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Clinical Nutrition Open Science|April 5, 2022
Undernourished patients do not have increased risk of severe COVID-19 outcomesAhmad Fneich, Pierre Poinsot, Christelle Elias, et al.
European Journal of Gastroenterology & Hepatology|January 28, 2005
IgA anti-transglutaminase antibodies as a tool for screening atypical forms of coeliac disease in a French at-risk paediatric populationWahiba Sakly, Françoise Bienvenu, Noël Peretti, et al.
European Journal of Endocrinology|August 18, 2006
Adiponutrin gene is regulated by insulin and glucose in human adipose tissueMarthe Moldes, Geneviève Beauregard, May Faraj, et al.
Journal of Clinical Lipidology|November 21, 2023
Carotenoids in familial hypobetalipoproteinemia disorders: Malabsorption in Caco2 cell models and severe deficiency in patientsClaire Bordat, Charlotte Cuerq, Charlotte Halimi, et al.
Pediatric Transplantation|January 12, 2016
Lipid profile and cardiovascular risk factors in pediatric liver transplant recipientsEmilie Roblin, Jérôme Dumortier, Mathilde Di Filippo, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 20, 2013
Inhibitory effects of in vivo oxidized high-density lipoproteins on platelet aggregation: evidence from patients with abetalipoproteinemiaCatherine Calzada, Evelyne Véricel, Romain Colas, et al.
Orphanet Journal of Rare Diseases|August 14, 2016
Establishment of reference values of α-tocopherol in plasma, red blood cells and adipose tissue in healthy children to improve the management of chylomicron retention disease, a rare genetic hypocholesterolemiaCharlotte Cuerq, Lioara Restier, Jocelyne Drai, et al.
Food & Function|February 22, 2012
Coupling in vitro gastrointestinal lipolysis and Caco-2 cell cultures for testing the absorption of different food emulsionsCécile Vors, Perrine Capolino, Clémence Guérin, et al.
Physiology & Behavior|February 11, 2017
Associations between food consumption patterns and saliva composition: Specificities of eating difficulties childrenMartine Morzel, Caroline Truntzer, Eric Neyraud, et al.
The Journal of Clinical Endocrinology and Metabolism|August 6, 2011
GPIHBP1 C89F neomutation and hydrophobic C-terminal domain G175R mutation in two pedigrees with severe hyperchylomicronemiaSybil Charrière, Noël Peretti, Sophie Bernard, et al.
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