Cyril Amouroux
Montpellier, France
Last Updated: 09/26/2026
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Found 24 publications
Surgical Morbidity and Short-Term Oncologic Status after Prophylactic-Intent Thyroidectomy in a Cohort of Children with MEN2 from the Multicenter GTE ENDOCAN-RENATEN Study.
Journal: Thyroid : official journal of the American Thyroid Association
Published: August 07, 2026
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
Genetic Heterogeneity Underlying Familial Short Stature.
Journal: Diagnostics (Basel, Switzerland)
Published: October 28, 2025
French national diagnosis and care protocol (PNDS) for infantile idiopathic hypercalcemia (IIH).
Journal: Orphanet journal of rare diseases
Published: April 10, 2025
Expanding the molecular spectrum of aggrecanopathies: exploring 24 patients with ACAN significant variants.
Journal: European journal of human genetics : EJHG
Published: March 13, 2025
Health-related quality of life in French pediatric patients with X-linked hypophosphatemia: real-world data from the International XLH Registry.
Journal: JBMR plus
Published: March 07, 2025
ENPP1 deficiency: almost ready for prime time!
Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Published: September 29, 2024
Endocrine management of transgender adolescents: Expert consensus of the french society of pediatric endocrinology and diabetology working group.
Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Published: August 02, 2024
Adult height improved over decades in patients with X-linked hypophosphatemia: a cohort study.
Journal: European journal of endocrinology
Published: April 21, 2023
Evaluation of the impact of pharmaceutical trainings and tools on the proper use of medicines in pediatrics.
Journal: Frontiers in pharmacology
Published: January 13, 2023
Association of Meier-Gorlin and microcephalic osteodysplastic primordial dwarfism type II clinical features in an individual with CDK5RAP2 primary microcephaly.
Journal: European journal of medical genetics
Published: November 24, 2022
A novel TBX19 gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical origin.
Journal: Frontiers in endocrinology
Published: October 26, 2022
Last Updated: 09/26/2026