G. Lepage

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The potential of the hydrocarbon breath test as a measure of lipid peroxidation.

C. Kneepkens, G. Lepage, C. Roy, 1994, Free radical biology & medicine.

insufficiency in cystic fibrosis . malabsorption and pancreatic Relationship between bile acid

G. Lepage, C. Roy, A. Weber, 2006 .

Relationship between bile acid malabsorption and pancreatic insufficiency in cystic fibrosis.

G. Lepage, C. Roy, A. Weber, 1976, Gut.

Specific methylation of plasma nonesterified fatty acids in a one-step reaction.

G. Lepage, C. Roy, 1988, Journal of Lipid Research.

The composition of preterm milk in relation to the degree of prematurity

G. Lepage, C. Roy, P. Darling, 1984 .

Improved recovery of fatty acid through direct

G. Lepage, C. Roy, 1984 .

Bile formation and hepatic plasma membrane composition in guinea-pigs and rats.

F. Guertin, G. Lepage, C. Roy, 1995, Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.

Plasma and lipoprotein fatty acid composition in glycogen storage disease type I

E. Levy, G. Lepage, C. Roy, 1987, Lipids.

Beneficial effects of fish-oil supplements on lipids, lipoproteins, and lipoprotein lipase in patients with glycogen storage disease type I.

E. Levy, E. Seidman, J. Turgeon, 1993, The American journal of clinical nutrition.

Hyperlipoproteinemia in Glycogen Storage Disease Type I: Effect of Nocturnal Intragastric Feeding

E. Levy, E. Seidman, G. Lepage, 1988 .

Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.

H. Moser, A. Moser, C. Zeiss, 2002, American journal of human genetics.

The hydrocarbon breath test in the study of lipid peroxidation: principles and practice.

C. Kneepkens, G. Lepage, C. Roy, 1992, Clinical and investigative medicine. Medecine clinique et experimentale.

Intestinal apoB synthesis, lipids, and lipoproteins in chylomicron retention disease.

E. Levy, E. Seidman, Y. Marcel, 1987, Journal of lipid research.

20 HYDROCARBON BREATH TEST IN CYSTIC FIBROSIS: EVID‐ENCE FOR INCREASED LIPID PEROXIDATION

C. Kneepkens, G. Lepage, C. Roy, 1992, Journal of Pediatric Gastroenterology and Nutrition - JPGN.

Lipid abnormalities in pancreatic tissue of streptozotocin-induced diabetic rats

E. Levy, M. Bendayan, G. Lepage, 1988, Lipids.

Modulation of endoplasmic reticulum-bound cholesterol regulatory enzymes by iron/ascorbate-mediated lipid peroxidation.

E. Levy, E. Seidman, S. Brunet, 2000, Free radical biology & medicine.

Circulating lipids and lipoproteins in glycogen storage disease type I with nocturnal intragastric feeding.

E. Levy, M. Bendayan, G. Lepage, 1988, Journal of lipid research.

The Candida albicans phospholipomannan induces in vitro production of tumour necrosis factor-alpha from human and murine macrophages.

P. Trinel, D. Poulain, T. Jouault, 1994, Immunology.

Effect of Taurine Supplements on Fat Absorption in Cystic Fibrosis

G. Lepage, C. Roy, P. Darling, 1985, Pediatric Research.

Total Parenteral Nutrition in the Newborn: Energy Substrates and Plasma Total Fatty Acids

P. Chessex, S. Bisaillon, G. Lepage, 1989, Pediatric Research.

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.

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.

Combined (n-3 and n-6) essential fatty deficiency is a potent modulator of plasma lipids, lipoprotein composition, and lipolytic enzymes.

E. Levy, G. Lepage, C. Roy, 1990, Journal of lipid research.

Direct transesterification of all classes of lipids in a one-step reaction.

G. Lepage, C. Roy, 1986, Journal of lipid research.

Elemental diet improves steroid-dependent eosinophilic gastroenteritis and reverses growth failure.

