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The American Journal of Cardiology|March 1, 1995
Prognostic value of the signal-averaged electrocardiogram and a prolonged QRS in ischemic and nonischemic cardiomyopathyM E Silverman, M D Pressel, J C Brackett, et al.The Journal of Clinical Investigation|May 1, 1995
Two alpha subunit donor splice site mutations cause human trifunctional protein deficiencyJ C Brackett, H F Sims, P Rinaldo, et al.Pediatric Research|May 1, 1995
Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequenciesR Ziadeh, E P Hoffman, D N Finegold, et al.Proceedings of the National Academy of Sciences of the United States of America|November 7, 1995
Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhoodA W Strauss, C K Powell, D E Hale, et al.The Journal of Clinical Investigation|October 1, 1994
A novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal deathJ C Brackett, H F Sims, R D Steiner, et al.Proceedings of the National Academy of Sciences of the United States of America|January 31, 1995
The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancyH F Sims, J C Brackett, C K Powell, et al.Pageof 1