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Philip D. Lister

Department of Medical Microbiology and Immunology

Creighton University School of Medicine

2500 California Plaza

Omaha

USA

[email]@creighton.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Medical Microbiology and Immunology, Creighton University School of Medicine, 2500 California Plaza, Omaha, USA. 2007 - 2009
  • Center for Research in Anti-Infectives and Biotechnology Department of Medical Microbiology and Immunology, Creighton University School of Medicine, Omaha, NE 68178, USA. 1998 - 2009

References

  1. Antibacterial-resistant Pseudomonas aeruginosa: clinical impact and complex regulation of chromosomally encoded resistance mechanisms. Lister, P.D., Wolter, D.J., Hanson, N.D. Clin. Microbiol. Rev. (2009) [Pubmed]
  2. Pharmacodynamics of levofloxacin against characterized ciprofloxacin-resistant Streptococcus pneumoniae. Lister, P.D. Postgrad. Med (2008) [Pubmed]
  3. Carbapenems in the USA: focus on doripenem. Lister, P.D. Expert. Rev. Anti. Infect. Ther (2007) [Pubmed]
  4. The role of pharmacodynamic research in the assessment and development of new antibacterial drugs. Lister, P.D. Biochem. Pharmacol. (2006) [Pubmed]
  5. Levofloxacin/imipenem prevents the emergence of high-level resistance among Pseudomonas aeruginosa strains already lacking susceptibility to one or both drugs. Lister, P.D., Wolter, D.J., Wickman, P.A., Reisbig, M.D. J. Antimicrob. Chemother. (2006) [Pubmed]
  6. Levofloxacin-imipenem combination prevents the emergence of resistance among clinical isolates of Pseudomonas aeruginosa. Lister, P.D., Wolter, D.J. Clin. Infect. Dis. (2005) [Pubmed]
  7. Pharmacodynamics of gatifloxacin against Streptococcus pneumoniae in an in vitro pharmacokinetic model: impact of area under the curve/MIC ratios on eradication. Lister, P.D. Antimicrob. Agents Chemother. (2002) [Pubmed]
  8. Pharmacodynamics of 750 mg and 500 mg doses of levofloxacin against ciprofloxacin-resistant strains of Streptococcus pneumoniae. Lister, P.D. Diagn. Microbiol. Infect. Dis. (2002) [Pubmed]
  9. Chromosomally-encoded resistance mechanisms of Pseudomonas aeruginosa: therapeutic implications. Lister, P.D. Am. J. Pharmacogenomics (2002) [Pubmed]
  10. Pharmacodynamics of moxifloxacin and levofloxacin against Staphylococcus aureus and Staphylococcus epidermidis in an in vitro pharmacodynamic model. Lister, P.D. Clin. Infect. Dis. (2001) [Pubmed]
  11. Pharmacodynamics of moxifloxacin, levofloxacin and sparfloxacin against Streptococcus pneumoniae. Lister, P.D., Sanders, C.C. J. Antimicrob. Chemother. (2001) [Pubmed]
  12. Clavulanate induces expression of the Pseudomonas aeruginosa AmpC cephalosporinase at physiologically relevant concentrations and antagonizes the antibacterial activity of ticarcillin. Lister, P.D., Gardner, V.M., Sanders, C.C. Antimicrob. Agents Chemother. (1999) [Pubmed]
  13. Pharmacodynamics of trovafloxacin, ofloxacin, and ciprofloxacin against Streptococcus pneumoniae in an in vitro pharmacokinetic model. Lister, P.D., Sanders, C.C. Antimicrob. Agents Chemother. (1999) [Pubmed]
  14. Pharmacodynamics of levofloxacin and ciprofloxacin against Streptococcus pneumoniae. Lister, P.D., Sanders, C.C. J. Antimicrob. Chemother. (1999) [Pubmed]
  15. Cefepime-aztreonam: a unique double beta-lactam combination for Pseudomonas aeruginosa. Lister, P.D., Sanders, W.E., Sanders, C.C. Antimicrob. Agents Chemother. (1998) [Pubmed]
 
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