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Items: 1 to 20 of 22

1.

Continued Smoking in Lung Transplant Patients: A Cross Sectional Survey.

Zmeškal M, Králíková E, Kurcová I, Pafko P, Lischke R, Fila L, Valentová Bartáková L, Fraser K.

Zdr Varst. 2015 Dec 16;55(1):29-35. doi: 10.1515/sjph-2016-0005. eCollection 2016 Mar.

2.

[The differential diagnosis of pleural effusions].

Marel M, Fila L, Červená M.

Vnitr Lek. 2016 Fall;62(7-8):598-604. Czech.

PMID:
27627084
3.

[Diagnostics of cystic fibrosis in adults].

Fila L, Grandcourtová A, Bartáková LV, Antušová Z, Pokojová E, Herout V, Jakubec P, Bittenglová R, Marel M.

Vnitr Lek. 2016 Spring;62(5):360-4. Czech.

PMID:
27319228
4.

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.

5.

Human Epididymis Protein 4: A Novel Serum Inflammatory Biomarker in Cystic Fibrosis.

Nagy B Jr, Nagy B, Fila L, Clarke LA, Gönczy F, Bede O, Nagy D, Újhelyi R, Szabó Á, Anghelyi A, Major M, Bene Z, Fejes Z, Antal-Szalmás P, Bhattoa HP, Balla G, Kappelmayer J, Amaral MD, Macek M Jr, Balogh I.

Chest. 2016 Sep;150(3):661-72. doi: 10.1016/j.chest.2016.04.006. Epub 2016 Apr 19.

PMID:
27105680
6.

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. 2016 Jan 7. [Epub ahead of print]

PMID:
26743971
7.

Lung cancer, pulmonary emphysema and pleural effusion: An autopsy study.

Marel M, Koubkova L, Kovarikova Z, Grandcourtova A, Petrik F, Hroudova H, Capkova L, Kodet R, Fila L.

Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2015 Dec;159(4):642-7. doi: 10.5507/bp.2015.024. Epub 2015 May 19.

8.

Characterization of Staphylococcus aureus Strains Isolated from Czech Cystic Fibrosis Patients: High Rate of Ribosomal Mutation Conferring Resistance to MLS(B) Antibiotics as a Result of Long-Term and Low-Dose Azithromycin Treatment.

Tkadlec J, Vařeková E, Pantůček R, Doškař J, Růžičková V, Botka T, Fila L, Melter O.

Microb Drug Resist. 2015 Aug;21(4):416-23. doi: 10.1089/mdr.2014.0276. Epub 2015 Mar 31.

PMID:
25826283
9.

Gene expression profiling of Burkholderia cenocepacia at the time of cepacia syndrome: loss of motility as a marker of poor prognosis?

Kalferstova L, Kolar M, Fila L, Vavrova J, Drevinek P.

J Clin Microbiol. 2015 May;53(5):1515-22. doi: 10.1128/JCM.03605-14. Epub 2015 Feb 18.

10.

Oxidative stress in cystic fibrosis patients with Burkholderia cenocepacia airway colonization: relation of 8-isoprostane concentration in exhaled breath condensate to lung function decline.

Fila L, Grandcourtová A, Chládek J, Musil J.

Folia Microbiol (Praha). 2014 May;59(3):217-22. doi: 10.1007/s12223-013-0285-z. Epub 2013 Oct 17.

PMID:
24132725
11.

Nitrites and nitrates in exhaled breath condensate in cystic fibrosis: relation to clinical parameters.

Fila L, Chladek J, Maly M, Musil J.

Bratisl Lek Listy. 2013;114(9):503-7.

PMID:
24020705
12.

Systemic soluble receptor for advanced glycation endproducts is a biomarker of emphysema and associated with AGER genetic variants in patients with chronic obstructive pulmonary disease.

