Mainz JG - Search Results

1

Adherence to therapies in cystic fibrosis: a targeted literature review.

Narayanan S, Mainz JG, Gala S, Tabori H, Grossoehme D. Narayanan S, et al. Among authors: mainz jg. Expert Rev Respir Med. 2017 Feb;11(2):129-145. doi: 10.1080/17476348.2017.1280399. Epub 2017 Jan 20. Expert Rev Respir Med. 2017. PMID: 28107795 Review.

2

Smell in cystic fibrosis.

Lindig J, Steger C, Beiersdorf N, Michl R, Beck JF, Hummel T, Mainz JG. Lindig J, et al. Among authors: mainz jg. Eur Arch Otorhinolaryngol. 2013 Mar;270(3):915-21. doi: 10.1007/s00405-012-2124-2. Epub 2012 Aug 14. Eur Arch Otorhinolaryngol. 2013. PMID: 22890694

3

Aspects of pulmonary drug delivery strategies for infections in cystic fibrosis--where do we stand?

Klinger-Strobel M, Lautenschläger C, Fischer D, Mainz JG, Bruns T, Tuchscherr L, Pletz MW, Makarewicz O. Klinger-Strobel M, et al. Among authors: mainz jg. Expert Opin Drug Deliv. 2015 Aug;12(8):1351-74. doi: 10.1517/17425247.2015.1007949. Epub 2015 Feb 2. Expert Opin Drug Deliv. 2015. PMID: 25642831 Review.

4

Intestinal Current Measurements Detect Activation of Mutant CFTR in Patients with Cystic Fibrosis with the G551D Mutation Treated with Ivacaftor.

Graeber SY, Hug MJ, Sommerburg O, Hirtz S, Hentschel J, Heinzmann A, Dopfer C, Schulz A, Mainz JG, Tümmler B, Mall MA. Graeber SY, et al. Among authors: mainz jg. Am J Respir Crit Care Med. 2015 Nov 15;192(10):1252-5. doi: 10.1164/rccm.201507-1271LE. Am J Respir Crit Care Med. 2015. PMID: 26568242 No abstract available.

5

Clinical approach to the diagnosis and treatment of cystic fibrosis and CFTR-related disorders.

Michl RK, Tabori H, Hentschel J, Beck JF, Mainz JG. Michl RK, et al. Among authors: mainz jg. Expert Rev Respir Med. 2016 Nov;10(11):1177-1186. doi: 10.1080/17476348.2016.1240032. Epub 2016 Oct 12. Expert Rev Respir Med. 2016. PMID: 27653767

6

Abdominal symptoms in cystic fibrosis and their relation to genotype, history, clinical and laboratory findings.

Tabori H, Arnold C, Jaudszus A, Mentzel HJ, Renz DM, Reinsch S, Lorenz M, Michl R, Gerber A, Lehmann T, Mainz JG. Tabori H, et al. Among authors: mainz jg. PLoS One. 2017 May 4;12(5):e0174463. doi: 10.1371/journal.pone.0174463. eCollection 2017. PLoS One. 2017. PMID: 28472055 Free PMC article.

7

Effects of Ivacaftor in Three Pediatric Siblings With Cystic Fibrosis Carrying the Mutations G551D And F508del.

Mainz JG, Arnold C, Hentschel J, Tabori H. Mainz JG, et al. Arch Bronconeumol (Engl Ed). 2018 Apr;54(4):232-234. doi: 10.1016/j.arbres.2017.09.012. Epub 2017 Nov 3. Arch Bronconeumol (Engl Ed). 2018. PMID: 29103672 English, Spanish. No abstract available.

8

Relation of Ultrasound Findings and Abdominal Symptoms obtained with the CFAbd-Score in Cystic Fibrosis Patients.

Tabori H, Jaudszus A, Arnold C, Mentzel HJ, Lorenz M, Michl RK, Lehmann T, Renz DM, Mainz JG. Tabori H, et al. Among authors: mainz jg. Sci Rep. 2017 Dec 12;7(1):17465. doi: 10.1038/s41598-017-17302-4. Sci Rep. 2017. PMID: 29234058 Free PMC article.

9

Validity and Reliability of a Novel Multimodal Questionnaire for the Assessment of Abdominal Symptoms in People with Cystic Fibrosis (CFAbd-Score).

Jaudszus A, Zeman E, Jans T, Pfeifer E, Tabori H, Arnold C, Michl RK, Lorenz M, Beiersdorf N, Mainz JG. Jaudszus A, et al. Among authors: mainz jg. Patient. 2019 Aug;12(4):419-428. doi: 10.1007/s40271-019-00361-2. Patient. 2019. PMID: 30887269

10

Patient-reported outcomes in patients with cystic fibrosis with a G551D mutation on ivacaftor treatment: results from a cross-sectional study.

Bell SC, Mainz JG, MacGregor G, Madge S, Macey J, Fridman M, Suthoff ED, Narayanan S, Kinnman N. Bell SC, et al. Among authors: mainz jg. BMC Pulm Med. 2019 Aug 13;19(1):146. doi: 10.1186/s12890-019-0887-6. BMC Pulm Med. 2019. PMID: 31409396 Free PMC article.

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