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authFullName_s : Marie Brasseur-Daudruy

Pyridoxine-dependent epilepsy: report on three families with neuropathology

Florent Marguet , Hager Barakizou , Abdellah Tebani , Lénaïg Abily-Donval , Stéphanie Torre , et al.
Metabolic Brain Disease, 2016, 31 (6), pp.1435-1443. ⟨10.1007/s11011-016-9869-z⟩
Journal articles hal-02453949v1

[Postnatal imaging of prenatally diagnosed malformation of the urinary tract]

Jean-Nicolas Dacher , Pierre-Hugues Vivier , Michael Dolores , Marie Brasseur-Daudruy , Danielle Eurin
Archives de Pédiatrie, 2008, 15 (5), pp.884-6. ⟨10.1016/S0929-693X(08)71952-3⟩
Journal articles istex inserm-00472922v1
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Clinical and molecular description of 19 patients with GATAD2B-Associated Neurodevelopmental Disorder (GAND)

Gabriella Vera , Arthur Sorlin , Geoffroy Delplancq , François Lecoquierre , Marie Brasseur-Daudruy , et al.
European Journal of Medical Genetics, 2020, pp.104004. ⟨10.1016/j.ejmg.2020.104004⟩
Journal articles hal-02904491v1

Post hemorrhagic hydrocephalus and neurodevelopmental outcomes in a context of neonatal intraventricular hemorrhage: an institutional experience in 122 preterm children

Vianney Gilard , Alexandra Chadie , François-Xavier Ferracci , Marie Brasseur-Daudruy , François Proust , et al.
BMC Pediatrics, 2018, 18 (1), ⟨10.1186/s12887-018-1249-x⟩
Journal articles hal-02451609v1

Whole-body MR imaging in suspected physical child abuse: comparison with skeletal survey and bone scintigraphy findings from the PEDIMA prospective multicentre study

Maïa Proisy , Pierre-Hugues Vivier , Baptiste Morel , Bertrand Bruneau , Catherine Sembely-Taveau , et al.
European Radiology, 2021, Online ahead of print. ⟨10.1007/s00330-021-07896-9⟩
Journal articles inserm-03214574v1

Severe apparently isolated fetal ventriculomegaly and neurodevelopmental outcome

Mathilde Letouzey , Alexandra Chadie , Marie Brasseur-Daudruy , François Proust , Eric Verspyck , et al.
Prenatal Diagnosis, 2017, 37 (8), pp.820-826. ⟨10.1002/pd.5095⟩
Journal articles hal-02452301v1

Confirmation and further delineation of the SMG9‐deficiency syndrome, a rare and severe developmental disorder

François Lecoquierre , Antoine Bonnevalle , Alexandra Chadie , Claire Gayet , Clémentine Dumant-Forest , et al.
American Journal of Medical Genetics Part A, 2019, 179 (11), pp.2257-2262. ⟨10.1002/ajmg.a.61317⟩
Journal articles hal-02356422v1

Neurodevelopmental outcome in prenatally diagnosed isolated agenesis of the corpus callosum

Lise Folliot-Le Doussal , Alexandra Chadie , Marie Brasseur-Daudruy , Eric Verspyck , Pascale Saugier-Veber , et al.
Early Human Development, 2018, 116, pp.9-16. ⟨10.1016/j.earlhumdev.2017.10.004⟩
Journal articles hal-02451670v1