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Glucose 6 phosphate dehydrogenase deficiency: A single-center experience.
Kılıç MA, Özdemir GN, Tahtakesen TN, Uysalol EP, Bayram C, Ayçiçek A, Aydoğan G. Kılıç MA, et al. Among authors: aydogan g. Turk Arch Pediatr. 2021 May 1;56(3):245-248. doi: 10.5152/TurkArchPediatr.2021.20042. eCollection 2021. Turk Arch Pediatr. 2021. PMID: 34104916 Free PMC article.
A National Registry of Thalassemia in Turkey: Demographic and Disease Characteristics of Patients, Achievements, and Challenges in Prevention.
Aydınok Y, Oymak Y, Atabay B, Aydoğan G, Yeşilipek A, Ünal S, Kılınç Y, Oflaz B, Akın M, Vergin C, Sezgin Evim M, Çalışkan Ü, Ünal Ş, Bay A, Kazancı E, İleri T, Atay D, Patıroğlu T, Kahraman S, Söker M, Akcan M, Akdeniz A, Büyükavcı M, Alanoğlu G, Bör Ö, Soyer N, Özdemir Karadaş N, Uysalol E, Türker M, Akçay A, Ocak S, Güneş AM, Tokgöz H, Ünal E, Tiftik N, Karakaş Z. Aydınok Y, et al. Among authors: aydogan g. Turk J Haematol. 2018 Mar 1;35(1):12-18. doi: 10.4274/tjh.2017.0039. Epub 2017 Apr 13. Turk J Haematol. 2018. PMID: 28404539 Free PMC article.
Congenital Factor Deficiencies in Children: A Report of a Single-Center Experience.
Şalcıoğlu Z, Bayram C, Şen H, Ersoy G, Aydoğan G, Akçay A, Tuğcu D, Akıcı F, Gökçe M, Demirkaya M, Ayçiçek A, Başlar Z. Şalcıoğlu Z, et al. Among authors: aydogan g. Clin Appl Thromb Hemost. 2018 Sep;24(6):901-907. doi: 10.1177/1076029617731596. Epub 2017 Oct 19. Clin Appl Thromb Hemost. 2018. PMID: 29050499 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: aydogan g. Pediatr Blood Cancer. 2019 Oct;66(10):e27923. doi: 10.1002/pbc.27923. Epub 2019 Jul 19. Pediatr Blood Cancer. 2019. PMID: 31321910
A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome.
Odaman-Al I, Gezdirici A, Yıldız M, Ersoy G, Aydoğan G, Şalcıoğlu Z, Tahtakesen TN, Önal H, Küçükemre-Aydın B. Odaman-Al I, et al. Among authors: aydogan g. Turk J Pediatr. 2019;61(2):257-260. doi: 10.24953/turkjped.2019.02.015. Turk J Pediatr. 2019. PMID: 31951336 Free article.
Odaman-Al I, Gezdirici A, Yildiz M, Ersoy G, Aydogan G, Salcioglu Z, Tahtakesen TN, Onal H, Kucukemre-Aydin B. ...
Odaman-Al I, Gezdirici A, Yildiz M, Ersoy G, Aydogan G, Salcioglu Z, Tahtakesen TN, Onal H, Kucukemre-Aydin B. ...
70 results