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1787 results found for your search

  • activite recherche

    Research Acceleration

    CRISPR/Cas9: a patch on the DNA double helix?

  • Cellules

    Research Acceleration

    How the study of genetic diseases contributes to knowledge in cancerology

  • Equipe Edor Kabashi et Rima Nabout

    Research Acceleration

    Diagnosing a common genetic mutation in multiple patients using unstructured health data

  • Adult neurogenesis: beyond learning and memory.

    Johanne Dubail

    Source :

    Annu Rev Psychol

    2015 Jan 3

    Pmid / DOI:

    25251485

  • Complete hemispherotomy leads to lateralized functional organization and lower level of consciousness in the isolated hemisphere.

    Thomas Blauwblomme, Ludovic Fillon, Nathalie Boddaert, Rima NABBOUT, Jean-Marc Tacchella, Volodia Dangouloff-Ros

    Source :

    Epilepsia Open

    2020 Dec 1

    Pmid / DOI:

    33336125

  • En-tête pages équipes

    Research Acceleration

    Type 1 interferopathies: keys to understanding clinical and tissue variations

  • Cellules du colon

    Research Acceleration

      Portrait

    Marianna Parlato, a young researcher dedicated to inflammatory bowel diseases

  • MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate and is mutated in Pontocerebellar Hypoplasia.

    Ekin ucuncu, Karthyayani Rajamani , Nami Altin, Pierre David, Giulia Barcia, Nathalie Lefort, Céline BANAL, Patrick Nitschké, Arnold Munnich, Nadia Bahi-Buisson, Lydie Burglen, Nathalie Boddaert, Vincent Cantagrel

    Source :

    Nat Commun

    2020 Nov 30

    Pmid / DOI:

    33257696

  • Staff

    Research Acceleration

    Integrated care and research programs

  • MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia.

    Lydie Burglen

    Source :

    Ann Neurol

    2021 Jan 14

    Pmid / DOI:

    33443317

  • Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development.

    Lydie Burglen

    Source :

    Neuron

    2020 May 6

    Pmid / DOI:

    32135084

  • Equipe Edor Kabashi et Rima Nabout

    Research Acceleration

    Rare epilepsies, where do we stand?