Cheng DT, Kim DK, Cockayne DA, Belousov A, Bitter H, Cho MH, Duvoix A, Edwards LD, Lomas DA, Miller BE, Reynaert N, Tal-Singer R, Wouters EF, Agustí A, Fabbri LM, Rames A, Visvanathan S, Rennard SI, Jones P, Parmar H, MacNee W, Wolff G, Silverman EK, Mayer RJ, Pillai SG; TESRA and ECLIPSE Investigators.

Am J Respir Crit Care Med. 2013 Oct 15;188(8):948-57. doi: 10.1164/rccm.201302-0247OC.

PMID:
23947473
13.

Distribution of CFTR mutations in the Czech population: positive impact of integrated clinical and laboratory expertise, detection of novel/de novo alleles and relevance for related/derived populations.

Křenková P, Piskáčková T, Holubová A, Balaščaková M, Krulišová V, Čamajová J, Turnovec M, Libik M, Norambuena P, Štambergová A, Dvořáková L, Skalická V, Bartošová J, Kučerová T, Fila L, Zemková D, Vávrová V, Koudová M, Macek M, Krebsová A, Macek M Jr.

J Cyst Fibros. 2013 Sep;12(5):532-7. doi: 10.1016/j.jcf.2012.12.002. Epub 2012 Dec 29.

14.

PCR detection of Burkholderia cepacia complex as one of key factors to handle a long-term outbreak.

Dedeckova K, Fila L, Skalicka V, Bartosova J, Kucerova T, Vavrova V, Zemkova D, Kalferstova L, Melter O, Cinek O, Drevinek P.

J Cyst Fibros. 2012 Sep;11(5):440-5. doi: 10.1016/j.jcf.2012.04.005. Epub 2012 May 22.

15.

Impairment of nasal mucociliary clearance in former smokers with stable chronic obstructive pulmonary disease relates to the presence of a chronic bronchitis phenotype.

Koblizek V, Tomsova M, Cermakova E, Papousek P, Pracharova S, Mandalia RA, Ceral J, Novosad J, Fila L, Sedlak V, Ruta J, Bartos V, Salajka F, Hrnciarik M.

Rhinology. 2011 Oct;49(4):397-406. doi: 10.4193/Rhino11.051.

PMID:
21991564
16.

Lung transplantation in cystic fibrosis patients in the Czech Republic: initial single-center experience.

Bartáková LV, Fila L, Adámek S, Pozniak J, Malý M, Burkert J, Šimonek J, Lischke R.

Transplant Proc. 2010 Nov;42(9):3711-3. doi: 10.1016/j.transproceed.2010.09.007.

PMID:
21094844
17.

[Examination of exhaled breath condensate in cystic fibrosis].

Fila L, Musil J.

Cas Lek Cesk. 2010;149(4):173-7. Review. Czech.

PMID:
20518250
18.

Genetic modifiers of liver disease in cystic fibrosis.

Bartlett JR, Friedman KJ, Ling SC, Pace RG, Bell SC, Bourke B, Castaldo G, Castellani C, Cipolli M, Colombo C, Colombo JL, Debray D, Fernandez A, Lacaille F, Macek M Jr, Rowland M, Salvatore F, Taylor CJ, Wainwright C, Wilschanski M, Zemková D, Hannah WB, Phillips MJ, Corey M, Zielenski J, Dorfman R, Wang Y, Zou F, Silverman LM, Drumm ML, Wright FA, Lange EM, Durie PR, Knowles MR; Gene Modifier Study Group.

JAMA. 2009 Sep 9;302(10):1076-83. doi: 10.1001/jama.2009.1295.

19.

[Twenty years of care for cystic fibrosis adults in Czech Republic].

Fila L, Sedlák V, Binková I, Jakubec P, Bittenglová R, Musil J.

Vnitr Lek. 2009 Jun;55(6):542-8. Czech.

PMID:
19662884
20.

Detection of two Alu insertions in the CFTR gene.

Chen JM, Masson E, Macek M Jr, Raguénès O, Piskackova T, Fercot B, Fila L, Cooper DN, Audrézet MP, Férec C.

J Cyst Fibros. 2008 Jan;7(1):37-43. Epub 2007 May 24.

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