Nadia Coudray

<i>CYP24A1</i>Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait

Arnaud Molin, R. Baudoin, Martin Kaufmann et al. · The Journal of Clinical Endocrinology & Metabolism · 2015 · 141 citations · Full text

Medicine, Endocrinology, Genetics +17

A New Deletion Ablating NESP55 Causes Loss of Maternal Imprint of A/B<i>GNAS</i>and Autosomal Dominant Pseudohypoparathyroidism Type Ib

Nicolas Richard, Geneviève Abéguilé, Nadia Coudray et al. · The Journal of Clinical Endocrinology & Metabolism · 2012 · 97 citations

Medicine, Endocrinology, Genetics +17

Paternal<i>GNAS</i>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 et al. · The Journal of Clinical Endocrinology & Metabolism · 2013 · 79 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Vitamin D–Dependent Rickets Type 1B (25-Hydroxylase Deficiency): A Rare Condition or a Misdiagnosed Condition?

Arnaud Molin, Arnaud Wiedemann, Nick Demers et al. · Journal of Bone and Mineral Research · 2017 · 76 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Left ventricular diastolic function in asymptomatic and symptomatic human immunodeficiency virus carriers: an echocardiographic study

Nadia Coudray, D. De Zuttère, Gilles Force et al. · European Heart Journal · 1995 · 55 citations

Medicine, Cardiology, Internal Medicine +14