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J T Clarke

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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 Bier
Biochimica 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 Mulcahey
Clinical Chemistry|November 1, 1992
Rapid nonradioactive tracer method for detecting carriers of the major Ashkenazi Jewish Tay-Sachs disease mutationsP M Strasberg, J T Clarke
Critical Reviews in Clinical Laboratory Sciences|January 1, 1995
Organic acidurias and related abnormalitiesD C Lehotay, J T Clarke
CMAJ : 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 Clarke
Science (New York, N.Y.)|May 21, 1993
Deceleration of interstellar hydrogen at the heliospheric interfaceR Lallement, J L Bertaux, J T Clarke
Clinical Biochemistry|June 1, 1987
Maternal phenylketonuria (PKU)--a reviewW B Hanley, J T Clarke, W Schoonheyt
Journal of Child Neurology|September 1, 1995
Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathyC L Pridmore, J T Clarke, S Blaser
The Journal of Pediatrics|November 1, 1993
Copper-histidine therapy for Menkes diseaseB Sarkar, K Lingertat-Walsh, J T Clarke
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|September 21, 2001
Managing public payment for high-cost, high-benefit treatment: enzyme replacement therapy for Gaucher's disease in OntarioJ T Clarke, D Amato, R B Deber
Pageof 16

Showing results (21-30 of 155) with videos related to

Sort By:
Pageof 16
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 Bier
Biochimica 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 Mulcahey
Clinical Chemistry|November 1, 1992
Rapid nonradioactive tracer method for detecting carriers of the major Ashkenazi Jewish Tay-Sachs disease mutationsP M Strasberg, J T Clarke
Critical Reviews in Clinical Laboratory Sciences|January 1, 1995
Organic acidurias and related abnormalitiesD C Lehotay, J T Clarke
CMAJ : 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 Clarke
Science (New York, N.Y.)|May 21, 1993
Deceleration of interstellar hydrogen at the heliospheric interfaceR Lallement, J L Bertaux, J T Clarke
Clinical Biochemistry|June 1, 1987
Maternal phenylketonuria (PKU)--a reviewW B Hanley, J T Clarke, W Schoonheyt
Journal of Child Neurology|September 1, 1995
Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathyC L Pridmore, J T Clarke, S Blaser
The Journal of Pediatrics|November 1, 1993
Copper-histidine therapy for Menkes diseaseB Sarkar, K Lingertat-Walsh, J T Clarke
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|September 21, 2001
Managing public payment for high-cost, high-benefit treatment: enzyme replacement therapy for Gaucher's disease in OntarioJ T Clarke, D Amato, R B Deber
Pageof 16