Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Akkız Şahin"'
Autor:
Kamuran Karaman, Eyüp Yürektürk, Hadi Geylan, Akkız Şahin Yaşar, Serap Karaman, Huri Sema Aymelek, Mecnun Çetin, Ahmet Fayik Oner
Publikováno v:
Platelets, Vol 32, Iss 2, Pp 238-242 (2021)
Glanzmann’s thrombasthenia (GT) is an autosomal recessive disorder in which the underlying problem is the lack or dysfunction of the GpIIb/IIIa receptor on the platelet surface. The present study determines the genetic mutation typology and analyze
Externí odkaz:
https://doaj.org/article/fd04d405f9504f739929fde27b30e2fe
Autor:
Deniz Yılmaz Karapınar, Akkız Şahin, Selime Özen, Pınar Yazıcı Özkaya, Zühal Önder Siviş, Ayşe Burcu Akıncı, Nihal Özdemir Karadaş, Bülent Karapınar
Publikováno v:
Journal of Pediatric Research, Vol 7, Iss 2, Pp 139-145 (2020)
Aim:Hyponatremia is a common electrolyte abnormality in hospitalized patients. Administration of isotonic maintenance fluids is recommended to prevent hyponatremia. The present study was conducted to evaluate the frequency and severity of hyponatremi
Externí odkaz:
https://doaj.org/article/3c29bed23a6040088c6710c9bab19d8d
Autor:
Burcu Akıncı, Hamiyet Hekimci Özdemir, Nihal Özdemir Karadaş, Akkız Şahin Yaşar, Zuhal Önder Siviş, Yeşim Aydınok, Kaan Kavaklı, Can Balkan, Deniz Yılmaz Karapınar
Publikováno v:
Journal of Pediatric Research, Vol 7, Iss 1, Pp 13-17 (2020)
Aim:Mastocytosis is a rare disease characterized by clonal mast cell proliferation in one or more organs. It can lead to different clinical manifestations and has no definitive treatment. In this study, we aimed to evaluate the clinical and laborator
Externí odkaz:
https://doaj.org/article/cf03b8c4e0c54198bf4228ff8f2efe42
Autor:
Burcu Akıncı, Akkız Şahin Yaşar, Nihal Özdemir Karadaş, Zuhal Önder Siviş, Hamiyet Hekimci Özdemir, Deniz Yılmaz Karapınar, Can Balkan, Kaan Kavaklı, Yeşim Aydınok
Publikováno v:
Turkish Journal of Hematology, Vol 36, Iss 4, Pp 274-277 (2019)
Objective: In recent years, the rates of marriage and pregnancy are increasing in patients with thalassemia major. The aim of the present study was to investigate the fertility rate of thalassemic patients and the course of pregnancies in terms of mo
Externí odkaz:
https://doaj.org/article/07af9770e5bf4ad0a6e911ceca1b7519
Autor:
Nihal Karadaş, Kaan Kavakli, Burcu Akıncı, Zuhal Önder Siviş, Can Balkan, Deniz Yilmaz Karapinar, Akkız Şahin Yaşar, Hamiyet Hekimci Özdemir, Yesim Aydinok
Publikováno v:
Journal of Pediatric Research, Vol 7, Iss 1, Pp 13-17 (2020)
Aim: Mastocytosis is a rare disease characterized by clonal mast cell proliferation in one or more organs. It can lead to different clinical manifestations and has no definitive treatment. in this study, we aimed to evaluate the clinical and laborato
Autor:
Eyüp Yürektürk, Akkız Şahin Yaşar, Serap Karaman, Huri Sema Aymelek, Kamuran Karaman, Mecnun Çetin, Ahmet Fayik Öner, Hadi Geylan
Publikováno v:
Platelets. 32:238-242
Glanzmann's thrombasthenia (GT) is an autosomal recessive disorder in which the underlying problem is the lack or dysfunction of the GpIIb/IIIa receptor on the platelet surface. The present study determines the genetic mutation typology and analyzes
Autor:
Akıncı, Burcu1 bdeveci@windowslive.com, Yaşar, Akkız Şahin1, Karadaş, Nihal Özdemir1, Siviş, Zuhal Önder1, Özdemir, Hamiyet Hekimci1, Karapınar, Deniz Yılmaz1, Balkan, Can1, Kavaklı, Kaan1, Aydınok, Yeşim1
Publikováno v:
Turkish Journal of Hematology. 2019, Vol. 36 Issue 4, p274-277. 4p.
Autor:
Mecnun Çetin, Akkız Şahin Yaşar, Burcu Güven, Perihan Tunçdemir, Kamuran Karaman, Nevzat Turfan
Publikováno v:
Journal of Tropical Pediatrics. 65:474-480
ObjectiveTo investigate the effect of inflammation on the conducting system of the heart in patients diagnosed with brucellosis.MethodsA total of 42 patients diagnosed with brucellosis and 39 age and sex-matched healthy children were enrolled into th
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 70(6)
Objective Malnutrition is commonly seen in children with exocrine pancreatic insufficiency (EPI). Pancreatic enzyme replacement therapy (PERT) is the mainstay treatment of acute malnutrition in children detected with a disease closely associated with
Publikováno v:
Acibadem Universitesi Saglik Bilimleri Dergisi.
Langerhans hucreli histiositoz LHH , CD1a, langerin ve S100 proteini eksprese eden ve ultrastrikturel incelemede Birbeck granulleri varligi gosterilen, Langerhans tipi hucrelerin klonal neoplastik proliferasyonudur. Hastalik, klinik olarak cok degisk