Maryse Cartigny

Lille, France

Last Updated: 09/26/2026

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Found 14 publications

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

Lessons From Prospective Longitudinal Follow-up of a French APECED Cohort.

Lessons From Prospective Longitudinal Follow-up of a French APECED Cohort.

Journal: The Journal of clinical endocrinology and metabolism

Published: September 18, 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

Therapeutic indications and metabolic effects of metreleptin in patients with lipodystrophy syndromes: Real-life experience from a national reference network.

Therapeutic indications and metabolic effects of metreleptin in patients with lipodystrophy syndromes: Real-life experience from a national reference network.

Journal: Diabetes, obesity & metabolism

Published: February 15, 2022

Defining Reference Ranges for Serum Anti-Müllerian Hormone on a Large Cohort of Normozoospermic Adult Men Highlights New Potential Physiological Functions of AMH on FSH Secretion and Sperm Motility.

Defining Reference Ranges for Serum Anti-Müllerian Hormone on a Large Cohort of Normozoospermic Adult Men Highlights New Potential Physiological Functions of AMH on FSH Secretion and Sperm Motility.

Journal: The Journal of clinical endocrinology and metabolism

Published: January 17, 2022

Correction to: Plea for a standardized imaging approach to disorders of sex development in neonates: Consensus proposal from European Society of Paediatric Radiology task force.

Correction to: Plea for a standardized imaging approach to disorders of sex development in neonates: Consensus proposal from European Society of Paediatric Radiology task force.

Journal: Pediatric radiology

Published: June 23, 2019

In cases of familial primary ovarian insufficiency and disorders of gonadal development, consider NR5A1/SF-1 sequence variants.

In cases of familial primary ovarian insufficiency and disorders of gonadal development, consider NR5A1/SF-1 sequence variants.

Journal: Reproductive biomedicine online

Published: April 11, 2019

Plea for a standardized imaging approach to disorders of sex development in neonates: consensus proposal from European Society of Paediatric Radiology task force.

Plea for a standardized imaging approach to disorders of sex development in neonates: consensus proposal from European Society of Paediatric Radiology task force.

Journal: Pediatric radiology

Published: February 19, 2019

Mental health status of individuals with sexual development disorders: A review.

Mental health status of individuals with sexual development disorders: A review.

Journal: Journal of pediatric urology

Published: September 27, 2018

Cerebellar hypoplasia with endosteal sclerosis is a POLR3-related disorder.

Cerebellar hypoplasia with endosteal sclerosis is a POLR3-related disorder.

Journal: European journal of human genetics : EJHG

Published: September 18, 2016

SF1 and spleen development: new heterozygous mutation, literature review and consequences for NR5A1-mutated patient's management.

SF1 and spleen development: new heterozygous mutation, literature review and consequences for NR5A1-mutated patient's management.

Journal: Clinical genetics

Published: August 31, 2016

Deferring surgical treatment of ambiguous genitalia into adolescence in girls with 21-hydroxylase deficiency: a feasibility study.

Deferring surgical treatment of ambiguous genitalia into adolescence in girls with 21-hydroxylase deficiency: a feasibility study.

Journal: International journal of pediatric endocrinology

Published: July 23, 2016

Showing 1-12 of 14

Last Updated: 09/26/2026