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Year Number of Results
2015 5
2016 4
2017 2
2018 1
2019 2
2020 2
2023 1
2024 0

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14 results

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Page 1
ABCA3-related interstitial lung disease beyond infancy.
Li Y, Seidl E, Knoflach K, Gothe F, Forstner ME, Michel K, Pawlita I, Gesenhues F, Sattler F, Yang X, Kroener C, Reu-Hofer S, Ley-Zaporozhan J, Kammer B, Krüger-Stollfuß I, Dinkel J, Carlens J, Wetzke M, Moreno-Galdó A, Torrent-Vernetta A, Lange J, Krenke K, Rumman N, Mayell S, Sismanlar T, Aslan A, Regamey N, Proesmans M, Stehling F, Naehrlich L, Ayse K, Becker S, Koerner-Rettberg C, Plattner E, Manali ED, Papiris SA, Campo I, Kappler M, Schwerk N, Griese M. Li Y, et al. Among authors: sismanlar t. Thorax. 2023 Jun;78(6):587-595. doi: 10.1136/thorax-2022-219434. Epub 2023 Feb 20. Thorax. 2023. PMID: 36808083 Free PMC article.
Left upper lobe atelectasis due to plastic bronchitis.
Şişmanlar T, Aslan AT, Öztunalı Ç, Boyunağa Ö. Şişmanlar T, et al. Turk J Pediatr. 2017;59(2):207-209. doi: 10.24953/turkjped.2017.02.016. Turk J Pediatr. 2017. PMID: 29276877 Free article.
An adolescent case of extensive Behçet`s disease successfully treated with Infliximab.
Isıyel E, Bakkaloğlu S, Oğuz D, Yenicesu İ, Boyunağa Ö, Özdemir Y, Damar Ç, Kandur Y, Akçaboy M, Aslan AT, Şişmanlar T, Hasanoğlu E, Buyan N. Isıyel E, et al. Among authors: sismanlar t. Turk J Pediatr. 2019;61(4):585-588. doi: 10.24953/turkjped.2019.04.016. Turk J Pediatr. 2019. PMID: 31990477 Free article.
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: sismanlar t. Thorax. 2017 Mar;72(3):213-220. doi: 10.1136/thoraxjnl-2016-208649. Epub 2016 Aug 11. Thorax. 2017. PMID: 27516224
Persistent tachypnea of infancy: Follow up at school age.
Seidl E, Carlens J, Schwerk N, Wetzke M, Marczak H, Lange J, Krenke K, Mayell SJ, Escribano A, Seidenberg J, Ahrens F, Hebestreit H, Nährlich L, Sismanlar T, Aslan AT, Snijders D, Ullmann N, Kappler M, Griese M. Seidl E, et al. Among authors: sismanlar t. Pediatr Pulmonol. 2020 Nov;55(11):3119-3125. doi: 10.1002/ppul.25004. Epub 2020 Aug 13. Pediatr Pulmonol. 2020. PMID: 32761949
An unusual cause of stridor: congenital laryngeal web.
Derinöz O, Şişmanlar T. Derinöz O, et al. Among authors: sismanlar t. Turk Pediatri Ars. 2018 Sep 1;53(3):185-188. doi: 10.5152/TurkPediatriArs.2017.3922. eCollection 2018 Sep. Turk Pediatri Ars. 2018. PMID: 30459518 Free PMC article.
Cystic fibrosis in Turkey: First data from the national registry.
Dogru D, Çakır E, Şişmanlar T, Çobanoğlu N, Pekcan S, Cinel G, Yalçın E, Kiper N, Şen V, S Şen H, Ercan Ö, Keskin Ö, B Eltan S, Al Shadfan LM, Yazan H, Altıntaş DU, Şaşihüseyinoğlu Ş, Sapan N, Çekiç Ş, Çokuğraş H, A Kılınç A, R Gürsoy T, Aslan AT, Bingöl A, Başaran AE, Özdemir A, Köse M, Hangül M, Emiralioğlu N, Tuğcu G, Yüksel H, Yılmaz Ö, Orhan F, Gayretli Aydın ZG, Topal E, Tamay Z, Süleyman A, Can D, Bal CM, Çaltepe G, Özçelik U. Dogru D, et al. Among authors: sismanlar t. Pediatr Pulmonol. 2020 Feb;55(2):541-548. doi: 10.1002/ppul.24561. Epub 2019 Nov 11. Pediatr Pulmonol. 2020. PMID: 31710166
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: sismanlar t. 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.
14 results