Muriel Houang

Paris, France

Last Updated: 09/26/2026

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Found 24 publications

RAS/MAPK pathway modulation with simvastatin in children with Noonan syndrome: a multicentre, randomised, double-blind, placebo-controlled phase 3 trial.

RAS/MAPK pathway modulation with simvastatin in children with Noonan syndrome: a multicentre, randomised, double-blind, placebo-controlled phase 3 trial.

Journal: EClinicalMedicine

Published: March 24, 2026

Rationalizing thrombophilia screening in children: Insights from a 2019 retrospective study at a tertiary care hospital.

Rationalizing thrombophilia screening in children: Insights from a 2019 retrospective study at a tertiary care hospital.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: September 08, 2025

Splenic structural and functional abnormalities in individuals with NR5A1/SF-1 variants.

Splenic structural and functional abnormalities in individuals with NR5A1/SF-1 variants.

Journal: Endocrine connections

Published: August 23, 2025

A Recurrent Splice Variant Sheds Light on 11β-Hydroxylase Deficiency in a Unique Large Cohort.

A Recurrent Splice Variant Sheds Light on 11β-Hydroxylase Deficiency in a Unique Large Cohort.

Journal: The Journal of clinical endocrinology and metabolism

Published: May 28, 2025

Advances in congenital adrenal hyperplasia newborn screening: 11-ketotestosterone and 21-deoxycortisone as additional discriminatory biomarkers.

Advances in congenital adrenal hyperplasia newborn screening: 11-ketotestosterone and 21-deoxycortisone as additional discriminatory biomarkers.

Journal: European journal of endocrinology

Published: May 23, 2025

Digenic Inheritance Mode in Congenital Hypothyroidism Due to Thyroid Dysgenesis: HYPOTYGEN Translational Cohort Study.

Digenic Inheritance Mode in Congenital Hypothyroidism Due to Thyroid Dysgenesis: HYPOTYGEN Translational Cohort Study.

Journal: The Journal of clinical endocrinology and metabolism

Published: October 19, 2024

Contribution of Clinical and Biological Mini-Puberty and Genetic Analysis in 57 46,XY Differences of Sex Development: A Monocentric Retrospective Cohort.

Contribution of Clinical and Biological Mini-Puberty and Genetic Analysis in 57 46,XY Differences of Sex Development: A Monocentric Retrospective Cohort.

Journal: Hormone research in paediatrics

Published: March 12, 2024

Plasma 21-deoxycortisone: a sensitive additive tool in 21-hydroxylase deficiency in newborns.

Plasma 21-deoxycortisone: a sensitive additive tool in 21-hydroxylase deficiency in newborns.

Journal: European journal of endocrinology

Published: October 23, 2023

Changes in the clinical management of 5α-reductase type 2 and 17β-hydroxysteroid dehydrogenase type 3 deficiencies in France.

Changes in the clinical management of 5α-reductase type 2 and 17β-hydroxysteroid dehydrogenase type 3 deficiencies in France.

Journal: Endocrine connections

Published: October 18, 2022

Combining metabolomics and machine learning models as a tool to distinguish non-classic 21-hydroxylase deficiency from polycystic ovary syndrome without adrenocorticotropic hormone testing.

Combining metabolomics and machine learning models as a tool to distinguish non-classic 21-hydroxylase deficiency from polycystic ovary syndrome without adrenocorticotropic hormone testing.

Journal: Human reproduction (Oxford, England)

Published: June 18, 2022

Analysis of a pitfall in congenital adrenal hyperplasia newborn screening: evidence of maternal use of corticoids detected on dried blood spot.

Analysis of a pitfall in congenital adrenal hyperplasia newborn screening: evidence of maternal use of corticoids detected on dried blood spot.

Journal: Endocrine connections

Published: April 06, 2022

Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol).

Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol).

Journal: Orphanet journal of rare diseases

Published: February 28, 2022

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Last Updated: 09/26/2026