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HAX1-related congenital neutropenia: Long-term observation in paediatric and adult patients enrolled in the European branch of the Severe Chronic Neutropenia International Registry (SCNIR).
Pogozhykh D, Yilmaz Karapinar D, Klimiankou M, Gerschmann N, Ebetsberger-Dachs G, Palmblad J, Carlsson G, Masmas T, Kinsey S, Bartels M, Mellor-Heineke S, Welte K, Skokowa J, Zeidler C. Pogozhykh D, et al. Among authors: yilmaz karapinar d. Br J Haematol. 2023 Jul;202(2):393-411. doi: 10.1111/bjh.18840. Epub 2023 May 16. Br J Haematol. 2023. PMID: 37193639
HAX1 mutation positive children presenting with haemophagocytic lymphohistiocytosis.
Karapınar TH, Yılmaz Karapinar D, Oymak Y, Ay Y, Demirağ B, Aykut A, Onay H, Hazan F, Aydınok Y, Özkınay F, Vergin C. Karapınar TH, et al. Among authors: yilmaz karapinar d. Br J Haematol. 2017 May;177(4):597-600. doi: 10.1111/bjh.14574. Epub 2017 Feb 7. Br J Haematol. 2017. PMID: 28169428 Free 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: yilmaz s, yilmaz b, karapinar th. Pediatr Blood Cancer. 2019 Oct;66(10):e27923. doi: 10.1002/pbc.27923. Epub 2019 Jul 19. Pediatr Blood Cancer. 2019. PMID: 31321910
Fertility in Patients with Thalassemia and Outcome of Pregnancies: A Turkish Experience.
Akıncı B, Yaşar AŞ, Özdemir Karadaş N, Önder Siviş Z, Hekimci Özdemir H, Yılmaz Karapınar D, Balkan C, Kavaklı K, Aydınok Y. Akıncı B, et al. Among authors: yilmaz karapinar d. Turk J Haematol. 2019 Nov 18;36(4):274-277. doi: 10.4274/tjh.galenos.2019.2019.0025. Epub 2019 Jun 14. Turk J Haematol. 2019. PMID: 31198015 Free PMC article.
A Novel Homozygous TRNT1 Mutation in a Child With an Early Diagnosis of Common Variable Immunodeficiency Leading to Mild Hypogammaglobulinemia and Hemolytic Anemia.
Topyildiz E, Edeer Karaca N, Bas I, Aykut A, Durmaz A, Guven Bilgin RB, Aksu G, Yilmaz Karapinar D, Kutukculer N. Topyildiz E, et al. Among authors: yilmaz karapinar d. J Pediatr Hematol Oncol. 2021 Aug 1;43(6):e780-e784. doi: 10.1097/MPH.0000000000002101. J Pediatr Hematol Oncol. 2021. PMID: 33843817
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