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Birth Defects Research. Part A, Clinical and Molecular Teratology|May 19, 2011
Tbx1, subpulmonary myocardium and conotruncal congenital heart defectsPauline Parisot, Karim Mesbah, Magali Théveniau-Ruissy, et al.Journal of Anatomy|January 16, 2013
The pattern of the coronary arterial orifices in hearts with congenital malformations of the outflow tracts: a marker of rotation of the outflow tract during cardiac development?Lucile Houyel, Fanny Bajolle, André Capderou, et al.Developmental Dynamics : an Official Publication of the American Association of Anatomists|December 29, 2015
Coronary stem development in wild-type and Tbx1 null mouse heartsMagali Théveniau-Ruissy, José-Maria Pérez-Pomares, Pauline Parisot, et al.Clinical Genetics|March 30, 2026
Homozygous Loss-of-Function Variant in SLC20A1 Coding for Ubiquitous Phosphate Transporter PiT1 Is Associated With Multiple Developmental AbnormalitiesEugénie Koumakis, Céline Huber, Wendy Chung, et al.Radiology|June 10, 2020
Cardiac MRI in Children with Multisystem Inflammatory Syndrome Associated with COVID-19Eléonore Blondiaux, Pauline Parisot, Alban Redheuil, et al.Translational Pediatrics|June 12, 2023
Comparison of telerobotic and conventional ultrasonography in children: a crossover bicentric pilot studyCeline Delestrain, Camille Jung, Aline Malterre, et al.Cardiology in the Young|May 27, 2016
Neonatal management and outcomes of prenatally diagnosed CHDsMyriam Bensemlali, Fanny Bajolle, Daniela Laux, et al.Acta Paediatrica (Oslo, Norway : 1992)|November 15, 2020
Multisystem inflammatory syndrome in children rose and fell with the first wave of the COVID-19 pandemic in FranceRicardo Carbajal, Mathie Lorrot, Yael Levy, et al.Journal of Medical Genetics|October 2, 2012
Antenatal spectrum of CHARGE syndrome in 40 fetuses with CHD7 mutationsMarine Legendre, Marie Gonzales, Géraldine Goudefroye, et al.Pageof 1