahi Nadia Pédiatrie
Bahi Nadia
Pédiatrie
Hôpital Necker Enfants Malades
Paris, France
211 Activités
0 Followers
Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Épilepsie Microcéphalie Malformations corticales Déficience intellectuelle Syndrome de Rett Polymicrogyrie Crises épileptiques Encéphalopathies Lissencéphalie

Collaborateurs

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Boddaert Nathalie
Boddaert Nathalie
Hôpital Necker Enfants Malades, Paris, France
Desguerre Isabelle
Desguerre Isabelle
Hôpital Necker Enfants Malades, Paris, France
Bienvenu Thierry
Bienvenu Thierry
Hôpital Cochin, Paris, France
Auvin Stephane
Auvin Stephane
Hôpital Robert-Debré, Paris, France

Industries

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B3TSI
8 collaboration(s)
Dernière en 2023
P\S\L Group Services
8 collaboration(s)
Dernière en 2021
Schlesinger Group France
7 collaboration(s)
Dernière en 2023
Adept Field Solutions
6 collaboration(s)
Dernière en 2023

Dernières activités

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Long-term treatment with ganaxolone for seizures associated with cyclin-dependent kinase-like 5 deficiency disorder: Two-year open-label extension follow-up.
Epilepsia   10 novembre 2023
Genetic Primary Microcephalies: When Centrosome Dysfunction Dictates Brain and Body Size.
Cells   07 juillet 2023
Marigold: A Double-blind, Randomized, Placebo-controlled Trial of Adjunctive Ganaxolone Treatment in Children and Young Adults With Cyclin-dependent Kinase-like 5 (CDKL5) Deficiency Disorder (CDD) Followed by Long-term Open-label Treatment
Essai Clinique (Marinus Pharmaceuticals)   12 avril 2023
A human dynein heavy chain mutation impacts cortical progenitor cells causing developmental defects, reduced brain size and altered brain architecture.
Neurobiology of disease   16 mars 2023
Activation of the PI3K/AKT/mTOR Pathway in Cajal-Retzius Cells Leads to Their Survival and Increases Susceptibility to Kainate-Induced Seizures.
International journal of molecular sciences   11 mars 2023
Neurology Session: Characteristics of FOXG1 ( Movement) - Dr. Nadia Bahi- Buisson
Youtube @ FOXG1 Research Foundation   01 janvier 2023
Délétion 1p36
HAS Publications   09 septembre 2022
Tubulin mutations in human neurodevelopmental disorders.
Seminars in cell & developmental biology   30 juillet 2022
International Consensus Recommendations for the Assessment and Management of Individuals With CDKL5 Deficiency Disorder.
Frontiers in neurology   20 juin 2022
Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development.
Nature communications   18 mai 2022