Publications by authors named "Mireille Castanet"

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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, Mireille Castanet

J Clin Endocrinol Metab· September 2025

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Correction: Partially hydrolyzed, whey-based infant formula with six human milk oligosaccharides, LMG11588, and CNCM I-3446 is safe, well tolerated, and improves gut health: a staged analysis of a randomized trial.
Jean-Charles Picaud, Olivier Claris, Mercedes Gil-Campos, Ignacio Salamanca De La Cueva, Luc Cornette, Mireille Castanet

Front Nutr· September 2025

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Partially hydrolyzed, whey-based infant formula with six human milk oligosaccharides, LMG11588, and CNCM I-3446 is safe, well tolerated, and improves gut health: a staged analysis of a randomized trial.
Jean-Charles Picaud, Olivier Claris, Mercedes Gil-Campos, Ignacio Salamanca De La Cueva, Luc Cornette, Mireille Castanet

Front Nutr· July 2025

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Differential alternative splicing analysis links variation in ZRSR2 to a novel type of oral-facial-digital syndrome.
Laurens Hannes, Marta Atzori, Alice Goldenberg, Jesús Argente, Tania Attie-Bitach, Mireille Castanet

Genet Med· April 2024

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Off-label use of cinacalcet in pediatric primary hyperparathyroidism: A French multicenter experience.
Julie Bernardor, Sacha Flammier, Jean-Pierre Salles, Cyril Amouroux, Mireille Castanet

Front Pediatr· August 2022

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The invention of aldosterone, how the past resurfaces in pediatric endocrinology.
Say Viengchareun, Eric Pussard, Mireille Castanet, Laurent M Sachs, Thi An Vu

Mol Cell Endocrinol· September 2021

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Steroidogenic cell microenvironment and adrenal function in physiological and pathophysiological conditions.
Antoine-Guy Lopez, Céline Duparc, Julien Wils, Alexandre Naccache, Mireille Castanet

Mol Cell Endocrinol· September 2021

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Role of Mast Cells in the Control of Aldosterone Secretion.
Antoine-Guy Lopez, Céline Duparc, Alexandre Naccache, Mireille Castanet, Hervé Lefebvre

Horm Metab Res· June 2020

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Early Effect of Supplemented Infant Formulae on Intestinal Biomarkers and Microbiota: A Randomized Clinical Trial.
Mireille Castanet, Christos Costalos, Nadja Haiden, Jean-Michel Hascoet, Bernard Berger

Nutrients· 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, Mireille Castanet

Eur J Med Genet· November 2019

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Paracrine Regulation of Aldosterone Secretion in Physiological and Pathophysiological Conditions.
Hervé Lefebvre, Céline Duparc, Alexandre Naccache, Antoine-Guy Lopez, Mireille Castanet

Vitam Horm· April 2019

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Hyperinsulinemic Hypoglycemia in a Neonate.
Anais Melin, Charles Brossard, Mireille Castanet, Soumeya Bekri, Abdellah Tebani

Clin Chem· February 2019

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Fertility Preservation in Klinefelter Syndrome Patients during the Transition Period.
Nathalie Rives, Aurélie Rives, Christine Rondanino, Mireille Castanet, Ariane Cuny

Endocr Dev· July 2018

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mutations are responsible for autosomal recessive osteogenesis imperfecta.
Mathilde Doyard, Séverine Bacrot, Céline Huber, Maja Di Rocco, Alice Goldenberg, Mireille Castanet

J Med Genet· April 2018

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Temporal and spatial distribution of mast cells and steroidogenic enzymes in the human fetal adrenal.
Alexandre Naccache, Estelle Louiset, Céline Duparc, Annie Laquerrière, Sophie Patrier, Mireille Castanet

Mol Cell Endocrinol· October 2016

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Metallic Profile of Whole Blood and Plasma in a Series of 99 Healthy Children.
Jean-Pierre Goullé, Pascal Le Roux, Mireille Castanet, Loïc Mahieu, Stéphanie Guyet-Job

J Anal Toxicol· August 2016

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Molecular insights into the possible role of Kir4.1 and Kir5.1 in thyroid hormone biosynthesis.
Helton Estrela Ramos, Magnus Régios Dias da Silva, Aurore Carré, Joaquim Custódio Silva, Rolf Matias Paninka, Mireille Castanet

Horm Res Paediatr· December 2015

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Natural history and management of congenital hypothyroidism with in situ thyroid gland.
Mireille Castanet, Alexandra Goischke, Juliane Léger, Caroline Thalassinos, Daniele Rodrigue

Horm Res Paediatr· December 2015

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Functional characterization of the novel sequence variant p.S304R in the hinge region of TSHR in a congenital hypothyroidism patients and analogy with other formerly known mutations of this gene portion.
Taise Lima Oliveira Cerqueira, Aurore Carré, Lucie Chevrier, Gabor Szinnai, Elodie Tron, Mireille Castanet

J Pediatr Endocrinol Metab· July 2015

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Pharmacokinetic study of metopimazine by oral route in children.
Eric Mallet, Frederic Bounoure, Mohamed Skiba, Elodie Saussereau, Jean-Pierre Goullé, Mireille Castanet

Pharmacol Res Perspect· June 2015

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A novel FOXE1 mutation (R73S) in Bamforth-Lazarus syndrome causing increased thyroidal gene expression.
Aurore Carré, Rasha T Hamza, Dulanjalee Kariyawasam, Loïc Guillot, Raphaël Teissier, Mireille Castanet

Thyroid· April 2014

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Lightwood syndrome revisited with a novel mutation in CYP24 and vitamin D supplement recommendations.
Mireille Castanet, Eric Mallet, Marie-Laure Kottler

J Pediatr· October 2013

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Multiplex Ligation-dependent Probe Amplification improves the detection rate of NKX2.1 mutations in patients affected by brain-lung-thyroid syndrome.
Raphaël Teissier, Loïc Guillot, Aurore Carré, Melina Morandini, Chantal Stuckens, Mireille Castanet

Horm Res Paediatr· August 2012

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European cystic fibrosis bone mineralisation guidelines.
Isabelle Sermet-Gaudelus, Maria Luisa Bianchi, Michèle Garabédian, Robert M Aris, Alison Morton, Mireille Castanet

J Cyst Fibros· June 2011

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Hes1 is required for appropriate morphogenesis and differentiation during mouse thyroid gland development.
Aurore Carre, Latif Rachdi, Elodie Tron, Bénédicte Richard, Mireille Castanet

PLoS One· February 2011

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