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Your search keyword '"Donnelly, J Peter"' showing total 15 results
Start Over Author "Donnelly, J Peter" Publisher american society for microbiology
15 results on '"Donnelly, J Peter"'

1. Comparison of Nonculture Blood-Based Tests for Diagnosing Invasive Aspergillosis in an Animal Model

Author

White, P. Lewis, primary, Wiederhold, Nathan P., additional, Loeffler, Juergen, additional, Najvar, Laura K., additional, Melchers, Willem, additional, Herrera, Monica, additional, Bretagne, Stephane, additional, Wickes, Brian, additional, Kirkpatrick, William R., additional, Barnes, Rosemary A., additional, Donnelly, J. Peter, additional, and Patterson, Thomas F., additional

Published
2016
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2. Analytical Comparison of In Vitro -Spiked Human Serum and Plasma for PCR-Based Detection of Aspergillus fumigatus DNA: a Study by the European Aspergillus PCR Initiative

Author

Loeffler, Juergen, primary, Mengoli, Carlo, additional, Springer, Jan, additional, Bretagne, Stéphane, additional, Cuenca-Estrella, Manuel, additional, Klingspor, Lena, additional, Lagrou, Katrien, additional, Melchers, Willem J. G., additional, Morton, C. Oliver, additional, Barnes, Rosemary A., additional, Donnelly, J. Peter, additional, and White, P. Lewis, additional

Published
2015
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3. Clinical Performance of Aspergillus PCR for Testing Serum and Plasma: a Study by the European Aspergillus PCR Initiative

Author

White, P. Lewis, primary, Barnes, Rosemary A., additional, Springer, Jan, additional, Klingspor, Lena, additional, Cuenca-Estrella, Manuel, additional, Morton, C. Oliver, additional, Lagrou, Katrien, additional, Bretagne, Stéphane, additional, Melchers, Willem J. G., additional, Mengoli, Carlo, additional, Donnelly, J. Peter, additional, Heinz, Werner J., additional, and Loeffler, Juergen, additional

Published
2015
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5. Evaluation of Aspergillus PCR Protocols for Testing Serum Specimens

Author

White, P. Lewis, primary, Mengoli, Carlo, additional, Bretagne, Stéphane, additional, Cuenca-Estrella, Manuel, additional, Finnstrom, Niklas, additional, Klingspor, Lena, additional, Melchers, Willem J. G., additional, McCulloch, Elaine, additional, Barnes, Rosemary A., additional, Donnelly, J. Peter, additional, and Loeffler, Juergen, additional

Published
2011
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7. Aspergillus PCR: One Step Closer to Standardization

Author

White, P. Lewis, primary, Bretagne, Stéphane, additional, Klingspor, Lena, additional, Melchers, Willem J. G., additional, McCulloch, Elaine, additional, Schulz, Bettina, additional, Finnstrom, Niklas, additional, Mengoli, Carlo, additional, Barnes, Rosemary A., additional, Donnelly, J. Peter, additional, and Loeffler, Juergen, additional

Published
2010
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12. Statistical Analyses of Correlation between Fluconazole MICs for Candida spp. Assessed by Standard Methods Set Forth by the European Committee on Antimicrobial Susceptibility Testing (E.Dis. 7.1) and CLSI (M27-A2)

Author

Rodriguez-Tudela, Juan Luis, primary, Donnelly, J. Peter, additional, Pfaller, Michael A., additional, Chryssantou, Erja, additional, Warn, Peter, additional, Denning, David W., additional, Espinel-Ingroff, Ana, additional, Barchiesi, Francesco, additional, and Cuenca-Estrella, Manuel, additional

Published
2007
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14. Development and evaluation of a calibrator material for nucleic acid-based assays for diagnosing aspergillosis.

Author

Lyon GM, Abdul-Ali D, Loeffler J, White PL, Wickes B, Herrera ML, Alexander BD, Baden LR, Clancy C, Denning D, Nguyen MH, Sugrue M, Wheat LJ, Wingard JR, Donnelly JP, Barnes R, Patterson TF, and Caliendo AM

Subjects
Humans, Microbiological Techniques methods, Molecular Diagnostic Techniques methods, Aspergillosis diagnosis, Aspergillus genetics, DNA, Fungal genetics, Microbiological Techniques standards, Molecular Diagnostic Techniques standards, Reference Standards
Abstract

Twelve laboratories evaluated candidate material for an Aspergillus DNA calibrator. The DNA material was quantified using limiting-dilution analysis; the mean concentration was determined to be 1.73 × 10(10) units/ml. The calibrator can be used to standardize aspergillosis diagnostic assays which detect and/or quantify nucleic acid.

Published
2013
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15. In vitro activities of new and conventional antifungal agents against clinical Scedosporium isolates.

Author

Meletiadis J, Meis JF, Mouton JW, Rodriquez-Tudela JL, Donnelly JP, and Verweij PE

Subjects
Humans, Miconazole pharmacology, Microbial Sensitivity Tests, Nystatin pharmacology, Scedosporium isolation & purification, Antifungal Agents pharmacology, Scedosporium drug effects
Abstract

The susceptibilities of 13 clinical isolates of Scedosporium apiospermum and 55 clinical isolates of S. prolificans to new and conventional drugs belonging to three different classes of antifungal agents, the azoles (miconazole, itraconazole, voriconazole, UR-9825, posaconazole), the polyenes (amphotericin B, nystatin and liposomal nystatin), and allylamines (terbinafine), were studied by use of proposed standard M38-P of NCCLS. Low growth-inhibitory antifungal activities were found in vitro for most of the drugs tested against S. prolificans isolates, with the MICs at which 90% of isolates are inhibited (MIC(90)s) being >8 microg/ml; the MIC(90)s of voriconazole and UR-9825, however, were 4 microg/ml. S. apiospermum isolates were more susceptible in vitro, with the highest activity exhibited by voriconazole (MIC(90)s, 0.5 microg/ml), followed by miconazole (MIC(90)s, 1 microg/ml), UR-9825 and posaconazole (MIC(90)s, 2 microg/ml), and itraconazole (MIC(90)s, 4 microg/ml). The MICs of terbinafine, amphotericin B, and the two formulations of nystatin (for which no statistically significant differences in antifungal activities were found for the two species) for S. apiospermum isolates were high. Cross-resistance was observed among all the azoles except posaconazole and among all the polyenes except the lipid formulation. A distribution analysis was performed with the MICs of each drug and for each species. Bimodal and skewed MIC distributions were obtained, and cutoffs indicating the borders of different MIC subpopulations of the distributions were determined on the basis of the normal plot technique. These cutoffs were in many cases reproducible between 48 and 72 h.

Published
2002
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