Mireille Castanet

Mutations in the selenocysteine insertion sequence–binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans

Erik Schoenmakers, Maura Agostini, Catherine Mitchell et al. · Journal of Clinical Investigation · 2010 · 310 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Management of Graves’ Disease during Pregnancy: The Key Role of Fetal Thyroid Gland Monitoring

Dominique Luton, Isabelle Le Gac, Edith Vuillard et al. · The Journal of Clinical Endocrinology & Metabolism · 2005 · 297 citations · Full text

Medicine, Endocrinology, Obstetrics +17

Nineteen Years of National Screening for Congenital Hypothyroidism: Familial Cases with Thyroid Dysgenesis Suggest the Involvement of Genetic Factors

Mireille Castanet, Michel Polak, Catherine Bonaïti‐Pellié et al. · The Journal of Clinical Endocrinology & Metabolism · 2001 · 232 citations · Full text

Medicine, Endocrinology, Pediatrics +12

Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case

Aurore Carré, Gabor Szinnai, Mireille Castanet et al. · Human Molecular Genetics · 2009 · 211 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

European cystic fibrosis bone mineralisation guidelines

Isabelle Sermet‐Gaudelus, Maria Luisa Bianchi, Michèle Garabédian et al. · Journal of Cystic Fibrosis · 2011 · 186 citations

Medicine, Orthopaedic Surgery, Bone Metabolism +7