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Metabolism: Clinical and Experimental|October 1, 1982
The conversion of phenylalanine to tyrosine in man. Direct measurement by continuous intravenous tracer infusions of L-[ring-2H5]phenylalanine and L-[1-13C] tyrosine in the postabsorptive stateJ T Clarke, D M BierBiochimica Et Biophysica Acta|July 20, 1976
Cytidine-5'-monophospho-N-acetylneuraminic acid galactosyl-N-acetylgalactosaminyl-(N-acetylneuraminyl)-galactosyl-glucosylceramide sialyltransferase in the neurohypophysis of the rabbitJ T Clarke, M R MulcaheyClinical Chemistry|November 1, 1992
Rapid nonradioactive tracer method for detecting carriers of the major Ashkenazi Jewish Tay-Sachs disease mutationsP M Strasberg, J T ClarkeCritical Reviews in Clinical Laboratory Sciences|January 1, 1995
Organic acidurias and related abnormalitiesD C Lehotay, J T ClarkeCMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|December 23, 1998
Enzyme replacement therapy for Gaucher's disease: the early Canadian experienceJ J MacKenzie, D Amato, J T ClarkeScience (New York, N.Y.)|May 21, 1993
Deceleration of interstellar hydrogen at the heliospheric interfaceR Lallement, J L Bertaux, J T ClarkeClinical Biochemistry|June 1, 1987
Maternal phenylketonuria (PKU)--a reviewW B Hanley, J T Clarke, W SchoonheytJournal of Child Neurology|September 1, 1995
Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathyC L Pridmore, J T Clarke, S BlaserThe Journal of Pediatrics|November 1, 1993
Copper-histidine therapy for Menkes diseaseB Sarkar, K Lingertat-Walsh, J T ClarkeAmerican Journal of Medical Genetics|December 1, 1989
Tay-Sachs disease carrier screening: follow-up of a case-finding approachJ T Clarke, M A Skomorowski, S ZukerPageof 13