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Jean-Michel PEDESPAN | Centre Hospitalier Universitaire de Bordeaux,  Bordeaux | CHU Bordeaux | Research profile
Jean-Michel PEDESPAN | Centre Hospitalier Universitaire de Bordeaux, Bordeaux | CHU Bordeaux | Research profile

Hydrocéphalie, spina bifida: des enfants en bas-âge opérés - Ô cameroun !
Hydrocéphalie, spina bifida: des enfants en bas-âge opérés - Ô cameroun !

Human Mutation: Vol 41, No 3
Human Mutation: Vol 41, No 3

Jean-Michel PEDESPAN | Centre Hospitalier Universitaire de Bordeaux,  Bordeaux | CHU Bordeaux | Research profile
Jean-Michel PEDESPAN | Centre Hospitalier Universitaire de Bordeaux, Bordeaux | CHU Bordeaux | Research profile

jean-michel PEDESPAN - MEDECIN PEDIATRE - Bordeaux Hospital University  Center (CHU) | LinkedIn
jean-michel PEDESPAN - MEDECIN PEDIATRE - Bordeaux Hospital University Center (CHU) | LinkedIn

Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of  cortical development and microcephaly. - Abstract - Europe PMC
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. - Abstract - Europe PMC

Frontiers | Results From an Italian Expanded Access Program on Cannabidiol  Treatment in Highly Refractory Dravet Syndrome and Lennox–Gastaut Syndrome
Frontiers | Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox–Gastaut Syndrome

L'A.P.R.A.T.
L'A.P.R.A.T.

Docteur Pedespan Jean-Michel Bordeaux Pédiatre 33000, téléphone et avis
Docteur Pedespan Jean-Michel Bordeaux Pédiatre 33000, téléphone et avis

Programme NOP Bordeaux 2018 - Pr Brémond-Gignac V5
Programme NOP Bordeaux 2018 - Pr Brémond-Gignac V5

Maternité d'Oloron : les médecins alertent
Maternité d'Oloron : les médecins alertent

DNA repair functional analyses of NBN hypomorphic variants associated with  NBN‐related infertility | Institut Curie
DNA repair functional analyses of NBN hypomorphic variants associated with NBN‐related infertility | Institut Curie

Delineating FOXG1 syndrome | Neurology Genetics
Delineating FOXG1 syndrome | Neurology Genetics

Frédéric Joliot Institute for Life Sciences - NeuroSpin
Frédéric Joliot Institute for Life Sciences - NeuroSpin

Childhood demyelinating diseases with a prolonged remitting course and  their relation to Schilder's disease: report of two cases | Journal of  Neurology, Neurosurgery & Psychiatry
Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder's disease: report of two cases | Journal of Neurology, Neurosurgery & Psychiatry

☎️ Contacts du Dr Jean Michel Pedespan, Pediatre à Bordeaux 33000
☎️ Contacts du Dr Jean Michel Pedespan, Pediatre à Bordeaux 33000

Infantile Alexander Disease: Spectrum of GFAP Mutations and  Genotype-Phenotype Correlation - ScienceDirect
Infantile Alexander Disease: Spectrum of GFAP Mutations and Genotype-Phenotype Correlation - ScienceDirect

Pédiatre Jean-Michel Pedespan Agenda en ligne Pédiatre
Pédiatre Jean-Michel Pedespan Agenda en ligne Pédiatre

Jean-Michel PEDESPAN | Centre Hospitalier Universitaire de Bordeaux,  Bordeaux | CHU Bordeaux | Research profile
Jean-Michel PEDESPAN | Centre Hospitalier Universitaire de Bordeaux, Bordeaux | CHU Bordeaux | Research profile

jean-michel PEDESPAN - MEDECIN PEDIATRE - Bordeaux Hospital University  Center (CHU) | LinkedIn
jean-michel PEDESPAN - MEDECIN PEDIATRE - Bordeaux Hospital University Center (CHU) | LinkedIn

Pédespan, Jean-Michel | Canal U
Pédespan, Jean-Michel | Canal U

Table of Contents page: Brain and Development
Table of Contents page: Brain and Development

Benign nocturnal alternating hemiplegia of childhood: Two cases with  positive evolution - ScienceDirect
Benign nocturnal alternating hemiplegia of childhood: Two cases with positive evolution - ScienceDirect