Alain Carrie
Paris, France
Last Updated: 09/26/2026
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Found 53 publications
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions.
Journal: Annales d'endocrinologie
Published: May 08, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions.
Journal: Annales d'endocrinologie
Published: March 21, 2026
Preparedness and performance in pediatric assessment: linking OSCE, written exams, and training exposure in a two-year comparative study of medical students.
Journal: BMC medical education
Published: November 15, 2025
When simulation becomes physical: vicarious symptoms in standardized patients during osces.
Journal: BMC medical education
Published: June 11, 2025
Cardiometabolic risk in pseudohypertriglyceridemia resulting from hyperglycerolemia.
Journal: Journal of clinical lipidology
Published: February 09, 2025
Clinical Expression of Familial Hypercholesterolemia in Patients from France and French Canada Carrying Identical-by-Descent Pathogenic LDLR Gene Variants: A Proof-of-Concept Study.
Journal: Journal of clinical medicine
Published: August 26, 2024
The singular French PCSK9-p.Ser127Arg gain-of-function variant: A significant player in cholesterol levels from a 775-year-old common ancestor.
Journal: Atherosclerosis
Published: May 22, 2024
Additive Effect of APOE Rare Variants on the Phenotype of Familial Hypercholesterolemia.
Journal: Arteriosclerosis, thrombosis, and vascular biology
Published: May 02, 2023
Integrated omics approach for the identification of HDL structure-function relationships in PCSK9-related familial hypercholesterolemia.
Journal: Journal of clinical lipidology
Published: February 24, 2023
Maternal Inheritance of Familial Hypercholesterolemia Gene Mutation Predisposes to Coronary Atherosclerosis as Assessed by Calcium Score in Adulthood.
Journal: Arteriosclerosis, thrombosis, and vascular biology
Published: December 29, 2022
Last Updated: 09/26/2026