Browsing by Author "Özdemir, Gül Nihal"
Now showing items 1-9 of 9
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A case of bartonellosis mimicking systemic lupus erythematosus
Kara, Manolya; Özdemir, Gül Nihal; Taşdemir, Mehmet; Ata, Serap; Karini, Belma; Valiyev, Eldar; Tutkun, İlknur Tuğal; Köse, Gülşen; Özkaya, Ozan (SAGE PUBLICATIONS LTD, 2022)Background and aim: Cat-scratch disease (CSD) is a systemic bacterial infection caused by Bartonella henselae. The disease is typically characterized by regional lymphadenopathy developing after scratches from domestic or ... -
Clinical features and outcome of children with hereditary spherocytosis
Kılıç, Mehmet A; Özdemir, Gül 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
Özdemir, Gül 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 ... -
Dasatinib-related pleural effusion and lymphocytosis rates are different between adult and pediatric patients with Philadelphia chromosome-positive leukemias: are age and comorbidities only to blame?
Kılıçarslan, Necati Alp; Börekçi, Şermin; Özdemir, Gül Nihal; Sayitoğlu, Müge; Eskazan, Ahmet Emre (Taylor and Francis, 2022)No Abstract Available -
Gaucher disease for the hematologists
Özdemir, Gül Nihal; Gündüz, 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; Özbek, 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
Akça, Tuğberk; Ayçiçek, Ali; Özkaya, Güven; Özdemir, Gül 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
Gündüz, Eren; Özdemir, Gül Nihal; Bakanay, Şule Mine; Karakuş, 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, Tuğce; Erbilgin, Yücel; Hatırnaz, Özden; Karaman, Serap; Karakaş, Zeynep; Küçükcankurt, Fulya; Celkan, Tülin Tiraje; Timur, Çetin; Özdemir, Gül Nihal; Hacısalihoglu, Sadan; Aylan Gelen, Sema; Sayitoğlu, Müge (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 ...
