L. Smith

Expanded clinical and molecular spectrum of guanidinoacetate methyltransferase (GAMT) deficiency.

C. Eng, B. Maranda, F. Scaglia, 2009, Molecular genetics and metabolism.

Chronic infection phenotypes of Pseudomonas aeruginosa are associated with failure of eradication in children with cystic fibrosis

D. Hwang, D. Guttman, S. Clark, 2015, European Journal of Clinical Microbiology and Infectious Diseases.

The Effect of a New Calcium Channel Blocker (TA-3090) on Lipoprotein Profile and Intestinal Lipid Handling in Rodents

E. Levy, E. Seidman, L. Dumont, 1992, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

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.

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.

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.

Cisapride in pediatric gastroesophageal reflux.

R. Scott, C. Roy, H. Machida, 1997, Journal of pediatric gastroenterology and nutrition.

Chronic infection phenotypes of Pseudomonas aeruginosa are associated with failure of eradication in children with cystic fibrosis

D. Hwang, D. Guttman, S. Clark, 2015, European Journal of Clinical Microbiology & Infectious Diseases.

Liver disease in children with cystic fibrosis: US-biochemical comparison in 195 patients.

D. Filiatrault, H. Patriquin, C. Roy, 1999, Radiology.