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Clinical Biochemistry|December 1, 1978
Simple and rapid system for screening and identification of reducing sugars in urineC Auray-Blais, R Giguere, P Draper, et al.Clinical Biochemistry|August 1, 1980
An automated method for the determination of orotic acid in the urine of children being screened for metabolic disordersD Paradis, R Giguere, C Auray-Blais, et al.Journal of Inherited Metabolic Disease|January 1, 1986
Kinetic abnormalities of carbamyl phosphate synthetase-I in a case of congenital hyperammonaemiaI A Qureshi, J Letarte, R Ouellet, et al.Gastroenterology|January 1, 1988
Colonic hamartomas in tuberous sclerosisG Devroede, B Lemieux, S Massé, et al.The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1978
Platelet taurine uptake in spinocerebellar degenerationA Filla, R F Butterworth, G Geoffroy, et al.The Journal of Pediatrics|September 1, 1977
Dicarboxylic aminoaciduria: an inborn error of amino acid conservationS B Melançon, L Dallaire, B Lemieux, et al.The Plant Journal : for Cell and Molecular Biology|February 1, 1996
Molecular cloning and characterization of the CER2 gene of Arabidopsis thalianaV Negruk, P Yang, M Subramanian, et al.Journal of Inherited Metabolic Disease|January 1, 1983
A new French-Canadian family affected by hyperargininaemiaI A Qureshi, J Letarte, R Ouellet, et al.The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1978
Serum and platelet lipoamide dehydrogenase in Friedreich's ataxiaA Filla, R F Butterworth, G Geoffroy, et al.The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1979
Regulation of respiration in Friedreich's ataxiaR Begin, L Lupien, M A Bureau, et al.Pageof 11