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Items: 1 to 20 of 62

1.

Insights into the cystic fibrosis care in Eastern Europe: Results of survey.

Walicka-Serzysko K, Peckova M, Noordhoek JJ, Sands D, Drevinek P.

J Cyst Fibros. 2018 Apr 19. pii: S1569-1993(18)30088-2. doi: 10.1016/j.jcf.2018.04.003. [Epub ahead of print]

PMID:
29681443
2.

ECFS best practice guidelines: the 2018 revision.

Castellani C, Duff AJA, Bell SC, Heijerman HGM, Munck A, Ratjen F, Sermet-Gaudelus I, Southern KW, Barben J, Flume PA, Hodková P, Kashirskaya N, Kirszenbaum MN, Madge S, Oxley H, Plant B, Schwarzenberg SJ, Smyth AR, Taccetti G, Wagner TOF, Wolfe SP, Drevinek P.

J Cyst Fibros. 2018 Mar;17(2):153-178. doi: 10.1016/j.jcf.2018.02.006. Epub 2018 Mar 3. Review.

3.

What matters in chronic Burkholderia cenocepacia infection in cystic fibrosis: Insights from comparative genomics.

Nunvar J, Capek V, Fiser K, Fila L, Drevinek P.

PLoS Pathog. 2017 Dec 11;13(12):e1006762. doi: 10.1371/journal.ppat.1006762. eCollection 2017 Dec.

4.

Changes in the lung bacteriome in relation to antipseudomonal therapy in children with cystic fibrosis.

Kramná L, Dřevínek P, Lin J, Kulich M, Cinek O.

Folia Microbiol (Praha). 2018 Mar;63(2):237-248. doi: 10.1007/s12223-017-0562-3. Epub 2017 Nov 10.

PMID:
29127619
5.

Increasing incidence of Clostridium difficile ribotype 001 associated with severe course of the infection and previous fluoroquinolone use in the Czech Republic, 2015.

Krutova M, Matejkova J, Drevinek P, Kuijper EJ, Nyc O; study group.

Eur J Clin Microbiol Infect Dis. 2017 Nov;36(11):2251-2258. doi: 10.1007/s10096-017-3055-z. Epub 2017 Jul 5.

PMID:
28681203
6.

Burkholderia cepacia complex in cystic fibrosis in the post-epidemic period: multilocus sequence typing-based approach.

Fila L, Dřevínek P.

Folia Microbiol (Praha). 2017 Nov;62(6):509-514. doi: 10.1007/s12223-017-0523-x. Epub 2017 Mar 31.

PMID:
28364392
7.

Sequential Burkholderia cenocepacia Isolates from Siblings with Cystic Fibrosis Show Increased Lung Cell Attachment.

Cullen L, O'Connor A, Drevinek P, Schaffer K, McClean S.

Am J Respir Crit Care Med. 2017 Mar 15;195(6):832-835. doi: 10.1164/rccm.201607-1360LE. No abstract available.

PMID:
28294652
8.

Acetic acid is elevated in the exhaled breath of cystic fibrosis patients.

Španěl P, Sovová K, Dryahina K, Doušová T, Dřevínek P, Smith D.

J Cyst Fibros. 2017 Sep;16(5):e17-e18. doi: 10.1016/j.jcf.2017.02.001. Epub 2017 Feb 16. No abstract available.

PMID:
28215621
9.

A case report of a cochlear implant infection - A reason to explant the device?

Skrivan J, Drevinek P.

Cochlear Implants Int. 2016 Sep;17(5):246-249. Epub 2016 Sep 9.

PMID:
27609547
10.

Do linear logistic model analyses of volatile biomarkers in exhaled breath of cystic fibrosis patients reliably indicate Pseudomonas aeruginosa infection?

Španěl P, Sovová K, Dryahina K, Doušová T, Dřevínek P, Smith D.

J Breath Res. 2016 Aug 17;10(3):036013. doi: 10.1088/1752-7155/10/3/036013.

PMID:
27532768
11.

Understanding the Pathogenicity of Burkholderia contaminans, an Emerging Pathogen in Cystic Fibrosis.

Nunvar J, Kalferstova L, Bloodworth RA, Kolar M, Degrossi J, Lubovich S, Cardona ST, Drevinek P.

