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Year Number of Results
2009 1
2015 2
2016 2
2017 2
2018 1
2019 2
2020 1
2021 2
2022 1
2023 1
2024 0

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13 results

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Page 1
Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR.
Wainwright CE, Elborn JS, Ramsey BW, Marigowda G, Huang X, Cipolli M, Colombo C, Davies JC, De Boeck K, Flume PA, Konstan MW, McColley SA, McCoy K, McKone EF, Munck A, Ratjen F, Rowe SM, Waltz D, Boyle MP; TRAFFIC Study Group; TRANSPORT Study Group. Wainwright CE, et al. N Engl J Med. 2015 Jul 16;373(3):220-31. doi: 10.1056/NEJMoa1409547. Epub 2015 May 17. N Engl J Med. 2015. PMID: 25981758 Free PMC article. Clinical Trial.
The effect of nintedanib on lung functions and survival in idiopathic pulmonary fibrosis: real-life analysis of the Czech EMPIRE registry.
Štefániková M, Doubková M, Ovesná P, Šterclová M, Lacina L, Žurková M, Plačková M, Bartoš V, Janíčková I, Bittenglová R, Anton J, Sýkorová Ľ, Lošťáková V, Musilová P, Šuldová H, Mokošová R, Didyk J, Šišáková L, Lisá P, Lněnička J, Dařičková H, Doležel D, Pšikalová J, Tyl R, Králová R, Vašáková MK. Štefániková M, et al. Among authors: bittenglova r. BMC Pulm Med. 2023 May 3;23(1):154. doi: 10.1186/s12890-023-02450-3. BMC Pulm Med. 2023. PMID: 37138274 Free PMC article.
[Diagnostics of cystic fibrosis in adults].
Fila L, Grandcourtová A, Bartáková LV, Antušová Z, Pokojová E, Herout V, Jakubec P, Bittenglová R, Marel M. Fila L, et al. Among authors: bittenglova r. Vnitr Lek. 2016 Spring;62(5):360-4. Vnitr Lek. 2016. PMID: 27319228 Czech.
DSP rs2076295 variants influence nintedanib and pirfenidone outcomes in idiopathic pulmonary fibrosis: a pilot study.
Doubkova M, Kriegova E, Littnerova S, Schneiderova P, Sterclova M, Bartos V, Plackova M, Zurkova M, Bittenglova R, Lostaková V, Siskova L, Lisa P, Suldova H, Doubek M, Psikalova J, Snizek T, Musilova P, Vasakova M. Doubkova M, et al. Among authors: bittenglova r. Ther Adv Respir Dis. 2021 Jan-Dec;15:17534666211042529. doi: 10.1177/17534666211042529. Ther Adv Respir Dis. 2021. PMID: 34515605 Free PMC article.
The European MultiPartner IPF registry (EMPIRE): validating long-term prognostic factors in idiopathic pulmonary fibrosis.
Tran T, Šterclová M, Mogulkoc N, Lewandowska K, Müller V, Hájková M, Kramer MR, Jovanović D, Tekavec-Trkanjec J, Studnicka M, Stoeva N, Hejduk K, Dušek L, Suissa S, Vašáková M; EMPIRE registry. Tran T, et al. Respir Res. 2020 Jan 8;21(1):11. doi: 10.1186/s12931-019-1271-z. Respir Res. 2020. PMID: 31915023 Free PMC article.
Biomarkers of extracellular matrix turnover in patients with idiopathic pulmonary fibrosis given nintedanib (INMARK study): a randomised, placebo-controlled study.
Maher TM, Stowasser S, Nishioka Y, White ES, Cottin V, Noth I, Selman M, Rohr KB, Michael A, Ittrich C, Diefenbach C, Jenkins RG; INMARK trial investigators. Maher TM, et al. Lancet Respir Med. 2019 Sep;7(9):771-779. doi: 10.1016/S2213-2600(19)30255-3. Epub 2019 Jul 17. Lancet Respir Med. 2019. PMID: 31326319 Free article. Clinical Trial.
[Idiopathic pulmonary fibrosis prognostic factors - analysis of the Czech registry].
Doubková M, Uher M, Bartoš V, Šterclová M, Lacina L, Lošťáková V, Binková I, Plačková M, Žurková M, Bittenglová R, Pšikalová J, Šišková L, Lisá P, Petřík F, Polák J, Řihák V, Skřičková J, Vašáková M. Doubková M, et al. Among authors: bittenglova r. Cas Lek Cesk. 2016;155(4):22-8. Cas Lek Cesk. 2016. PMID: 27481198 Czech.
13 results