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Citation: Ja. Ibdah et al., Molecular prenatal diagnosis in families with fetal mitochondrial trifunctional protein mutations, J PEDIAT, 138(3), 2001, pp. 396-399

Authors: Ibdah, JA Paul, H Zhao, Y Binford, S Salleng, K Cline, M Matern, D Bennett, MJ Rinaldo, P Strauss, AW

Citation: Ja. Ibdah et al., Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death, J CLIN INV, 107(11), 2001, pp. 1403-1409

Authors: Jones, PM Moffitt, M Joseph, D Harthcock, PA Boriack, RL Ibdah, JA 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: Ibdah, JA Yang, Z Bennett, MJ

Citation: Ja. Ibdah et al., Liver disease in pregnancy and fetal fatty acid oxidation defects, MOL GEN MET, 71(1-2), 2000, pp. 182-189

Authors: Ibdah, JA Dasouki, MJ Strauss, AW

Citation: Ja. Ibdah et al., Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Variable expressivity of maternal illness during pregnancy and unusual presentation with infantile cholestasis and hypocalcaemia, J INH MET D, 22(7), 1999, pp. 811-814

Authors: Ibdah, JA Bennett, MJ Rinaldo, P Zhao, YW Gibson, B Sims, HF Strauss, AW

Citation: Ja. Ibdah et al., A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women, N ENG J MED, 340(22), 1999, pp. 1723-1731