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American Journal of Physiology. Endocrinology and Metabolism|April 26, 2000
Utilization of very low density lipoprotein by rat heart: the effect of endotoxinM J Bennett, D Hauton, D G Hole, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|December 8, 2021
Utilisation of CO<sub>2</sub> as "Structure Modifier" of Inorganic SolidsM J Bennett, I Dobson, D M Benoit, et al.The Journal of Pediatrics|January 1, 1993
Limitations of 3-phenylpropionylglycine in early screening for medium-chain acyl-coenzyme A dehydrogenase deficiencyA Bhala, M J Bennett, K L McGowan, et al.Clinical Chemistry|October 1, 1994
Tiglylglycine excreted in urine in disorders of isoleucine metabolism and the respiratory chain measured by stable isotope dilution GC-MSM J Bennett, S Powell, D J Swartling, et al.Annals of Clinical Biochemistry|September 1, 1992
Comparison of post-mortem urinary and vitreous humour organic acidsM J Bennett, M C Ragni, I Hood, et al.Radiology|December 1, 1990
Mucocele of the cystic duct remnant in eight liver transplant recipients: findings at cholangiography, CT, and USA B Zajko, M J Bennett, W L Campbell, et al.Lancet (London, England)|December 16, 1978
Some problems of alpha-fetoprotein screeningM J Bennett, K Blau, R D Johnson, et al.The Journal of Pediatrics|January 1, 1995
Transient organic aciduria and persistent lacticacidemia in a patient with short-chain acyl-coenzyme A dehydrogenase deficiencyD B Dawson, L Waber, D E Hale, et al.The Journal of Pediatrics|April 17, 1998
3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their childrenK M Gibson, M J Bennett, E W Naylor, et al.Journal of Inherited Metabolic Disease|January 1, 1996
Late-onset holocarboxylase synthetase deficiencyK M Gibson, M J Bennett, W L Nyhan, et al.Pageof 25