Amikacin liposome inhalation suspension for chronic Pseudomonas aeruginosa infection in cystic fibrosis

Autor: Bilton D, Pressler T, Fajac I, Clancy JP, Sands D, Minic P, Cipolli M, Galeva I, Solé A, Quittner AL, Liu K, McGinnis JP, Eagle G, Gupta R, Konstan MW, CLEAR-108 Study Group

Publikováno v: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
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Shortcomings of inhaled antibiotic treatments for Pseudomonas aeruginosa infection in patients with cystic fibrosis (CF) include poor drug penetration, inactivation by sputum, poor efficiency due to protective biofilm, and short residence in the lung

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112 Analysis of long-term use of liposomal amikacin for inhalation (LAI) in patients with cystic fibrosis (CF) who have chronic infection from Pseudomonas aeruginosa

Autor: Bilton, D., Pressler, T., Fajac, I., Clancy, J.P., Minic, P., Cipolli, M., Galeva, I., Solé, A., Dupont, L.J., Mayer-Hamblett, N., Torchio, S., McGinnis, J.P., Eagle, G., Konstan, M.

Publikováno v: In Journal of Cystic Fibrosis June 2015 14 Supplement 1:S85-S85

293 Spectrum of mutations and survival data for adult CF patients from Sofia CF center

Autor: Galeva, I., Savov, A., Mileva, S., Yankova, M., Kabakchieva, R.

Publikováno v: In Journal of Cystic Fibrosis June 2014 13 Supplement 2:S123-S123

WS5.6 A challenging double-blind, placebo-controlled study of tobramycin inhalation powder in cystic fibrosis: results of the EDIT trial

Autor: Galeva, I., Konstan, M.W., Higgins, M., Piggott, S., Angyalosi, G., Brockhaus, F., Thomas, K., Chuchalin, A.G.

Publikováno v: In Journal of Cystic Fibrosis June 2012 11 Supplement 1:S12-S12

Allergen-specific immunoglobulin e antibodies in wheezing infants

Autor: Mileva, S., Galeva, I., Todor Popov

Publikováno v: Scopus-Elsevier

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