Barbara Girerd
Paris, France
Last Updated: 09/26/2026
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Found 91 publications
Integrating genetic counseling in endocrine practice: Prevention, reproductive care, and prenatal diagnosis.
Journal: Annales d'endocrinologie
Published: March 21, 2026
Splenic structural and functional abnormalities in individuals with NR5A1/SF-1 variants.
Journal: Endocrine connections
Published: August 23, 2025
Burosumab prevents further height deficit in toddlers affected by XLH.
Journal: Endocrine connections
Published: July 15, 2025
French national diagnosis and care protocol (PNDS) for infantile idiopathic hypercalcemia (IIH).
Journal: Orphanet journal of rare diseases
Published: April 10, 2025
Adult height improved over decades in patients with X-linked hypophosphatemia: a cohort study.
Journal: European journal of endocrinology
Published: April 21, 2023
First Genotype-Phenotype Study in TBX4 Syndrome: Gain-of-Function Mutations Causative for Lung Disease.
Journal: American journal of respiratory and critical care medicine
Published: July 19, 2022
Screening for pulmonary veno-occlusive disease in heterozygous EIF2AK4 variant carriers.
Journal: The European respiratory journal
Published: April 12, 2022
Mining the Plasma Proteome for Insights into the Molecular Pathology of Pulmonary Arterial Hypertension.
Journal: American journal of respiratory and critical care medicine
Published: April 08, 2022
An emerging phenotype of pulmonary arterial hypertension patients carrying SOX17 variants.
Journal: The European respiratory journal
Published: March 28, 2022
French clinical practice guidelines for the diagnosis and management of lung disease with alpha 1-antitrypsin deficiency
Journal: Revue des maladies respiratoires
Published: March 09, 2022
SUR1 As a New Therapeutic Target for Pulmonary Arterial Hypertension.
Journal: American journal of respiratory cell and molecular biology
Published: February 17, 2022
Last Updated: 09/26/2026