Tümmler B - Search Results

1

Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on Lung Clearance Index and Magnetic Resonance Imaging in Patients with Cystic Fibrosis and One or Two F508del Alleles.

Graeber SY, Renz DM, Stahl M, Pallenberg ST, Sommerburg O, Naehrlich L, Berges J, Dohna M, Ringshausen FC, Doellinger F, Vitzthum C, Röhmel J, Allomba C, Hämmerling S, Barth S, Rückes-Nilges C, Wielpütz MO, Hansen G, Vogel-Claussen J, Tümmler B, Mall MA, Dittrich AM. Graeber SY, et al. Among authors: tummler b. Am J Respir Crit Care Med. 2022 Aug 1;206(3):311-320. doi: 10.1164/rccm.202201-0219OC. Am J Respir Crit Care Med. 2022. PMID: 35536314

2

Expression levels of FAS are regulated through an evolutionary conserved element in intron 2, which modulates cystic fibrosis disease severity.

Kumar V, Becker T, Jansen S, van Barneveld A, Boztug K, Wölfl S, Tümmler B, Stanke F. Kumar V, et al. Among authors: tummler b. Genes Immun. 2008 Dec;9(8):689-96. doi: 10.1038/gene.2008.63. Epub 2008 Aug 7. Genes Immun. 2008. PMID: 18685642

3

Concordant genotype of upper and lower airways P aeruginosa and S aureus isolates in cystic fibrosis.

Mainz JG, Naehrlich L, Schien M, Käding M, Schiller I, Mayr S, Schneider G, Wiedemann B, Wiehlmann L, Cramer N, Pfister W, Kahl BC, Beck JF, Tümmler B. Mainz JG, et al. Among authors: tummler b. Thorax. 2009 Jun;64(6):535-40. doi: 10.1136/thx.2008.104711. Epub 2009 Mar 11. Thorax. 2009. PMID: 19282318

4

Pseudomonas aeruginosa microevolution during cystic fibrosis lung infection establishes clones with adapted virulence.

Bragonzi A, Paroni M, Nonis A, Cramer N, Montanari S, Rejman J, Di Serio C, Döring G, Tümmler B. Bragonzi A, et al. Among authors: tummler b. Am J Respir Crit Care Med. 2009 Jul 15;180(2):138-45. doi: 10.1164/rccm.200812-1943OC. Epub 2009 May 7. Am J Respir Crit Care Med. 2009. PMID: 19423715

5

Intestinal current measurement for diagnostic classification of patients with questionable cystic fibrosis: validation and reference data.

Derichs N, Sanz J, Von Kanel T, Stolpe C, Zapf A, Tümmler B, Gallati S, Ballmann M. Derichs N, et al. Among authors: tummler b. Thorax. 2010 Jul;65(7):594-9. doi: 10.1136/thx.2009.125088. Thorax. 2010. PMID: 20627915

6

Acute intratracheal Pseudomonas aeruginosa infection in cystic fibrosis mice is age-independent.

Munder A, Wölbeling F, Kerber-Momot T, Wedekind D, Baumann U, Gulbins E, Tümmler B. Munder A, et al. Among authors: tummler b. Respir Res. 2011 Nov 7;12(1):148. doi: 10.1186/1465-9921-12-148. Respir Res. 2011. PMID: 22059807 Free PMC article.

7

Nasal potential difference measurements in diagnosis of cystic fibrosis: an international survey.

Naehrlich L, Ballmann M, Davies J, Derichs N, Gonska T, Hjelte L, van Konigsbruggen-Rietschel S, Leal T, Melotti P, Middleton P, Tümmler B, Vermeulen F, Wilschanski M; ECFS Diagnostic Network Working Group. Naehrlich L, et al. Among authors: tummler b. J Cyst Fibros. 2014 Jan;13(1):24-8. doi: 10.1016/j.jcf.2013.08.006. Epub 2013 Sep 7. J Cyst Fibros. 2014. PMID: 24022019 Free article.

8

Mutation-specific therapy in cystic fibrosis: the earlier, the better.

Tümmler B. Tümmler B. Lancet Respir Med. 2013 Oct;1(8):591-592. doi: 10.1016/S2213-2600(13)70186-3. Epub 2013 Sep 10. Lancet Respir Med. 2013. PMID: 24461654 No abstract available.

9

The stony road to phe508del CFTR pharmacotherapy: smoothing the first rock.

Tümmler B. Tümmler B. Lancet Respir Med. 2014 Jul;2(7):508-9. doi: 10.1016/S2213-2600(14)70136-5. Epub 2014 Jun 24. Lancet Respir Med. 2014. PMID: 24973279 No abstract available.

10

Current concepts: host-pathogen interactions in cystic fibrosis airways disease.

Tang AC, Turvey SE, Alves MP, Regamey N, Tümmler B, Hartl D. Tang AC, et al. Among authors: tummler b. Eur Respir Rev. 2014 Sep;23(133):320-32. doi: 10.1183/09059180.00006113. Eur Respir Rev. 2014. PMID: 25176968 Free PMC article. Review.

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