Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

128 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
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: aslanidis c. Thorax. 2017 Mar;72(3):213-220. doi: 10.1136/thoraxjnl-2016-208649. Epub 2016 Aug 11. Thorax. 2017. PMID: 27516224
Association of HDL deficiency with a novel mutation in the ABCA1 gene.
Denk GU, Aslanidis C, Schmitz G, Parhofer KG, Pusl T. Denk GU, et al. Among authors: aslanidis c. Exp Clin Endocrinol Diabetes. 2011 Jan;119(1):53-5. doi: 10.1055/s-0030-1254138. Epub 2010 Jun 8. Exp Clin Endocrinol Diabetes. 2011. PMID: 20533173
Alteration of the pulmonary surfactant system in full-term infants with hereditary ABCA3 deficiency.
Brasch F, Schimanski S, Mühlfeld C, Barlage S, Langmann T, Aslanidis C, Boettcher A, Dada A, Schroten H, Mildenberger E, Prueter E, Ballmann M, Ochs M, Johnen G, Griese M, Schmitz G. Brasch F, et al. Among authors: aslanidis c. Am J Respir Crit Care Med. 2006 Sep 1;174(5):571-80. doi: 10.1164/rccm.200509-1535OC. Epub 2006 May 25. Am J Respir Crit Care Med. 2006. PMID: 16728712
Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3.
Wittmann T, Frixel S, Höppner S, Schindlbeck U, Schams A, Kappler M, Hegermann J, Wrede C, Liebisch G, Vierzig A, Zacharasiewicz A, Kopp MV, Poets CF, Baden W, Hartl D, van Kaam AH, Lohse P, Aslanidis C, Zarbock R, Griese M. Wittmann T, et al. Among authors: aslanidis c. Mol Med. 2016 Sep;22:183-191. doi: 10.2119/molmed.2015.00244. Epub 2016 Feb 26. Mol Med. 2016. PMID: 26928390 Free PMC article.
Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis.
Kleinlein B, Griese M, Liebisch G, Krude H, Lohse P, Aslanidis C, Schmitz G, Peters J, Holzinger A. Kleinlein B, et al. Among authors: aslanidis c. Arch Dis Child Fetal Neonatal Ed. 2011 Nov;96(6):F453-6. doi: 10.1136/adc.2009.180448. Epub 2010 Jun 28. Arch Dis Child Fetal Neonatal Ed. 2011. PMID: 20584796
Tools to explore ABCA3 mutations causing interstitial lung disease.
Wittmann T, Schindlbeck U, Höppner S, Kinting S, Frixel S, Kröner C, Liebisch G, Hegermann J, Aslanidis C, Brasch F, Reu S, Lasch P, Zarbock R, Griese M. Wittmann T, et al. Among authors: aslanidis c. Pediatr Pulmonol. 2016 Dec;51(12):1284-1294. doi: 10.1002/ppul.23471. Epub 2016 May 13. Pediatr Pulmonol. 2016. PMID: 27177387
128 results