Absolute Bioavailability and Intracellular Pharmacokinetics of Azithromycin in Patients with Cystic Fibrosis

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Veröffentlicht in:Antimicrobial Agents and Chemotherapy 2005-12, Vol.49 (12), p.5013-5017
Hauptverfasser: BERINGER, Paul, MY TU HUYNH, Kitty, SHAPIRO, Bertrand, GILL, Mark, KRIENGKAUYKIAT, Jane, LUKE BI, HOEM, Nils, LOUIE, Stan, HAN, Emily, NGUYEN, Thao, HSU, Donald, RAO, Purush A
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container_end_page 5017
container_issue 12
container_start_page 5013
container_title Antimicrobial Agents and Chemotherapy
container_volume 49
creator BERINGER, Paul
MY TU HUYNH, Kitty
SHAPIRO, Bertrand
GILL, Mark
KRIENGKAUYKIAT, Jane
LUKE BI
HOEM, Nils
LOUIE, Stan
HAN, Emily
NGUYEN, Thao
HSU, Donald
RAO, Purush A
description Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue AAC About AAC Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy AAC RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0066-4804 Online ISSN: 1098-6596 Copyright © 2014 by the American Society for Microbiology.   For an alternate route to AAC .asm.org, visit: AAC       
doi_str_mv 10.1128/AAC.49.12.5013-5017.2005
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source MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Adult
Antibiotics. Antiinfectious agents. Antiparasitic agents
Azithromycin
Azithromycin - pharmacokinetics
Azithromycin - therapeutic use
Biological and medical sciences
Biological Availability
Cross-Over Studies
Cystic Fibrosis
Cystic Fibrosis - drug therapy
Cystic Fibrosis - metabolism
Errors of metabolism
Humans
Medical sciences
Metabolic diseases
Miscellaneous hereditary metabolic disorders
Pancreas - enzymology
Pharmacology
Pharmacology. Drug treatments
Pseudomonas aeruginosa
title Absolute Bioavailability and Intracellular Pharmacokinetics of Azithromycin in Patients with Cystic Fibrosis
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