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Molecular Genetics and Metabolism|April 18, 2000
Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiencyB Z Yang, J H Ding, C Zhou, et al.Biopharmaceutics & Drug Disposition|March 1, 1987
Single intravenous dose and steady-state oral dose pharmacokinetics of nicardipine in healthy subjectsJ G Wagner, T L Ling, E J Mroszczak, et al.Biochemical and Biophysical Research Communications|October 26, 1999
Identification of two novel mutations in the hypoglycemic phenotype of very long chain acyl-CoA dehydrogenase deficiencyG He, B Z Yang, D S Roe, et al.Annals of Neurology|October 1, 1977
Pedigree testing in Duchenne muscular dystrophyA D Roses, M J Roses, B S Metcalf, et al.Journal of Inherited Metabolic Disease|January 1, 1990
Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiencyM J Bennett, P M Coates, D E Hale, et al.Pediatrics|February 1, 1989
Acute profound dystonia in infants with glutaric acidemiaI Bergman, D Finegold, J C Gartner, et al.Pediatric Research|January 1, 1994
Intravenous L-carnitine and acetyl-L-carnitine in medium-chain acyl-coenzyme A dehydrogenase deficiency and isovaleric acidemiaJ L Van Hove, S G Kahler, D S Millington, et al.Kidney International|February 1, 1997
Structural and functional analysis of hypoxia-inducible factor 1G L Semenza, F Agani, G Booth, et al.The Journal of Clinical Investigation|May 1, 1990
2,4-Dienoyl-coenzyme A reductase deficiency: a possible new disorder of fatty acid oxidationC R Roe, D S Millington, D L Norwood, et al.Prenatal Diagnosis|December 18, 2001
Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: association with elevated alpha-fetoprotein and cystic renal changesC A Chisholm, F Vavelidis, M A Lovell, et al.Pageof 18