Sabine Renner
Overview
Explore the profile of Sabine Renner including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
163
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Recent Articles
1.
Rumpf C, Janssen T, Hait R, Romme K, Decker C, Peters J, et al.
Am J Respir Crit Care Med
. 2025 Feb;
PMID: 39918841
Rationale: The mucoid phenotype of is caused by adaptation. Excessive biofilm formation associated with a protective effect for mucoid was observed in isolates from respiratory samples of people with cystic...
2.
Sieber J, Renner S, Lakatos-Krepcik A, Szepfalusi Z
Front Pediatr
. 2021 Apr;
9:663228.
PMID: 33869120
Drug desensitization can be achieved successfully by gradual drug dose increases in different protocols. Most protocols are designed to obtain temporal tolerance. The data on long-term maintenance of drug tolerance...
3.
Zeyda M, Schanzer A, Basek P, Bauer V, Eber E, Ellemunter H, et al.
Diagnostics (Basel)
. 2021 Mar;
11(2).
PMID: 33668470
In Austria, newborns have been screened for cystic fibrosis (CF) by analyzing immunoreactive trypsinogen (IRT) from dried blood spots (DBS)s for nearly 20 years. Recently, pancreatitis-associated protein (PAP) analysis was...
4.
Renner S, Nachbaur E, Jaksch P, Dehlink E
J Fungi (Basel)
. 2020 Dec;
6(4).
PMID: 33371198
Cystic fibrosis is the most common autosomal-recessive metabolic disease in the Western world. Impaired trans-membrane chloride transport via the cystic fibrosis transmembrane conductance regulator (CFTR) protein causes thickened body fluids....
5.
Farrell P, Ferec C, Macek M, Frischer T, Renner S, Riss K, et al.
Eur J Hum Genet
. 2018 Aug;
26(12):1832-1839.
PMID: 30089827
The high incidence of cystic fibrosis (CF) is due to the frequency of the c.1521_1523delCTT variant in the cystic fibrosis transmembrane conductance regulator (CFTR), but its age and origin are...
6.
Gona-Hopler M, Pfaller B, Argeny J, Kanolzer S, Gruber S, Schmidthaler K, et al.
ERJ Open Res
. 2017 Nov;
3(4).
PMID: 29164145
http://ow.ly/XXwv30furqs.
7.
Diesner S, Lukas J, Stifter E, Raimann A, Nachbaur E, Eiwegger T, et al.
Klin Padiatr
. 2017 Apr;
229(2):96-99.
PMID: 28444655
No abstract available.
8.
Zacharasiewicz A, Renner S, Haderer F, Weber M, Dehlink E, Szepfalusi Z, et al.
Wien Klin Wochenschr
. 2017 Mar;
129(15-16):533-539.
PMID: 28281010
Values: Zapletal 86.6% (SD 20.6), GLI 79.9% (SD 20.3) and 32% (n = 497/1543) were misclassified as normal when using Zapletal. Despite showing no overall differences in FEV1 and forced...
9.
Frischer T, Eber E, Ellemunter H, Zacharasiewicz A, Kaluza I, Riedler J, et al.
Wien Klin Wochenschr
. 2017 Feb;
129(15-16):527-532.
PMID: 28236043
Registry data for patients with cystic fibrosis (CF) are increasingly used to evaluate the natural history, for benchmarking of therapy and in order to identify eligible patients for clinical studies....
10.
Lex C, Korten I, Hofmann A, Renner S, Szepfalusi Z, Frischer T, et al.
Wien Med Wochenschr
. 2015 Sep;
165(17-18):361-5.
PMID: 26376983
Background: The new lung function reference values of the global lung initiative (GLI) are recommended by most health societies. The aim of this study was to analyze FEV1- and FEV1/FVC-values...