Publications by authors named "M Houang"

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Splenic structural and functional abnormalities in individuals with NR5A1/SF-1 variants.
Khadidja Fouatih, Camille Roussel, Maryse Cartigny, Muriel Houang, Lise Duranteau

Endocr Connect· December 2025

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Advances in congenital adrenal hyperplasia newborn screening: 11-ketotestosterone and 21-deoxycortisone as additional discriminatory biomarkers.
Coumba Sow, Thao Nguyen-Khoa, Caroline Moreau, Jean Fiet, Guillaume Bachelot, Muriel Houang

Eur J Endocrinol· November 2025

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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, Muriel Houang

J Clin Endocrinol Metab· September 2025

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A recurrent splice variant sheds light on 11beta-hydroxylase deficiency in a unique large cohort.
Clément Janot, Delphine Mallet, Alexandre Janin, Jérome Bertherat, Raja Brauner, Muriel Houang

J Clin Endocrinol Metab· August 2025

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Contribution of Clinical and Biological Mini-Puberty and Genetic Analysis in 57 46,XY Differences of Sex Development: A Monocentric Retrospective Cohort.
Chloé Marie, Lucie Tosca, Jérôme Bouligand, Abd-El-Kader Ait-Tayeb, Severine Trabado, Muriel Houang

Horm Res Paediatr· January 2025

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