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Toplam kayıt 18, listelenen: 1-10
Where do these guests come from? A diagnostic approach for metastatic lymph nodes
(Aves, 2018)
Objective: In cases presenting with lymphadenopathies (LAP) without a primary focus detected by simple radiological methods, the primary tumor can be diagnosed by a histopathological evaluation of the metastatic lymph ...
A multicenter experience of thrombotic microangiopathies in Turkey: The Turkish Hematology Research and Education Group (ThREG)-TMA01 study
(Pergamon-Elsevier Science Ltd, 2018)
Thrombotic microangiopathies (TMAs) are rare, but life-threatening disorders characterized by microangiopathic hemolytic anemia and thrombocytopenia (MAHAT) associated with multiorgan dysfunction as a result of microvascular ...
Heart Rate Recovery as a Novel Test for Predicting Cardiac Involvement in Beta-Thalassemia Major
(Taiwan Soc Cardiology, 2017)
Background: Abnormal heart rate recovery (HRR) is predictive of cardiac mortality. Autonomic abnormalities in beta-thalassemia major (TM) patients have been reported in previous studies. However, the importance of low HRR ...
Analysis of Skin, Hair and Nail Diseases in the Adults with Beta Thalassemia Major
(Gazi Univ, Fac Med, 2018)
Objective: beta-thalassemia major (BTM) is a genetic disorder necessitating frequent blood transfusions, which is characterized by functional and physiological disorders in multiple organs. We aimed to research the prevalence ...
Acquired hemophilia A in chronic lymphocytic leukemia: A case report
(Pergamon-Elsevier Science Ltd, 2019)
Acquired hemophilia A, due to spontaneous autoantibody against FVIII, is a rare hemorrhagic disorder with an incidence of about 1 per million population per year. If unrecognized and untreated, it is associated with a high ...
beta-Thalassemia gene mutations in Antalya, Turkey: results from a single centre study
(Taylor & Francis Ltd, 2016)
beta-Thalassemia (beta-thal) is a common autosomal recessive disorder resulting from over 300 different mutations of the beta-globin genes. Our aim was to create a mutation map of beta-thal in the province of Antalya, ...
beta 2-Microglobulin, Neutrophil Gelatinase-Associated Lipocalin, and Endocan Values in Evaluating Renal Functions in Patients with beta-Thalassemia Major
(Taylor & Francis Ltd, 2020)
Chronic anemia, transfusion-associated iron deposition, and chelating agents lead to renal impairment in beta-thalassemia (beta-thal) patients. The present study aimed to determine the most reliable and practical method ...
Synchronous Presentation of Two Extranodal Lymphomas: Follicular Lymphoma and Extranodal Marginal Zone Lymphoma of the Mucosa-Associated Lymphoid Tissue (MALToma)
(De Gruyter Open Ltd, 2018)
Synchronous malignancies are rare conditions in oncology practices, generally seen as solid tumors with hematological neoplasms. However, occurrence of two different hematological malignancies in the same patient is extremely ...
Clinical characteristics and therapeutic outcomes of paroxysmal nocturnal hemoglobinuria patients in Turkey: a multicenter experience
(Springer, 2021)
The aim of this study is to collect paroxysmal nocturnal hemoglobinuria (PNH) patient data from hematology centers all over Turkey in order to identify clinical features and management of PNH patients. Patients with PNH ...
Evaluation of Iron Overload in the Heart and Liver Tissue by Magnetic Resonance Imaging and its Relation to Serum Ferritin and Hepcidin Concentrations in Patients with Thalassemia Syndromes
(Springer India, 2017)
Iron overload is one of the major prognostic factor in thallassemia patients. We aimed to evaluate iron accumulation in the heart and liver by MRI in thalassemia major, thalassemia intermedia, and S- thalassemia patients ...