Hector A - Search Results

1

Inhalation treatment with glutathione in patients with cystic fibrosis. A randomized clinical trial.

Griese M, Kappler M, Eismann C, Ballmann M, Junge S, Rietschel E, van Koningsbruggen-Rietschel S, Staab D, Rolinck-Werninghaus C, Mellies U, Köhnlein T, Wagner T, König S, Teschler H, Heuer HE, Kopp M, Heyder S, Hammermann J, Küster P, Honer M, Mansmann U, Beck-Speier I, Hartl D, Fuchs C; Glutathione Study Group; Hector A. Griese M, et al. Among authors: hector a. Am J Respir Crit Care Med. 2013 Jul 1;188(1):83-9. doi: 10.1164/rccm.201303-0427OC. Am J Respir Crit Care Med. 2013. PMID: 23631796 Clinical Trial.

2

In vitro inhibition of neutrophil elastase activity by inhaled anti-Pseudomonas antibiotics used in cystic fibrosis patients.

Hector A, Kappler M, Griese M. Hector A, et al. Mediators Inflamm. 2010;2010:809591. doi: 10.1155/2010/809591. Epub 2010 Jun 16. Mediators Inflamm. 2010. PMID: 20634941 Free PMC article.

3

Reply: glutathione inhalation treatments in cystic fibrosis: the interference of airway γ-glutamyltransferase.

Hector A, Griese M. Hector A, et al. Am J Respir Crit Care Med. 2014 Jan 15;189(2):234-5. doi: 10.1164/rccm.201307-1289LE. Am J Respir Crit Care Med. 2014. PMID: 24428658 No abstract available.

4

Oxidative stress in cystic fibrosis lung disease: an early event, but worth targeting?

Hector A, Griese M, Hartl D. Hector A, et al. Eur Respir J. 2014 Jul;44(1):17-9. doi: 10.1183/09031936.00038114. Eur Respir J. 2014. PMID: 24982050 Free article. No abstract available.

5

Increasing sputum levels of gamma-glutamyltransferase may identify cystic fibrosis patients who do not benefit from inhaled glutathione.

Corti A, Griese M, Hector A, Pompella A. Corti A, et al. Among authors: hector a. J Cyst Fibros. 2017 May;16(3):342-345. doi: 10.1016/j.jcf.2016.12.002. Epub 2016 Dec 14. J Cyst Fibros. 2017. PMID: 27988297 Free article. Clinical Trial.

6

Novel method to process cystic fibrosis sputum for determination of oxidative state.

Hector A, Jonas F, Kappler M, Feilcke M, Hartl D, Griese M. Hector A, et al. Respiration. 2010;80(5):393-400. doi: 10.1159/000271607. Epub 2009 Dec 23. Respiration. 2010. PMID: 20029169 Free article.

7

Ursodeoxycholic acid therapy in cystic fibrosis liver disease--a retrospective long-term follow-up case-control study.

Kappler M, Espach C, Schweiger-Kabesch A, Lang T, Hartl D, Hector A, Glasmacher C, Griese M. Kappler M, et al. Among authors: hector a. Aliment Pharmacol Ther. 2012 Aug;36(3):266-73. doi: 10.1111/j.1365-2036.2012.05177.x. Epub 2012 Jun 7. Aliment Pharmacol Ther. 2012. PMID: 22670841 Free article.

8

CXCR1 and CXCR2 haplotypes synergistically modulate cystic fibrosis lung disease.

Kormann MS, Hector A, Marcos V, Mays LE, Kappler M, Illig T, Klopp N, Zeilinger S, Carevic M, Rieber N, Eickmeier O, Zielen S, Gaggar A, Moepps B, Griese M, Hartl D. Kormann MS, et al. Among authors: hector a. Eur Respir J. 2012 Jun;39(6):1385-90. doi: 10.1183/09031936.00130011. Epub 2011 Nov 16. Eur Respir J. 2012. PMID: 22088968 Free article.

9

Expression and regulation of interferon-related development regulator-1 in cystic fibrosis neutrophils.

Hector A, Kormann M, Kammermeier J, Burdi S, Marcos V, Rieber N, Mays L, Illig T, Klopp N, Falkenstein F, Kappler M, Riethmueller J, Graepler-Mainka U, Stern M, Eickmeier O, Serve F, Zielen S, Döring G, Griese M, Hartl D. Hector A, et al. Am J Respir Cell Mol Biol. 2013 Jan;48(1):71-7. doi: 10.1165/rcmb.2012-0061OC. Epub 2012 Oct 4. Am J Respir Cell Mol Biol. 2013. PMID: 23043087

10

The chemokine CCL18 characterises Pseudomonas infections in cystic fibrosis lung disease.

Hector A, Kröner C, Carevic M, Bakele M, Rieber N, Riethmüller J, Griese M, Zissel G, Hartl D. Hector A, et al. Eur Respir J. 2014 Dec;44(6):1608-15. doi: 10.1183/09031936.00070014. Epub 2014 Aug 19. Eur Respir J. 2014. PMID: 25142483 Free article.

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