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Antimicrobial Agents and Chemotherapy|May 20, 2009
Pharmacokinetic and pharmacodynamic evaluation of liposomal amikacin for inhalation in cystic fibrosis patients with chronic pseudomonal infectionOlanrewaju O Okusanya, Sujata M Bhavnani, Jeffrey Hammel, et al.Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|July 10, 2007
Comparison of the efficacy and safety of ciclesonide 160 microg once daily vs. budesonide 400 microg once daily in children with asthmaAndrea von Berg, Renate Engelstätter, Predrag Minic, et al.Plos One|October 10, 2018
Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variantsMarina Andjelkovic, Predrag Minic, Misa Vreca, et al.Journal of Clinical Immunology|February 1, 2014
Severe combined immunodeficiency in Serbia and Montenegro between years 1986 and 2010: a single-center experienceSrdjan Pasic, Dragana Vujic, Dobrila Veljković, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 19, 2021
Long-term amikacin liposome inhalation suspension in cystic fibrosis patients with chronic P. aeruginosa infectionDiana Bilton, Isabelle Fajac, Tacjana Pressler, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 28, 2019
Amikacin liposome inhalation suspension for chronic Pseudomonas aeruginosa infection in cystic fibrosisDiana Bilton, Tacjana Pressler, Isabelle Fajac, et al.Pageof 3