Ellemunter H - Search Results

1

Tezacaftor/ivacaftor in people with cystic fibrosis heterozygous for minimal function CFTR mutations.

Munck A, Kerem E, Ellemunter H, Campbell D, Wang LT, Ahluwalia N, Owen CA, Wainwright C. Munck A, et al. Among authors: ellemunter h. J Cyst Fibros. 2020 Nov;19(6):962-968. doi: 10.1016/j.jcf.2020.04.015. Epub 2020 Jun 13. J Cyst Fibros. 2020. PMID: 32546431 Free article. Clinical Trial.

2

Guidelines for the diagnosis and management of distal intestinal obstruction syndrome in cystic fibrosis patients.

Colombo C, Ellemunter H, Houwen R, Munck A, Taylor C, Wilschanski M; ECFS. Colombo C, et al. Among authors: ellemunter h. J Cyst Fibros. 2011 Jun;10 Suppl 2:S24-8. doi: 10.1016/S1569-1993(11)60005-2. J Cyst Fibros. 2011. PMID: 21658638 Free article. Review.

3

Reference percentiles for FEV(1) and BMI in European children and adults with cystic fibrosis.

Boëlle PY, Viviani L, Busson PF, Olesen HV, Ravilly S, Stern M, Assael BM, Barreto C, Drevinek P, Thomas M, Krivec U, Mei-Zahav M, Vibert JF, Clement A, Mehta A, Corvol H; French CF Modifier Gene Study Investigators; European CF Registry Working Group. Boëlle PY, et al. Orphanet J Rare Dis. 2012 Sep 7;7:64. doi: 10.1186/1750-1172-7-64. Orphanet J Rare Dis. 2012. PMID: 22958330 Free PMC article.

4

Factors associated with FEV1 decline in cystic fibrosis: analysis of the ECFS patient registry.

Kerem E, Viviani L, Zolin A, MacNeill S, Hatziagorou E, Ellemunter H, Drevinek P, Gulmans V, Krivec U, Olesen H; ECFS Patient Registry Steering Group. Kerem E, et al. Among authors: ellemunter h. Eur Respir J. 2014 Jan;43(1):125-33. doi: 10.1183/09031936.00166412. Epub 2013 Apr 18. Eur Respir J. 2014. PMID: 23598952 Free article.

5

Different approaches to evaluate patient experience and satisfaction in CF centres.

Steinkamp G, Ellemunter H, Schwarz C, Stahl K. Steinkamp G, et al. Among authors: ellemunter h. J Cyst Fibros. 2015 Sep;14(5):E19-20. doi: 10.1016/j.jcf.2015.05.010. Epub 2015 Jun 10. J Cyst Fibros. 2015. PMID: 26071056 Free article. No abstract available.

6

Long-term improvement of lung clearance index in patients with mild cystic fibrosis lung disease: Does hypertonic saline play a role?

Ellemunter H, Eder J, Fuchs S, Gappa M, Steinkamp G. Ellemunter H, et al. J Cyst Fibros. 2016 Jan;15(1):123-6. doi: 10.1016/j.jcf.2015.06.009. Epub 2015 Jul 17. J Cyst Fibros. 2016. PMID: 26190829 Free article.

7

Psychological resilience and intolerance of uncertainty in coping with cystic fibrosis.

Mitmansgruber H, Smrekar U, Rabanser B, Beck T, Eder J, Ellemunter H. Mitmansgruber H, et al. Among authors: ellemunter h. J Cyst Fibros. 2016 Sep;15(5):689-95. doi: 10.1016/j.jcf.2015.11.011. Epub 2015 Dec 10. J Cyst Fibros. 2016. PMID: 26686827 Free article.

8

Low sodium status in cystic fibrosis-as assessed by calculating fractional Na(+) excretion-is associated with decreased growth parameters.

Knepper C, Ellemunter H, Eder J, Niedermayr K, Haerter B, Hofer P, Scholl-Bürgi S, Müller T, Heinz-Erian P. Knepper C, et al. Among authors: ellemunter h. J Cyst Fibros. 2016 May;15(3):400-5. doi: 10.1016/j.jcf.2015.12.010. Epub 2016 Jan 6. J Cyst Fibros. 2016. PMID: 26777601 Free article.

9

International prospective study of distal intestinal obstruction syndrome in cystic fibrosis: Associated factors and outcome.

Munck A, Alberti C, Colombo C, Kashirskaya N, Ellemunter H, Fotoulaki M, Houwen R, Robberecht E, Boizeau P, Wilschanski M; CF/Pancreas ESPGHAN Working Group and DIOS Study Group. Munck A, et al. Among authors: ellemunter h. J Cyst Fibros. 2016 Jul;15(4):531-9. doi: 10.1016/j.jcf.2016.02.002. Epub 2016 Feb 23. J Cyst Fibros. 2016. PMID: 26927601 Free article.

10

Cystic fibrosis in Austria.

Frischer T, Eber E, Ellemunter H, Zacharasiewicz A, Kaluza I, Riedler J, Renner S. Frischer T, et al. Among authors: ellemunter h. Wien Klin Wochenschr. 2017 Aug;129(15-16):527-532. doi: 10.1007/s00508-017-1179-x. Epub 2017 Feb 24. Wien Klin Wochenschr. 2017. PMID: 28236043

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