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Sophie Naudion

Showing results (1-10 of 43) with videos related to

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Annales De Pathologie|December 17, 2009
[Maze-like vascular anomaly in partial mole. Interest for the pathological diagnosis of partial mole on chorionic villous sampling]Dominique Carles, Fanny Pelluard, Gwenaëlle André, et al.
Annales De Pathologie|July 4, 2012
[Cardiac tamponade with anterior interventricular vein thrombosis complicating central venous catheter insertion in a neonate]Dominique Carles, Christian Boucard, Béatrice Baudoin, et al.
Annales De Pathologie|August 20, 2013
[Placental pathology of uteroplacental vascular deficiency]Dominique Carles, Fanny Pelluard, Gwenaëlle André, et al.
Molecular Genetics and Metabolism|August 8, 2013
Expanding the clinical phenotype at the 3q13.31 locus with a new case of microdeletion and first characterization of the reciprocal duplicationMarie-Laure Vuillaume, Marie-Ange Delrue, Sophie Naudion, et al.
Gynecologie, Obstetrique, Fertilite & Senologie|March 20, 2023
[Management of isolated increased nuchal translucency: survey among the Pluridisciplinary Centers for Prenatal Diagnosis]Manon De Vriendt, Caroline Rooryck, Frédéric Coatleven, et al.
Acta Obstetricia Et Gynecologica Scandinavica|February 18, 2025
Outcomes associated with fetal nuchal translucency between 3.0 and 3.4 mm in the first trimesterManon D E Vriendt, Caroline Rooryck, Hugo Madar, et al.
Journal of Autism and Developmental Disorders|April 8, 2009
Socio-behavioral characteristics of children with Rubinstein-Taybi syndromeCédric Galéra, Emmanuelle Taupiac, Sonia Fraisse, et al.
Mitochondrion|February 19, 2026
Phenotypic description and functional characterization of the mitochondrial disease associated with the SFXN4 geneSarah Courtois, Chloé Angelini, Juliette Preud'homme, et al.
Acta Neuropathologica Communications|April 16, 2020
Foetal onset of EIF2B related disorder in two siblings: cerebellar hypoplasia with absent Bergmann glia and severe hypomyelinationAurélien Trimouille, Florent Marguet, Fanny Sauvestre, et al.
Clinical Genetics|January 12, 2019
Fetal phenotype of Rubinstein-Taybi syndrome caused by CREBBP mutationsJulien Van-Gils, Sophie Naudion, Jérôme Toutain, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
Annales De Pathologie|December 17, 2009
[Maze-like vascular anomaly in partial mole. Interest for the pathological diagnosis of partial mole on chorionic villous sampling]Dominique Carles, Fanny Pelluard, Gwenaëlle André, et al.
Annales De Pathologie|July 4, 2012
[Cardiac tamponade with anterior interventricular vein thrombosis complicating central venous catheter insertion in a neonate]Dominique Carles, Christian Boucard, Béatrice Baudoin, et al.
Annales De Pathologie|August 20, 2013
[Placental pathology of uteroplacental vascular deficiency]Dominique Carles, Fanny Pelluard, Gwenaëlle André, et al.
Molecular Genetics and Metabolism|August 8, 2013
Expanding the clinical phenotype at the 3q13.31 locus with a new case of microdeletion and first characterization of the reciprocal duplicationMarie-Laure Vuillaume, Marie-Ange Delrue, Sophie Naudion, et al.
Gynecologie, Obstetrique, Fertilite & Senologie|March 20, 2023
[Management of isolated increased nuchal translucency: survey among the Pluridisciplinary Centers for Prenatal Diagnosis]Manon De Vriendt, Caroline Rooryck, Frédéric Coatleven, et al.
Acta Obstetricia Et Gynecologica Scandinavica|February 18, 2025
Outcomes associated with fetal nuchal translucency between 3.0 and 3.4 mm in the first trimesterManon D E Vriendt, Caroline Rooryck, Hugo Madar, et al.
Journal of Autism and Developmental Disorders|April 8, 2009
Socio-behavioral characteristics of children with Rubinstein-Taybi syndromeCédric Galéra, Emmanuelle Taupiac, Sonia Fraisse, et al.
Mitochondrion|February 19, 2026
Phenotypic description and functional characterization of the mitochondrial disease associated with the SFXN4 geneSarah Courtois, Chloé Angelini, Juliette Preud'homme, et al.
Acta Neuropathologica Communications|April 16, 2020
Foetal onset of EIF2B related disorder in two siblings: cerebellar hypoplasia with absent Bergmann glia and severe hypomyelinationAurélien Trimouille, Florent Marguet, Fanny Sauvestre, et al.
Clinical Genetics|January 12, 2019
Fetal phenotype of Rubinstein-Taybi syndrome caused by CREBBP mutationsJulien Van-Gils, Sophie Naudion, Jérôme Toutain, et al.
Pageof 5