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Prenatal Diagnosis|August 1, 1991
Prenatal diagnosis of fetal anomalies during the second trimester of pregnancy: their characterization and delineation of defects in pregnancies at riskL Dallaire, J Michaud, S B Melancon, et al.
Human Mutation|May 29, 1998
Molecular pathology of galactosialidosis in a patient affected with two new frameshift mutations in the cathepsin A/protective protein geneC Richard, J Tranchemontagne, M A Elsliger, et al.
Biochimica Et Biophysica Acta|June 24, 1991
Identification and localization of ATP-diphosphohydrolase (apyrase) in bovine aorta: relevance to vascular tone and platelet aggregationY P Côté, M Picher, P St-Jean, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 3, 1979
Neuraminidase activity in the mucolipidoses (types I, II and III) and the cherry-red spot myoclonus syndromeM Potier, G Beauregard, M Bélisle, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1982
Oral lecithin and linoleic acid in Friedreich's ataxia: III. Biochemical resultsS B Melancon, L Dallaire, M Potier, et al.
Cytokine|March 8, 2000
Renal synthesis of leukaemia inhibitory factor (LIF), under normal and inflammatory conditionsD S Morel, J L Taupin, M Potier, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1978
Lipoamide dehydrogenase in Friedreich's ataxia fibroblastsS B Melançon, M Potier, L Dallaire, et al.
Transplantation|September 6, 2000
Matrix accumulation in mesangial cells exposed to cyclosporine A requires a permissive genetic backgroundA Fornoni, O Lenz, I Tack, et al.
Gastroenterology|March 1, 1994
Diarrhea and autonomic dysfunction in a patient with hexosaminidase B deficiency (Sandhoff disease)R Modigliani, M Lemann, S B Melançon, et al.
The Biochemical Journal|December 15, 1987
Altered molecular size of N-acetylglucosamine 1-phosphotransferase in I-cell disease and pseudo-Hurler polydystrophyY Ben-Yoseph, M Potier, D A Mitchell, et al.
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