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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.American Journal of Medical Genetics|August 1, 1994
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (L-CHAD) deficiency in a patient with the Bannayan-Riley-Ruvalcaba syndromeJ S Fryburg, J P Pelegano, M J Bennett, et al.Ear and Hearing|November 1, 1985
Ipsilateral and contralateral acoustic reflexes in neonatesP M McMillan, M J Bennett, C D Marchant, et al.Developmental Medicine and Child Neurology|July 1, 1994
Juvenile neuronal ceroid-lipofuscinosis: developmental progress after supplementation with polyunsaturated fatty acidsM J Bennett, A R Gayton, C D Rittey, et al.Pageof 35