J C Brackett

The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy.

Harold F. Sims, J C Brackett, C K Powell et al. · Proceedings of the National Academy of Sciences · 1995 · 221 citations · Full text

Metabolic Disorder, Genetics, Fetal Health +25

Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood.

Arnold W. Strauss, C K Powell, Daniel E. Hale et al. · Proceedings of the National Academy of Sciences · 1995 · 168 citations · Full text

Medium Chain Acyl-CoA Dehydrogenase Deficiency in Pennsylvania: Neonatal Screening Shows High Incidence and Unexpected Mutation Frequencies

Rana Ziadeh, Eric P. Hoffman, David N. Finegold et al. · Pediatric Research · 1995 · 167 citations · Full text

Unexpected Mutation Frequencies, Genetic Disorder, Genetics +7

Prognostic value of the signal-averaged electrocardiogram and a prolonged QRS in ischemic ana nonischemic cardiomyopathy

Michael E. Silverman, Michael D. Pressel, J C Brackett et al. · The American Journal of Cardiology · 1995 · 100 citations

Cardiomyopathy, Heart Failure, Electrophysiological Evaluation +11

Two alpha subunit donor splice site mutations cause human trifunctional protein deficiency.

J C Brackett, Harold F. Sims, Piero Rinaldo et al. · Journal of Clinical Investigation · 1995 · 100 citations · Full text

Beta Subunits, Transcriptional Regulation, Systems Biology +13