Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. - Abstract - Europe PMC
Tactile Temporal Discrimination Is Impaired in Myoclonus‐Dystonia - Tarrano - 2020 - Movement Disorders - Wiley Online Library
Frédéric Joliot Institute for Life Sciences - NeuroSpin
Journal of Neurosurgery Volume 83 Issue 6 () Journals
Pédespan, Jean-Michel | Canal U
jean-michel PEDESPAN - MEDECIN PEDIATRE - Bordeaux Hospital University Center (CHU) | LinkedIn
Delineating FOXG1 syndrome | Neurology Genetics
☎️ Contacts du Dr Jean Michel Pedespan, Pediatre à Bordeaux 33000
De novo ATP1A3 variants cause polymicrogyria | Science Advances
Jean-Michel PEDESPAN | Centre Hospitalier Universitaire de Bordeaux, Bordeaux | CHU Bordeaux | Research profile
Frontiers | Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox–Gastaut Syndrome
Benign nocturnal alternating hemiplegia of childhood: Two cases with positive evolution - ScienceDirect
Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy | European Journal of Human Genetics
Hydrocéphalie, spina bifida: des enfants en bas-âge opérés - Ô cameroun !
Statistical Analysis of Mitochondrial Pathologies in Childhood: Identification of Deficiencies Using Principal Component Analysis | Laboratory Investigation
L'A.P.R.A.T.
Jean-Michel PEDESPAN | Centre Hospitalier Universitaire de Bordeaux, Bordeaux | CHU Bordeaux | Research profile
Pourquoi protéger nos petits des écrans ? - Léa&Léo
To work, in all independence, in favour of quality healthcare, first and foremost in the interest of patients (...).” (Art
Maternité d'Oloron : les médecins alertent
Jean-Michel PEDESPAN | Centre Hospitalier Universitaire de Bordeaux, Bordeaux | CHU Bordeaux | Research profile
Human Mutation: Vol 41, No 3
