Pauline Parisot
Paris, France
Last Updated: 09/26/2026
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Found 10 publications
Homozygous Loss-of-Function Variant in SLC20A1 Coding for Ubiquitous Phosphate Transporter PiT1 Is Associated With Multiple Developmental Abnormalities.
Journal: Clinical genetics
Published: January 06, 2026
Comparison of telerobotic and conventional ultrasonography in children: a crossover bicentric pilot study.
Journal: Translational pediatrics
Published: November 04, 2022
Multisystem inflammatory syndrome in children rose and fell with the first wave of the COVID-19 pandemic in France.
Journal: Acta paediatrica (Oslo, Norway : 1992)
Published: August 28, 2020
Cardiac MRI in Children with Multisystem Inflammatory Syndrome Associated with COVID-19.
Journal: Radiology
Published: June 10, 2020
Neonatal management and outcomes of prenatally diagnosed CHDs.
Journal: Cardiology in the young
Published: May 27, 2016
Coronary stem development in wild-type and Tbx1 null mouse hearts.
Journal: Developmental dynamics : an official publication of the American Association of Anatomists
Published: September 25, 2015
Malformations, genetic abnormalities, and Wilms tumor.
Journal: Pediatric blood & cancer
Published: April 23, 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?
Journal: Journal of anatomy
Published: December 05, 2012
Neonatal collapse: diagnosis of myocarditis
Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Published: November 05, 2012
Antenatal spectrum of CHARGE syndrome in 40 fetuses with CHD7 mutations.
Journal: Journal of medical genetics
Published: October 02, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026