Publications by authors named "Catherine Raynaud-Ravni"

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Digenic Inheritance Mode in Congenital Hypothyroidism Due to Thyroid Dysgenesis: HYPOTYGEN Translational Cohort Study.
Athanasia Stoupa, Dulanjalee Kariyawasam, Fabienne Jabot-Hanin, Adrien Nguyen-Quoc, Sylvain Hanein, Catherine Raynaud-Ravni

J Clin Endocrinol Metab· September 2025

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Thyroid Hypoplasia in Congenital Hypothyroidism Associated with Thyroid Peroxidase Mutations.
Athanasia Stoupa, Rim Chaabane, Manelle Guériouz, Catherine Raynaud-Ravni, Patrick Nitschke

Thyroid· July 2018

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Sporadic and genetic forms of paediatric somatotropinoma: a retrospective analysis of seven cases and a review of the literature.
Cécile Nozières, Pascale Berlier, Clémentine Dupuis, Catherine Raynaud-Ravni, Yves Morel

Orphanet J Rare Dis· October 2011

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Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case.
Aurore Carré, Gabor Szinnai, Mireille Castanet, Sylvia Sura-Trueba, Elodie Tron, Catherine Raynaud-Ravni

Hum Mol Genet· June 2009

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