Rachel Reynaud

Angers, 49000, France

Last Updated: 09/26/2026

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Found 100 publications

Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: A retrospective study of a French cohort.

Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: A retrospective study of a French cohort.

Journal: Annales d'endocrinologie

Published: May 08, 2026

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

Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: a retrospective study of a French cohort.

Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: a retrospective study of a French cohort.

Journal: Annales d'endocrinologie

Published: March 21, 2026

Unraveling the Genetic Heterogeneity of Isolated Growth Hormone Deficiency: Insights from the GENHYPOPIT Cohort.

Unraveling the Genetic Heterogeneity of Isolated Growth Hormone Deficiency: Insights from the GENHYPOPIT Cohort.

Journal: Hormone research in paediatrics

Published: February 09, 2026

Pituitary developmental gene defects and their contribution to growth hormone deficiency.

Pituitary developmental gene defects and their contribution to growth hormone deficiency.

Journal: Annales d'endocrinologie

Published: February 05, 2026

Maturity Onset Diabetes of the Young (MODY): French National Diagnosis and Care Protocol (PNDS, Protocole National de Diagnostic et de Soins).

Maturity Onset Diabetes of the Young (MODY): French National Diagnosis and Care Protocol (PNDS, Protocole National de Diagnostic et de Soins).

Journal: Orphanet journal of rare diseases

Published: October 29, 2025

Oxytocin in infants with Prader-Willi syndrome to improve dysphagia and disease trajectory.

Oxytocin in infants with Prader-Willi syndrome to improve dysphagia and disease trajectory.

Journal: Orphanet journal of rare diseases

Published: September 19, 2025

Growth hormone treatment outcomes in children with genetic isolated growth hormone deficiency.

Growth hormone treatment outcomes in children with genetic isolated growth hormone deficiency.

Journal: European journal of pediatrics

Published: September 10, 2025

Long-acting growth hormone for treating growth hormone deficiency in children: a meta-analysis of randomized controlled trials focusing on changes in body mass index.

Long-acting growth hormone for treating growth hormone deficiency in children: a meta-analysis of randomized controlled trials focusing on changes in body mass index.

Journal: The Journal of clinical endocrinology and metabolism

Published: August 25, 2025

Prevalence rates of overweight and obesity among children aged 3-5 years in the Bouches-du-Rhône department during the 2022-2023 school year: A cross-sectional study reassessing data collected after the COVID-19 pandemic.

Prevalence rates of overweight and obesity among children aged 3-5 years in the Bouches-du-Rhône department during the 2022-2023 school year: A cross-sectional study reassessing data collected after the COVID-19 pandemic.

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

Published: August 19, 2025

Tubeless automated insulin delivery versus multiple daily injections in children and adults with type 1 diabetes with elevated HbA1c (RADIANT): a multicentre, international, parallel-group, open-label, randomised, controlled trial.

Tubeless automated insulin delivery versus multiple daily injections in children and adults with type 1 diabetes with elevated HbA1c (RADIANT): a multicentre, international, parallel-group, open-label, randomised, controlled trial.

Journal: The lancet. Diabetes & endocrinology

Published: August 18, 2025

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

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Last Updated: 09/26/2026