Browsing by Author "Ozdemir, Gul Nihal"
Now showing items 1-7 of 7
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Clinical features and outcome of children with hereditary spherocytosis
Kılıç, Mehmet A; Ozdemir, Gul Nihal; Tahtakesen, Tuba Nur; Gökçe, Müge G.; Uysalol, Ezgi Paslı; Bayram, Cengiz; Ayçiçek, Ali; Aydoǧan, Gönül (Lippincott Williams and Wilkins, 2021)Objective: The aim of this study was to evaluate the demographics, clinical, and laboratory findings and treatment responses of patients with hereditary spherocytosis (HS). Materials and Methods: Data of children with HS ... -
Çocuklarda miyelodisplastik sendrom
Ozdemir, Gul Nihal (DergiPark, 2021)Miyelodisplastik sendrom (MDS); sitopeni, displazi ve inefektif eritropoyez ile karakterize klonal bir kök hücre bozukluğudur. Çocuklarda MDS erişkinlere göre oldukça nadir görülür. Miyelodisplastik sendromda en sık ... -
Gaucher disease for the hematologists
Ozdemir, Gul Nihal; Gunduz, Eren (Galenos Publication System, 2022)No Abstract Available. Özet Mevcut Değil. -
Hepatitis-associated aplastic anemia: etiology, clinical characteristics and outcome
Tüfekçi, Özlem; Özdemir, Hamiyet Hekimci; Malbora, Barış; Ozbek, Namık Yaşar; Yaralı, Neşe; Erdem, Arzu Yazal; Evim, Melike Sezgin; Özdemir, Gül Nihal (Lippincott Williams and Wilkins, 2021)Hepatitis-associated aplastic anemia (HAA) is a form of acquired aplastic anemia (AA) in which bone marrow failure develops after an acute attack of hepatitis. Bone marrow failure leading to AA is generally severe in cases ... -
Long-term results of splenectomy in transfusion-dependent thalassemia
Akca, Tugberk; Aycicek, Ali; Ozkaya, Guven; Ozdemir, Gul Nihal (Walters Kluwer, 2022)Splenectomy is indicated in transfusion-dependent thalassemia (TDT) only in certain situations. This study aimed to present the effectiveness, complications, and long-term follow-up results of splenectomy in children ... -
A rare lymphoproliferative disease: castleman disease
Gunduz, Eren; Ozdemir, Nihal; Bakanay, Sule Mine; Karakus, Sema (GALENOS YAYINCILIK, 2021)Castleman disease is a rare lymphoproliferative disease also known as angiofollicular lymph node hyperplasia. It is classified as hyaline vascular and plasmacytic variants histologically but characteristics of both types ... -
Zinc finger protein 384 ( ZNF384) impact on childhood mixed phenotype acute leukemia and B-cell precursor acute lymphoblastic leukemia
Sudutan, Tugce; Erbilgin, Yucel; Hatırnaz, Ozden; Karaman, Serap; Karakas, Zeynep; Kucukcankurt, Fulya; Celkan, Tiraje; Timur, Cetin; Ozdemir, Gul Nihal; Hacısalihoglu, Sadan; Aylan Gelen, Sema; Sayitoglu, Muge (Taylor and Francis, 2022)B-cell precursor acute lymphoblastic leukemia (BCP-ALL) is a heterogeneous malignancy and consists of several genetic abnormalities. Some of these abnormalities are used in clinics for risk calculation and treatment ...
