1. Clinical Microbiology and Infection
Oral presentations 
Clinical Microbiology and Infection 
Volume 17, Pages S1-S107 (May 2011)
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2. Clinical Microbiology and Infection 2011 17, S1-S107DOI: (10. 1111/j
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3. Figure 1
In vivo activity of ClyS ointment vs. placebo or mupirocin on tape-stripped mice infected with S. aureus 8325–4 or MRSA MW2. Topical treatrnents included Aquaphor® (control), 10% ClyS binding domain in Aquaphor® (placebo), 10% wt/wt ClyS in Aquaphor®, and 2% mupirocin. The median value of the data for each group is shown as a horizontal bar; each sphere represents one mouse. No statistical significance was seen between untreated, control, and placebo groups. Statistical significance (p < ) was noted between untreated/control/placebo and ClyS groups with a three log drop in bacteria recovered (CFUs). Statistical difference (p = 0.001) was noted between ClyS and mupirocin treated groups, with a one log drop difference between them. Figure is representative of experiments using S. aureus strain 8325–4 or MRSA strain MW2.
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4. Fig. 1
Percent of cultures from the five high touch sites that were negative for aerobic growth after decontamination with the HPV and UVC process.
Clinical Microbiology and Infection  , S1-S107DOI: ( /j x)
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5. Clinical Microbiology and Infection 2011 17, S1-S107DOI: (10. 1111/j
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8. Figure 1
Implementation of policy elements covered by the survey questionnai re
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9. Clinical Microbiology and Infection 2011 17, S1-S107DOI: (10. 1111/j
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13. Figure 1
Pneumococcal vaccination and invasive pneumococcal disease 2002–2009.
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