Delphine Zenaty

150, Rue De Charenton
Paris, 72012, France

Last Updated: 09/26/2026

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Found 27 publications

Real-world clinical experience with weekly somatrogon in pediatric growth hormone deficiency: A French longitudinal study with some unexpected clinical observations.

Real-world clinical experience with weekly somatrogon in pediatric growth hormone deficiency: A French longitudinal study with some unexpected clinical observations.

Journal: Annales d'endocrinologie

Published: February 19, 2026

MKRN3 Variants in Central Precocious Puberty as an Example of the Complexity to Classify Missense Variants in Imprinted Genes as Pathogenic.

MKRN3 Variants in Central Precocious Puberty as an Example of the Complexity to Classify Missense Variants in Imprinted Genes as Pathogenic.

Journal: Hormone research in paediatrics

Published: August 05, 2025

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

Position statement on the diagnosis and management of premature/primary ovarian insufficiency (except Turner Syndrome).

Position statement on the diagnosis and management of premature/primary ovarian insufficiency (except Turner Syndrome).

Journal: Annales d'endocrinologie

Published: September 11, 2021

Screening of a Large Cohort of Asymptomatic SDHx Mutation Carriers in Routine Practice.

Screening of a Large Cohort of Asymptomatic SDHx Mutation Carriers in Routine Practice.

Journal: The Journal of clinical endocrinology and metabolism

Published: September 25, 2020

Factors Affecting Loss to Follow-Up in Children and Adolescents with Chronic Endocrine Conditions.

Factors Affecting Loss to Follow-Up in Children and Adolescents with Chronic Endocrine Conditions.

Journal: Hormone research in paediatrics

Published: October 09, 2019

Positive Impact of Genetic Test on the Management and Outcome of Patients With Paraganglioma and/or Pheochromocytoma.

Positive Impact of Genetic Test on the Management and Outcome of Patients With Paraganglioma and/or Pheochromocytoma.

Journal: The Journal of clinical endocrinology and metabolism

Published: November 07, 2018

X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood.

X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood.

Journal: European journal of endocrinology

Published: October 31, 2018

High prevalence of syndromic disorders in patients with non-isolated central precocious puberty.

High prevalence of syndromic disorders in patients with non-isolated central precocious puberty.

Journal: European journal of endocrinology

Published: July 19, 2018

Early Determinants of Thyroid Function Outcomes in Children with Congenital Hypothyroidism and a Normally Located Thyroid Gland: A Regional Cohort Study.

Early Determinants of Thyroid Function Outcomes in Children with Congenital Hypothyroidism and a Normally Located Thyroid Gland: A Regional Cohort Study.

Journal: Thyroid : official journal of the American Thyroid Association

Published: July 04, 2018

Should 45,X/46,XY boys with no or mild anomaly of external genitalia be investigated and followed up?

Should 45,X/46,XY boys with no or mild anomaly of external genitalia be investigated and followed up?

Journal: European journal of endocrinology

Published: April 12, 2018

SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbook.

SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbook.

Journal: Annales d'endocrinologie

Published: January 18, 2018

Showing 1-12 of 27

Last Updated: 09/26/2026