Publications by authors named "Nadia Coudray"

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Overlapping Phenotypes Associated With , , and Mutations: A Cohort Study of Patients With Hypersensitivity to Vitamin D.
Arnaud Molin, Sandrine Lemoine, Martin Kaufmann, Pierre Breton, Marie Nowoczyn, Nadia Coudray

Front Endocrinol (Lausanne)· February 2022

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Maternal Transmission Ratio Distortion of GNAS Loss-of-Function Mutations.
Sarah Snanoudj, Arnaud Molin, Cindy Colson, Nadia Coudray, Sylvie Paulien

J Bone Miner Res· May 2020

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Molecular characterization of a recurrent 10.9 kb CYP24A1 deletion in Idiopathic Infantile Hypercalcemia.
Arnaud Molin, Marie Nowoczyn, Nadia Coudray, Céline Ballandone, Geneviève Abéguilé

Eur J Med Genet· November 2019

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High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B.
Cindy Colson, Matthieu Decamp, Nicolas Gruchy, Nadia Coudray, Céline Ballandonne

Bone· June 2019

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Vitamin D-Dependent Rickets Type 1B (25-Hydroxylase Deficiency): A Rare Condition or a Misdiagnosed Condition?
Arnaud Molin, Arnaud Wiedemann, Nick Demers, Martin Kaufmann, Jérémy Do Cao, Nadia Coudray

J Bone Miner Res· September 2017

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Paternal GNAS mutations lead to severe intrauterine growth retardation (IUGR) and provide evidence for a role of XLαs in fetal development.
Nicolas Richard, Arnaud Molin, Nadia Coudray, Pauline Rault-Guillaume, Harald Jüppner

J Clin Endocrinol Metab· September 2013

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A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib.
Nicolas Richard, Genevieve Abeguilé, Nadia Coudray, Hervé Mittre, Nicolas Gruchy

J Clin Endocrinol Metab· May 2012

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