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Journal of Pediatric Gastroenterology and Nutrition|March 22, 2019
Experience of Using a Semielemental Formula for Home Enteral Nutrition in Children: A Multicenter Cross-sectional StudyMarie Leonard, Dominique Caldari, Emmanuel Mas, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|December 17, 2022
A new 165-SNP low-density lipoprotein cholesterol polygenic risk score based on next generation sequencing outperforms previously published scores in routine diagnostics of familial hypercholesterolemiaXavier Vanhoye, Claire Bardel, Antoine Rimbert, et al.
Nutrition Research Reviews|September 29, 2025
Lipid intake in infants from birth to 3 years old: review of current guidelines and knowledge gapsNazek Najdi, Camille Jung, Eurídice Castañeda-Gutiérrez, et al.
Clinical Genetics|October 28, 2020
Development of a new expanded next-generation sequencing panel for genetic diseases involved in dyslipidemiaOriane Marmontel, Pierre Antoine Rollat-Farnier, Anne-Sophie Wozny, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 19, 2020
Phenotypic Differences Between Polygenic and Monogenic HypobetalipoproteinemiaAntoine Rimbert, Xavier Vanhoye, Dramane Coulibaly, et al.
Atherosclerosis|November 5, 2024
The singular French PCSK9-p.Ser127Arg gain-of-function variant: A significant player in cholesterol levels from a 775-year-old common ancestorYara Azar, Thomas E Ludwig, Hugo Le Bon, et al.
Science (New York, N.Y.)|February 23, 2023
Microbe-mediated intestinal NOD2 stimulation improves linear growth of undernourished infant miceMartin Schwarzer, Umesh Kumar Gautam, Kassem Makki, et al.
Journal of Hepatology|May 21, 2014
Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemiaMathilde Di Filippo, Philippe Moulin, Pascal Roy, et al.
Nutrients|June 24, 2022
Management of Central Venous Catheters in Children and Adults on Home Parenteral Nutrition: A French Survey of Current PracticeJulien Gotchac, Florian Poullenot, Dominique Guimber, et al.
Annales D'Endocrinologie|May 8, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditionsLaurence Faivre, Camille Level, Régis Coutant, et al.
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