Publications by authors named "M Proisy"

Claim this Profile
E
Extending the clinical spectrum of X-linked Tonne-Kalscheuer syndrome (TOKAS): new insights from the fetal perspective.
Silvestre Cuinat, Chloé Quélin, Claire Effray, Christèle Dubourg, Gwenaelle Le Bouar, Maia Proisy

J Med Genet· August 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
PHGDH-related microcephalic dwarfism in two fetuses: Expanding the phenotypical spectrum of L-serine biosynthesis defect.
Silvestre Cuinat, Chloé Quélin, Laurent Pasquier, Philippe Loget, Dominique Aussel, Maia Proisy

Eur J Med Genet· November 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorder.
Nuno Maia, Sven Potelle, Hamide Yildirim, Sandrine Duvet, Shyam K Akula, Maïa Proisy

Am J Hum Genet· February 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
PHACES Syndrome and Associated Anomalies: Risk Associated With Small and Large Facial Hemangiomas.
Maia Proisy, Julie Powell, Catherine McCuaig, Ramy El Jalbout, Chantale Lapierre

AJR Am J Roentgenol· August 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Multiparametric Analysis of Cerebral Development in Preterm Infants Using Magnetic Resonance Imaging.
Marine Dubois, Antoine Legouhy, Isabelle Corouge, Olivier Commowick, Baptiste Morel, Maïa Proisy

Front Neurosci· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis