Myeloperoksidaz Eksikliği, Boyanmamış Hücre Bayrağı Altındaki Gizem
Journal Title: Turkish Journal of Hematology - Year 2013, Vol 30, Issue 2
Abstract
Authors and Affiliations
Türkan Patıroğlu, Hatice Güngör, Julie Belohradsky, Ekrem Ünal, Christoph Klein
A Novel Mutation in a Child with Atypical Wiskott-Aldrich Syndrome Complicated by Cytomegalovirus Infection
.
A Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G
Objective: Hyperferritinemia cataract syndrome (HFCS) is an autosomal dominantly inherited disease characterized by increased serum ferritin levels and bilateral cataract formation in the early period of life. Heterozygo...
Diagnostic Testing for Differential Diagnosis in Thrombotic Microangiopathies
Thrombotic microangiopathies (TMAs) are multiple disease entities with different etiopathogeneses, characterized by thrombocytopenia, microangiopathic hemolytic anemia (MAHA) with schistocytosis, variable symptoms includ...
Wilms Tumor-1 (WT1) rs16754 Polymorphism and Clinical Outcome in Acute Myeloid Leukemia
.
Antioxidants Attenuate Oxidative Stress-Induced Hidden Blood Loss in Rats
Objective: Hidden blood loss (HBL), commonly seen after total knee or hip arthroplasty, causes postoperative anemia even after reinfusion or blood transfusion based on the visible blood loss volume. Recent studies demons...