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A child presenting with hypercalcemia.
Çelik E, Özdemir GN, Tüysüz G, Taştan Y, Çam H, Celkan T. Çelik E, et al. Among authors: celkan t. Turk Pediatri Ars. 2014 Mar 1;49(1):81-3. doi: 10.5152/tpa.2014.661. eCollection 2014 Mar. Turk Pediatri Ars. 2014. PMID: 26078638 Free PMC article. No abstract available.
An infant with chronic hemolytic anemia.
Tüysüz G, Özdemir GN, Celkan T. Tüysüz G, et al. Among authors: celkan t. Turk Pediatri Ars. 2014 Sep 1;49(3):264-8. doi: 10.5152/tpa.2014.1813. eCollection 2014 Sep. Turk Pediatri Ars. 2014. PMID: 26078675 Free PMC article. No abstract available.
A rare cause of thrombocyte dysfunction: Hermansky-Pudlak syndrome.
Özdemir N, Çelik E, Başlar Z, Celkan T. Özdemir N, et al. Among authors: celkan t. Turk Pediatri Ars. 2014 Jun 1;49(2):163-6. doi: 10.5152/tpa.2014.1071. eCollection 2014 Jun. Turk Pediatri Ars. 2014. PMID: 26078655 Free PMC article.
Spontaneous splenic rupture in a patient with congenital afibrinogenemia.
Arcagök BC, Özdemir N, Tekin A, Özcan R, Eliçevik M, Şenyüz OF, Çam H, Celkan T. Arcagök BC, et al. Among authors: celkan t. Turk Pediatri Ars. 2014 Sep 1;49(3):247-9. doi: 10.5152/tpa.2014.1070. eCollection 2014 Sep. Turk Pediatri Ars. 2014. PMID: 26078670 Free PMC article.
Childhood mastocytosis: results of a single center.
Tüysüz G, Özdemir N, Apak H, Kutlubay Z, Demirkesen C, Celkan T. Tüysüz G, et al. Among authors: celkan t. Turk Pediatri Ars. 2015 Jun 1;50(2):108-13. doi: 10.5152/tpa.2015.2332. eCollection 2015 Jun. Turk Pediatri Ars. 2015. PMID: 26265895 Free PMC article.
Five-year-old girl with tongue bleeding.
Kızılocak H, Özdemir N, Varol F, Koç BŞ, Dikme G, Çam H, Celkan T. Kızılocak H, et al. Among authors: celkan t. Turk Pediatri Ars. 2016 Jun 1;51(2):117-9. doi: 10.5152/TurkPediatriArs.2016.3458. eCollection 2016 Jun. Turk Pediatri Ars. 2016. PMID: 27489471 Free PMC article. No abstract available.
Wernicke's Encephalopathy in a Child with Acute Lymphoblastic Leukemia.
Kızılocak H, Özdemir GN, Dikme G, Haşıloğlu ZI, Celkan T. Kızılocak H, et al. Among authors: celkan t. Turk J Haematol. 2017 Mar 1;34(1):99-100. doi: 10.4274/tjh.2016.0044. Epub 2016 Sep 9. Turk J Haematol. 2017. PMID: 27612298 Free PMC article. No abstract available.
Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.
Yılmaz Karapınar D, Patıroğlu T, Metin A, Çalışkan Ü, Celkan T, Yılmaz B, Karakaş Z, Karapınar TH, Akıncı B, Özkınay F, Onay H, Yeşilipek MA, Akar HH, Tüysüz G, Tokgöz H, Özdemir GN, Aslan Kıykım A, Karaman S, Kılınç Y, Oymak Y, Küpesiz A, Olcay L, Keskin Yıldırım Z, Aydoğan G, Gökçe M, İleri T, Aral YZ, Bay A, Atabay B, Kaya Z, Söker M, Özdemir Karadaş N, Özbek U, Özsait Selçuk B, Özdemir HH, Uygun V, Tezcan Karasu G, Yılmaz Ş. Yılmaz Karapınar D, et al. Among authors: celkan t. Pediatr Blood Cancer. 2019 Oct;66(10):e27923. doi: 10.1002/pbc.27923. Epub 2019 Jul 19. Pediatr Blood Cancer. 2019. PMID: 31321910
Voriconazole induced bradycardia.
Uludağ D, Ozdemir N, Tüysüz G, Eroğlu AG, Celkan T. Uludağ D, et al. Among authors: celkan t. Pediatr Hematol Oncol. 2013 Oct;30(7):674-6. doi: 10.3109/08880018.2013.775616. Epub 2013 Mar 13. Pediatr Hematol Oncol. 2013. PMID: 23484777
152 results