PLoS One. 2016 Aug 11;11(8):e0160975. doi: 10.1371/journal.pone.0160975. eCollection 2016.

12.

Clostridium difficile PCR ribotypes 001 and 176 - the common denominator of C. difficile infection epidemiology in the Czech Republic, 2014.

Krutova M, Matejkova J, Kuijper EJ, Drevinek P, Nyc O; Czech Clostridium difficile study group.

Euro Surveill. 2016 Jul 21;21(29). doi: 10.2807/1560-7917.ES.2016.21.29.30296.

13.

Ivacaftor in cystic fibrosis adults: Czech experience with six years of follow-up.

Fila L, Valentova Bartakova L, Grandcourtova A, Marel M, Drnek R, Bilkova A, Macek M, Drevinek P.

Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2016 Jun;160(2):276-9. doi: 10.5507/bp.2016.029. Epub 2016 May 25.

14.

Breath concentration of acetic acid vapour is elevated in patients with cystic fibrosis.

Smith D, Sovová K, Dryahina K, Doušová T, Dřevínek P, Španěl P.

J Breath Res. 2016 May 17;10(2):021002. doi: 10.1088/1752-7155/10/2/021002.

PMID:
27184114
15.

Cost-of-illness analysis and regression modeling in cystic fibrosis: a retrospective prevalence-based study.

Mlčoch T, Klimeš J, Fila L, Vávrová V, Skalická V, Turnovec M, Krulišová V, Jirčíková J, Zemková D, Dědečková KV, Bílková A, Frühaufová V, Homola L, Friedmannová Z, Drnek R, Dřevínek P, Doležal T, Macek M Jr.

Eur J Health Econ. 2017 Jan;18(1):73-82. doi: 10.1007/s10198-015-0759-9. Epub 2016 Jan 7.

PMID:
26743971
16.

How and why to monitor Pseudomonas aeruginosa infections in the long term at a cystic fibrosis centre.

Kalferstova L, Vilimovska Dedeckova K, Antuskova M, Melter O, Drevinek P.

J Hosp Infect. 2016 Jan;92(1):54-60. doi: 10.1016/j.jhin.2015.09.010. Epub 2015 Oct 8.

PMID:
26597636
17.

Report of the European Respiratory Society/European Cystic Fibrosis Society task force on the care of adults with cystic fibrosis.

Elborn JS, Bell SC, Madge SL, Burgel PR, Castellani C, Conway S, De Rijcke K, Dembski B, Drevinek P, Heijerman HG, Innes JA, Lindblad A, Marshall B, Olesen HV, Reimann AL, Solé A, Viviani L, Wagner TO, Welte T, Blasi F.

Eur Respir J. 2016 Feb;47(2):420-8. doi: 10.1183/13993003.00592-2015. Epub 2015 Oct 9.

18.

Identification of bacteria from aerobic and anaerobic blood cultures after short cultivation by matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry.

Nunvar J, Drevinek P.

J Med Microbiol. 2015 Oct;64(10):1253-5. doi: 10.1099/jmm.0.000140. Epub 2015 Jul 17. No abstract available.

PMID:
26297327
19.

Phenotypic characterization of an international Pseudomonas aeruginosa reference panel: strains of cystic fibrosis (CF) origin show less in vivo virulence than non-CF strains.

Cullen L, Weiser R, Olszak T, Maldonado RF, Moreira AS, Slachmuylders L, Brackman G, Paunova-Krasteva TS, Zarnowiec P, Czerwonka G, Reilly J, Drevinek P, Kaca W, Melter O, De Soyza A, Perry A, Winstanley C, Stoitsova SR, Lavigne R, Mahenthiralingam E, Sá-Correia I, Coenye T, Drulis-Kawa Z, Augustyniak D, Valvano MA, McClean S.

Microbiology. 2015 Oct;161(10):1961-77. doi: 10.1099/mic.0.000155. Epub 2015 Aug 6.

PMID:
26253522
20.

Draft Genome Sequences of Burkholderia contaminans, a Burkholderia cepacia Complex Species That Is Increasingly Recovered from Cystic Fibrosis Patients.

Bloodworth RA, Selin C, López De Volder MA, Drevinek P, Galanternik L, Degrossi J, Cardona ST.

Genome Announc. 2015 Aug 6;3(4). pii: e00766-15. doi: 10.1128/genomeA.00766-15.

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