JeffreyCBrackettMD

PubMed

• 128 citations
  Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood.
  Arnold W. Strauss, Cynthia K. Powell, Daniel E. Hale, Melissa M. Anderson, Ajay Ahuja, Jeffrey C. Brackett, Harold F. Sims> ;Proceedings of the National Academy of Sciences of the United States of America. 1995 Nov 7
• 110 citations
  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, Rita C. Hoop, Jeffrey C. Brackett, Arnold W. Strauss, Edwin W. Naylor> ;Pediatric Research. 1995 May 1
• 76 citations
  Two alpha subunit donor splice site mutations cause human trifunctional protein deficiency.
  Jeffrey C. Brackett, H F Sims, Piero Rinaldo, S Shapiro, C. K. Powell, Michael J. Bennett, Arnold W. Strauss> ;The Journal of Clinical Investigation. 1995 May 1
• 67 citations
  Prognostic value of the signal-averaged electrocardiogram and a prolonged QRS in ischemic ana nonischemic cardiomyopathy
  Michael E. Silverman, Michael D. Pressel, Jeffrey C. Brackett, Salvatore S. Lauria, Michael R. Gold, Stephen S. Gottlieb> ;The American Journal of Cardiology. 1995 Mar 1
• 150 citations
  The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy
  Harold F. Sims, Jeffrey C. Brackett, Cynthia K. Powell, William R. Treem, Daniel E. Hale, Michael J. Bennett, Beverly Gibson, Scott Shapiro, Arnold W. Strauss> ;Proceedings of the National Academy of Sciences of the United States of America. 1995 Jan 31
• 30 citations
  A novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal death.
  Jeffrey C. Brackett, H F Sims, Robert D. Steiner, M Nunge, E M Zimmerman, B deMartinville, Piero Rinaldo, Rachel Slaugh, Arnold W. Strauss> ;The Journal of Clinical Investigation. 1994 Oct 1
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