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Soins; La Revue De Reference Infirmiere|June 22, 2020
[Migrant health and ethical requirements]Antoinette Bernabe-GelotSoins; La Revue De Reference Infirmiere|February 9, 2012
[The mortuary: a place of life]Antoinette Bernabe GelotFrontiers in Neuroscience|September 25, 2020
Progression of Fetal Brain Lesions in Tuberous Sclerosis ComplexAntoinette Bernabe Gelot, Alfonso RepresaEpilepsia|February 20, 2025
Cytomegalic parvalbumin neurons in fetal cases of hemimegalencephalyAntoinette-Bernabe Gelot, Tangra Ondina Draia-Nicolau, Rémi Mathieu, et al.Human Molecular Genetics|November 15, 2011
A glial origin for periventricular nodular heterotopia caused by impaired expression of Filamin-AAurelie Carabalona, Shirley Beguin, Emilie Pallesi-Pocachard, et al.Neurology. Genetics|March 4, 2021
New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromesStéphanie Bauché, Alain Sureau, Damien Sternberg, et al.Birth Defects Research|December 2, 2017
In utero ultrasound diagnosis of corpus callosum agenesis leading to the identification of orofaciodigital type 1 syndrome in female fetusesCaroline Alby, Lucile Boutaud, Maryse Bonnière, et al.Brain : a Journal of Neurology|October 4, 2017
WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cellsMara Cavallin, Maria A Rujano, Nathalie Bednarek, et al.Nature Genetics|April 8, 2015
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunctionNaiara Akizu, Vincent Cantagrel, Maha S Zaki, et al.Pageof 1