Claude C. Roy

Ursodeoxycholic acid improves the hepatic metabolism of essential fatty acids and retinol in children with cystic fibrosis.

G. Lepage, C. Roy, F. Lacaille, 1997, The Journal of pediatrics.

Direct transesterification of plasma fatty acids for the diagnosis of essential fatty acid deficiency in cystic fibrosis.

E. Levy, N. Galeano, G. Lepage, 1989, Journal of lipid research.

Lipoprotein abnormalities associated with cholesteryl ester transfer activity in cystic fibrosis patients: the role of essential fatty acid deficiency.

E. Levy, M. Lambert, G. Lepage, 1993, The American journal of clinical nutrition.

Absence of intestinal synthesis of apolipoprotein B-48 in two cases of abetalipoproteinemia.

E. Levy, Y. Marcel, R. Milne, 1987, Gastroenterology.

In vitro remodelling of plasma lipoproteins in whole plasma by lipoprotein lipase in primary and secondary hypertriglyceridaemia

E. Levy, E. Seidman, T. Olivecrona, 1990, European journal of clinical investigation.

Preparative steps necessary for the accurate measurement of malondialdehyde by high-performance liquid chromatography.

G. Lepage, J. Champagne, G. Munoz, 1991, Analytical biochemistry.

Supplementation with carotenoids corrects increased lipid peroxidation in children with cystic fibrosis.

R. Sokol, I. Osberg, G. Lepage, 1996, The American journal of clinical nutrition.

Short-chain fatty acids: ready for prime time?

E. Levy, C. L. Kien, C. Roy, 2006, Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition.