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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.Bulletin of Mathematical Biology|February 6, 2010
Mathematical modelling of the Aux/IAA negative feedback loopA M Middleton, J R King, M J Bennett, et al.Biology of the Neonate|January 1, 1977
The development of glycolytic and pentose phosphate shunt enzymes in human brainM J Bennett, W R Timperley, C B Taylor, et al.Lipids|August 15, 2000
Gastroprotection of DNA with a synthetic cholic acid analogE J Niedzinski, M J Bennett, D C Olson, et al.Molecular Genetics and Metabolism|September 26, 2000
Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathwaysJ Vockley, P Rinaldo, M J Bennett, et al.Molecular Genetics and Metabolism|July 20, 2001
Impaired mitochondrial fatty acid oxidative flux in fibroblasts from a patient with malonyl-CoA decarboxylase deficiencyM J Bennett, P A Harthcock, R L Boriack, et al.Pageof 25