E. Seidman, C. Justinich, G. Lepage, 1996, Journal of pediatric gastroenterology and nutrition.

Partially purified rabbit gastric lipase: in vitro and in vivo experiments to assess its potential contribution to gastric and intestinal lipolysis

Lesley J. Smith, E. Levy, J. Junien, 1991 .

Taurine Supplementation of a Premature Formula Improves Fat Absorption in Preterm Infants

N. Galeano, R. Giguere, G. Lepage, 1987, Pediatric Research.

Storage of medium-chain triglycerides in adipose tissue of orally fed infants.

P. Chessex, G. Lepage, C. Roy, 1987, The American journal of clinical nutrition.

Relationship of decreased hepatic lipase activity and lipoprotein abnormalities to essential fatty acid deficiency in cystic fibrosis patients.

E. Levy, N. Galeano, M. Bendayan, 1989, Journal of lipid research.

The role of gastric lipolysis on fat absorption and bile acid metabolism in the rat

M. Roulet, G. Lepage, C. Roy, 1979, Lipids.

Taurine decreases fecal fatty acid and sterol excretion in cystic fibrosis. A randomized double-blind trial.

G. Lepage, C. Roy, F. Lacaille, 1991, American journal of diseases of children.

Altered lipid profile, lipoprotein composition, and oxidant and antioxidant status in pediatric Crohn disease.

E. Levy, E. Seidman, S. Brunet, 2000, The American journal of clinical nutrition.

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.

Definitive chemical evidence for the constitutive ability of Candida albicans serotype A strains to synthesize β‐1,2 linked oligomannosides containing up to 14 mannose residues

G. Strecker, P. Trinel, D. Poulain, 1997, FEBS letters.

Beta-1,2-linked oligomannosides from Candida albicans act as signals for tumor necrosis factor alpha production

J. Wieruszeski, G. Strecker, P. Trinel, 1995, Infection and immunity.

Isolation andPreliminary Characterization ofthe14-to18- Kilodalton Candida albicans Antigen asa Phospholipomannan Containing 3-1,2-Linked Oligomannosides

P. Trinel, D. Poulain, T. Jouault, 1993 .

1H-NMR spectroscopy of manno-oligosaccharides of the beta-1,2-linked series released from the phosphopeptidomannan of Candida albicans VW-32 (serotype A).

J. Wieruszeski, G. Strecker, J. Michalski, 1991, Biochemical and biophysical research communications.

Uptake and metabolism of structured triglyceride by Caco-2 cells: reversal of essential fatty acid deficiency.

E. Levy, E. Seidman, G. Lepage, 1998, American journal of physiology. Gastrointestinal and liver physiology.

Improved recovery of fatty acid through direct transesterification without prior extraction or purification.

G. Lepage, C. Roy, G Lepage, 1984, Journal of lipid research.

The Influence of Taurine on the Bile Acid Maximum Secretory Rate in the Guinea Pig

D. Belli, G. Lepage, C. Roy, 1988, Pediatric Research.

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

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

S-adenosylmethionine prevents total parenteral nutrition-induced cholestasis in the rat.

D. Belli, G. Lepage, C. Roy, 1994, Journal of hepatology.

Total parenteral nutrition-associated cholestasis in rats: comparison of different amino acid mixtures.

D. Belli, G. Lepage, C. Roy, 1987, JPEN - Journal of Parenteral and Enteral Nutrition.

Liver Membrane Composition after Short-Term Parenteral Nutrition With and Without Taurine in Guinea Pigs: The Effect to Taurine

F. Guertin, G. Lepage, C. Roy, 1993, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Effect of taurine on total parenteral nutrition-associated cholestasis.

F. Guertin, R. Giguere, G. Lepage, 1991, JPEN. Journal of parenteral and enteral nutrition.

Surveillance for Cystic Fibrosis-Associated Hepatobiliary Disease: Early Ultrasound Changes and Predisposing Factors

N. Bureau, F. Harel, H. Patriquin, 2003, The Journal of pediatrics.

Essential fatty acid deficiency mimicking porphyria cutanea tarda in a patient with chronic cholestasis.

