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Journal of Inherited Metabolic Disease|January 1, 1985
Brain amino acid abnormalities in pyruvate carboxylase deficiencyT L Perry, J C Haworth, B H RobinsonProceedings of the National Academy of Sciences of the United States of America|April 1, 1972
Effects of palmitoyl CoA on citrate and malate transport by rat liver mitochondriaM L Halperin, B H Robinson, I B FritzCytometry|November 21, 2000
Simultaneous detection of mitochondrial respiratory chain activity and reactive oxygen in digitonin-permeabilized cells using flow cytometryN A Pham, B H Robinson, D W HedleyJournal of Inherited Metabolic Disease|January 5, 2002
A case of PDH-E1 alpha mosaicism in a male patient with severe metabolic lactic acidosisA Seyda, K Chun, S Packman, et al.American Journal of Human Genetics|September 1, 1985
Defective intramitochondrial NADH oxidation in skin fibroblasts from an infant with fatal neonatal lacticacidemiaB H Robinson, N McKay, P Goodyer, et al.Journal of Inherited Metabolic Disease|January 1, 1981
Lactic acidosis due to pyruvate carboxylase deficiencyJ C Haworth, B H Robinson, T L PerryHuman Molecular Genetics|April 18, 2000
Sequential deletion of C-terminal amino acids of the E(1)alpha component of the pyruvate dehydrogenase (PDH) complex leads to reduced steady-state levels of functional E(1)alpha(2)beta(2) tetramers: implications for patients with PDH deficiencyA Seyda, G McEachern, R Haas, et al.Proceedings of the National Academy of Sciences of the United States of America|May 13, 1997
The role of London forces in defining noncentrosymmetric order of high dipole moment-high hyperpolarizability chromophores in electrically poled polymeric thin filmsL R Dalton, A W Harper, B H RobinsonBiochimica Et Biophysica Acta|August 3, 1995
Macrocyclic lactone synthesis by lipases in water-in-oil microemulsionsG D Rees, B H Robinson, G R StephensonClinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1985
Immunoextraction of lipoamide dehydrogenase from cultured skin fibroblasts in patients with combined alpha-ketoacid dehydrogenase deficiencyG Otulakowski, W Nyhan, L Sweetman, et al.Pageof 21