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The Journal of Membrane Biology|November 2, 2013
Inhibitors of the dicarboxylate and tricarboxylate transporting systems of rat liver mitochondriaB H Robinson, G R Williams, M L Halperin, et al.
Alcohol (Fayetteville, N.Y.)|October 23, 2001
Impairment of pyruvate dehydrogenase activity by acetaldehydeM L Hard, S Raha, M Spino, et al.
International Journal of Phytoremediation|January 31, 2004
Nickel and cobalt phytoextraction by the hyperaccumulator Berkheya coddii: implications for polymetallic phytomining and phytoremediationS M Keeling, R B Stewart, C W Anderson, et al.
Archives of Neurology|September 1, 1988
In utero central nervous system damage in pyruvate dehydrogenase deficiencyK A Aleck, A M Kaplan, W G Sherwood, et al.
The Journal of Pediatrics|February 1, 1987
Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: clues to pathogenesis of Leigh diseaseB H Robinson, L De Meirleir, M Glerum, et al.
Biochemical and Biophysical Research Communications|July 29, 1994
cDNA cloning of human kidney pyruvate carboxylaseN MacKay, B Rigat, C Douglas, et al.
American Journal of Diseases of Children (1960)|March 1, 1978
Nocturnal intragastric infusion of glucose in management of defective gluconeogenesis with hypoglycemiaR M Ehrlich, B H Robinson, M H Freedman, et al.
Biochemical Medicine and Metabolic Biology|October 1, 1992
Nonviability of cells with oxidative defects in galactose medium: a screening test for affected patient fibroblastsB H Robinson, R Petrova-Benedict, J R Buncic, et al.
Clinical Endocrinology|December 1, 1977
Spinal calcium changes with 1alpha-hydroxyvitamin D3J T Dabek, B H Robinson, R B Naik, et al.
European Journal of Pediatrics|May 1, 1993
An unusual patient with the neonatal Marfan phenotype and mitochondrial complex I deficiencyJ Christodoulou, R Petrova-Benedict, B H Robinson, et al.
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