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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1955 1
1957 2
2007 1
2008 4
2009 3
2010 2
2011 1
2012 2
2013 2
2014 1
2015 6
2016 6
2017 2
2019 2
2024 0

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33 results

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Page 1
Lung disease caused by ABCA3 mutations.
Kröner C, Wittmann T, Reu S, Teusch V, Klemme M, Rauch D, Hengst M, Kappler M, Cobanoglu N, Sismanlar T, Aslan AT, Campo I, Proesmans M, Schaible T, Terheggen-Lagro S, Regamey N, Eber E, Seidenberg J, Schwerk N, Aslanidis C, Lohse P, Brasch F, Zarbock R, Griese M. Kröner C, et al. Among authors: zarbock r. Thorax. 2017 Mar;72(3):213-220. doi: 10.1136/thoraxjnl-2016-208649. Epub 2016 Aug 11. Thorax. 2017. PMID: 27516224
[Pseudoxanthoma elasticum--case report].
Finger RP, Hendig D, Götting C, Charbel Issa P, Zarbock R, Scholl HN, Holz FG. Finger RP, et al. Among authors: zarbock r. MMW Fortschr Med. 2011 Feb 17;153(7):38-9. MMW Fortschr Med. 2011. PMID: 21648140 German. No abstract available.
Surfactant proteins in pediatric interstitial lung disease.
Griese M, Lorenz E, Hengst M, Schams A, Wesselak T, Rauch D, Wittmann T, Kirchberger V, Escribano A, Schaible T, Baden W, Schulze J, Krude H, Aslanidis C, Schwerk N, Kappler M, Hartl D, Lohse P, Zarbock R. Griese M, et al. Among authors: zarbock r. Pediatr Res. 2016 Jan;79(1-1):34-41. doi: 10.1038/pr.2015.173. Epub 2015 Sep 16. Pediatr Res. 2016. PMID: 26375475
Homooligomerization of ABCA3 and its functional significance.
Frixel S, Lotz-Havla AS, Kern S, Kaltenborn E, Wittmann T, Gersting SW, Muntau AC, Zarbock R, Griese M. Frixel S, et al. Among authors: zarbock r. Int J Mol Med. 2016 Aug;38(2):558-66. doi: 10.3892/ijmm.2016.2650. Epub 2016 Jun 21. Int J Mol Med. 2016. PMID: 27352740
Surfactant lipidomics in healthy children and childhood interstitial lung disease.
Griese M, Kirmeier HG, Liebisch G, Rauch D, Stückler F, Schmitz G, Zarbock R; ILD-BAL working group of the Kids-Lung-Register. Griese M, et al. Among authors: zarbock r. PLoS One. 2015 Feb 18;10(2):e0117985. doi: 10.1371/journal.pone.0117985. eCollection 2015. PLoS One. 2015. PMID: 25692779 Free PMC article.
Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patients.
Kröner C, Reu S, Teusch V, Schams A, Grimmelt AC, Barker M, Brand J, Gappa M, Kitz R, Kramer BW, Lange L, Lau S, Pfannenstiel C, Proesmans M, Seidenberg J, Sismanlar T, Aslan AT, Werner C, Zielen S, Zarbock R, Brasch F, Lohse P, Griese M. Kröner C, et al. Among authors: zarbock r. Eur Respir J. 2015 Jul;46(1):197-206. doi: 10.1183/09031936.00129414. Epub 2015 Feb 5. Eur Respir J. 2015. PMID: 25657025 Free article.
33 results