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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: ozdemir gn. 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.
Variant Guillain-Barré syndrome in a patient with Hodgkin lymphoma: AMSAN.
Al IO, Koç B, Bayram C, Paslı EU, Yıldız EP, Ayçiçek A, Çalışkan M, Özdemir GN. Al IO, et al. Among authors: ozdemir gn. Turk Pediatri Ars. 2018 Dec 1;53(4):263-266. doi: 10.5152/TurkPediatriArs.2018.4763. eCollection 2018 Dec. Turk Pediatri Ars. 2018. PMID: 30872931 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: ozdemir gn, ozdemir hh, ozdemir karadas n. Pediatr Blood Cancer. 2019 Oct;66(10):e27923. doi: 10.1002/pbc.27923. Epub 2019 Jul 19. Pediatr Blood Cancer. 2019. PMID: 31321910
Clinical Features and Outcome of Children With Hereditary Spherocytosis.
Kiliç MA, Özdemir GN, Tahtakesen TN, Gökçe M, Uysalol EP, Bayram C, Ayçiçek A, Aydoğan G. Kiliç MA, et al. Among authors: ozdemir gn. J Pediatr Hematol Oncol. 2022 Mar 1;44(2):e306-e309. doi: 10.1097/MPH.0000000000002211. J Pediatr Hematol Oncol. 2022. PMID: 34054043
38 results