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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 1
1997 1
1998 1
2000 2
2001 4
2002 1
2003 3
2004 6
2005 3
2009 2
2010 1
2011 2
2013 3
2014 4
2015 3
2016 2
2017 1
2018 2
2019 2
2020 2
2021 0
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42 results
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Page 1
Outcomes of Eltrombopag Treatment and Development of Iron Deficiency in Children with Immune Thrombocytopenia in Turkey.
Koca Yozgat A, Leblebisatan G, Akbayram S, Çınar Özel S, Karakaş Z, Erduran E, Yılmaz Ş, Koçak Ü, Ünal Ş, Özdemir GN, Albayrak M, Zengin E, Oymak Y, Bör Ö, Çakmaklı HF, Söker M, Gürlek Gökçebay D, Tokgöz H, Malbora B, Karaman S, Celkan T, Şaşmaz İ, Yaralı N, Ören H, Ünüvar A, Özbek NY. Koca Yozgat A, et al. Among authors: soker m. Turk J Haematol. 2020 Aug 28;37(3):139-144. doi: 10.4274/tjh.galenos.2020.2019.0380. Epub 2020 Mar 17. Turk J Haematol. 2020. PMID: 32181630 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: soker m. Pediatr Blood Cancer. 2019 Oct;66(10):e27923. doi: 10.1002/pbc.27923. Epub 2019 Jul 19. Pediatr Blood Cancer. 2019. PMID: 31321910
Hereditary spherocytosis: evaluation of 68 children.
Konca Ç, Söker M, Taş MA, Yıldırım R. Konca Ç, et al. Among authors: soker m. Indian J Hematol Blood Transfus. 2015 Mar;31(1):127-32. doi: 10.1007/s12288-014-0379-z. Epub 2014 Apr 11. Indian J Hematol Blood Transfus. 2015. PMID: 25548458 Free PMC article.
A rare cause of recurrent oral lesions: chediak-higashi syndrome.
Karabel M, Kelekçi S, Sen V, Karabel D, Aliosmanoğlu C, Söker M. Karabel M, et al. Among authors: soker m. Turk J Haematol. 2014 Sep 5;31(3):313-4. doi: 10.4274/tjh.2013.0282. Turk J Haematol. 2014. PMID: 25330529 Free PMC article. No abstract available.
Urinary Kidney Injury Molecules in Children with Iron-Deficiency Anemia.
Güneş A, Ece A, Aktar F, Tan İ, Söker M, Karabel D, Balık H, Uluca Ü, Şen V, Yolbaş İ. Güneş A, et al. Among authors: soker m. Med Sci Monit. 2015 Dec 24;21:4023-9. doi: 10.12659/msm.896794. Med Sci Monit. 2015. PMID: 26697893 Free PMC article.
Deferasirox in children with transfusion-dependent thalassemia or sickle cell anemia: A large cohort real-life experience from Turkey (REACH-THEM).
Antmen B, Karakaş Z, Yeşilipek MA, Küpesiz OA, Şaşmaz İ, Uygun V, Kurtoğlu E, Oktay G, Aydogan G, Akın M, Salcioglu Z, Vergin C, Kazancı EG, Ünal S, Çalışkan Ü, Aral YZ, Türkkan E, Meral Güneş A, Tunç B, Gümrük F, Ayhan AC, Söker M, Koç A, Oymak Y, Ertem M, Timur Ç, Yıldırmak Y, İrken G, Apak H, Biner B, Eren TG, Işık Balcı Y, Koçak Ü, Karasu G, Akkaynak D, Patıroğlu T. Antmen B, et al. Among authors: soker m. Eur J Haematol. 2019 Feb;102(2):123-130. doi: 10.1111/ejh.13180. Epub 2018 Dec 9. Eur J Haematol. 2019. PMID: 30300449
Amitraz poisoning in children.
Yaramis A, Soker M, Bilici M. Yaramis A, et al. Among authors: soker m. Hum Exp Toxicol. 2000 Aug;19(8):431-3. doi: 10.1191/096032700682694215. Hum Exp Toxicol. 2000. PMID: 11125712
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