G. Lepage, J. Levy, A. Defelice, 1990, Journal of pediatric gastroenterology and nutrition.

Protein quality and quantity in preterm infants receiving the same energy intake.

G. Lepage, C. Roy, P. Darling, 1985, American journal of diseases of children.

The Influence of Ischemia-Reperfusion Injury on Plasma Malondialdehyde in Children Undergoing Cardiopulmonary Bypass

J. Lacroix, E. Delvin, S. Vobecky, 1998 .

A randomized trial of two levels of iron supplementation and developmental outcome in low birth weight infants.

J. Friel, M. L’Abbé, K. Aziz, 2001, The Journal of pediatrics.

Hepatobiliary disease in cystic fibrosis: a survey of current issues and concepts.

G. Lepage, C. Roy, G. Brisson, 1982, Journal of pediatric gastroenterology and nutrition.

The Effect of Lipids on Taurocholate Absorption from the Rat Small Intestine 1

G. Lepage, C. Roy, A. Weber, 1979, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Effect of dietary fat and residues on fecal loss of sterols and on their microbial degradation in cystic fibrosis

G. Lepage, C. Roy, C. Morin, 1986, Digestive Diseases and Sciences.

THE COMPOSITION OF PRETERM MILK IN RELATION TO THE DEGREE OF PREMATURITY

G. Lepage, C. Roy, P. Darling, 1984, Pediatric Research.

Effect of an organized lipid matrix on lipid absorption and clinical outcomes in patients with cystic fibrosis.

S. Chemtob, N. Bureau, D. Bérubé, 2002, The Journal of pediatrics.

Intraluminal and intracellular phases of fat absorption are impaired in essential fatty acid deficiency.

E. Levy, S. Dionne, G. Lepage, 1992, The American journal of physiology.

Fecal bile acids as a means of assessing the integrity of the enterohepatic circulation of bile acids and their microbial degradation.

G. Lepage, C. Roy, 1988, Journal of pediatric gastroenterology and nutrition.

Uptake and metabolism of structured triglyceride by Caco-2 cells: reversal of essential fatty acid deficiency.

E. Levy, E. Seidman, G. Lepage, 1998, The American journal of physiology.

Vulnerability of keto bile acids to alkaline hydrolysis.

G. Lepage, C. Roy, A. Fontaine, 1978, Journal of lipid research.

Increased levels of plasma malondialdehyde in Friedreich ataxia.

M. Emond, M. Pandolfo, M. Vanasse, 2000, Neurology.

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.

N-acetylcysteine in pig liver transplantation from non-heart-beating donors.

J. Lavoie, F. Proulx, G. Lepage, 1999, Transplantation.

Molecular cloning, expression analysis and iron metal cofactor characterisation of a superoxide dismutase from Toxoplasma gondii.

D. Dive, E. Viscogliosi, J. Renault, 2000, Molecular and biochemical parasitology.

2,3-Dinor-5,6-dihydro-15-F(2t)-isoprostane: a bioactive prostanoid metabolite.

J. Morrow, L. Roberts, X. Hou, 2001, American journal of physiology. Regulatory, integrative and comparative physiology.

Abnormal biliary lipid composition in cystic fibrosis. Effect of pancreatic enzymes.

A. Megevand, G. Lepage, C. Roy, 1977, The New England journal of medicine.

Taurine improves the absorption of a fat meal in patients with cystic fibrosis.

E. Levy, D. Belli, R. Giguere, 1987, Pediatrics.

Absence of pyridoxine-5'-phosphate oxidase (PNPO) activity in neoplastic cells: isolation, characterization, and expression of PNPO cDNA.

L. Nutter, E. Ngo, G. Lepage, 1998, Biochemistry.