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Bennett, MJ
Harthcock, PA
Boriack, RL
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Citation: Mj. Bennett et al., Impaired mitochondrial fatty acid oxidative flux in fibroblasts from a patient with malonyl-CoA decarboxylase deficiency, MOL GEN MET, 73(3), 2001, pp. 276-279
Authors:
Jones, PM
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Strauss, AW
Bennett, MJ
Citation: Pm. Jones et al., Accumulation of free 3-hydroxy fatty acids in the culture media of fibroblasts from patients deficient in long-chain L-3-hydroxyacyl-CoA dehydrogenase: A useful diagnostic aid, CLIN CHEM, 47(7), 2001, pp. 1190-1194
Authors:
Treacy, EP
Lambert, DM
Barnes, R
Boriack, RL
Vockley, J
O'Brien, LK
Jones, PM
Bennett, MJ
Citation: Ep. Treacy et al., Short-chain hydroxyacyl-coenzyme A dehydrogenase deficiency presenting as unexpected infant death: A family study, J PEDIAT, 137(2), 2000, pp. 257-259
Authors:
Jones, PM
Quinn, R
Fennessey, PV
Tjoa, S
Goodman, SI
Fiore, S
Burlina, AB
Rinaldo, P
Boriack, RL
Bennett, MJ
Citation: Pm. Jones et al., Improved stable isotope dilution-gas chromatography-mass spectrometry method for serum or plasma free 3-hydroxy-fatty acids and its utility for the study of disorders of mitochondrial fatty acid beta-oxidation, CLIN CHEM, 46(2), 2000, pp. 149-155
Authors:
Bennett, MJ
Spotswood, SD
Ross, KF
Comfort, S
Koonce, R
Boriack, RL
IJlst, L
Wanders, RJA
Citation: Mj. Bennett et al., Fatal hepatic short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: Clinical, biochemical, and pathological studies on three subjects withthis recently identified disorder of mitochondrial beta-oxidation, PEDIATR D P, 2(4), 1999, pp. 337-345
Authors:
Otto, LR
Boriack, RL
Marsh, DJ
Kum, JB
Eng, C
Burlina, AB
Bennett, MJ
Citation: Lr. Otto et al., Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (ERRS), AM J MED G, 83(1), 1999, pp. 3-5