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Laurel S. Almer

Publications -  8
Citations -  529

Laurel S. Almer is an academic researcher. The author has contributed to research in topics: Ciprofloxacin & Staphylococcus aureus. The author has an hindex of 8, co-authored 8 publications receiving 511 citations.

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Fluoroquinolone Resistance in Streptococcus pneumoniae in United States since 1994-1995

TL;DR: Comparisons of the MIC frequency distributions of the study drugs against the isolates obtained during the three sampling periods encompassing this investigation revealed no evidence of changes in the in vitro activities of the fluoroquinolones.
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In Vitro Antibacterial Potency and Spectrum of ABT-492, a New Fluoroquinolone

TL;DR: The profile of ABT-492 suggested that it may be a useful agent for the treatment of community-acquired respiratory tract infections, as well as infections of the urinary tract, bloodstream, and skin and skin structure and nosocomial lung infections.
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Comparison of in vitro activities of ABT-773 and telithromycin against macrolide-susceptible and -resistant streptococci and staphylococci.

TL;DR: ABT-773 has superior activity against macrolide-resistant streptococci compared to that of telithromycin and lacks activity against constitutive macrolides-resistant Staphylococcus aureus but had good activities against inducibly resistant StaphlyococcusAureus.
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In Vitro and Bactericidal Activities of ABT-492, a Novel Fluoroquinolone, against Gram-Positive and Gram-Negative Organisms

TL;DR: ABT-492 was more potent against quinolone-susceptible and -resistant gram-positive organisms, had activity similar to that of ciprofloxacin against certain members of the family Enterobacteriaceae, and had comparable activity against quinolysis, nonfermentative, gram-negative organisms.
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Antimicrobial susceptibility and molecular characterization of community-acquired methicillin-resistant Staphylococcus aureus.

TL;DR: It is indicated that MRSA from adult subjects with community respiratory infections have similar antimicrobial susceptibility profiles and resistance mechanisms as nosocomial MRSA, and represent a genetically diverse group.