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Page 1
Rare coagulation disorders: a retrospective analysis of 156 patients in Turkey.
Fışgın T, Balkan C, Celkan T, Kılınç Y, Türker M, Timur C, Gürsel T, Kürekçi E, Duru F, Küpesiz A, Olcay L, Yılmaz S, Ozgen U, Unüvar A, Oren H, Kavaklı K. Fışgın T, et al. Among authors: celkan t. Turk J Haematol. 2012 Mar;29(1):48-54. doi: 10.5505/tjh.2012.02418. Epub 2012 Mar 5. Turk J Haematol. 2012. PMID: 24744623 Free PMC article.
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
Hemophagocytic Lymphohistiocytosis.
Kaçar AG, Celkan TT. Kaçar AG, et al. Among authors: celkan tt. Balkan Med J. 2022 Sep 9;39(5):309-317. doi: 10.4274/balkanmedj.galenos.2022.2022-4-83. Epub 2022 Aug 15. Balkan Med J. 2022. PMID: 35965424 Free PMC article.
Clinical and laboratory data of primary hemophagocytic lymphohistiocytosis: A retrospective review of the Turkish Histiocyte Study Group.
Fışgın T, Patıroğlu T, Özdemir A, Celkan T, Çalışkan Ü, Ertem M, Yaralı N, Erduran E, Vergin C, Canpolat C, Duru F, Bay A, Özbek N, Yılmaz Karapınar D. Fışgın T, et al. Among authors: celkan t. Turk J Haematol. 2010 Dec 5;27(4):257-62. doi: 10.5152/tjh.2010.47. Turk J Haematol. 2010. PMID: 27263739 Free article. English.
153 results