Thrombotic Microangiopathy with Complement Factor H Gene Mutations Unassociated with Atypical Hemolytic Uremic Syndrome
Journal Title: Turkish Journal of Hematology - Year 2015, Vol 32, Issue 3
Abstract
Authors and Affiliations
Yeşim Oymak, Tuba Karapınar, Yılmaz Ay, Esin Özcan, Neryal Müminoğlu, Sultan Aydın Köker, Ersin Töret, Afig Berdeli, Erkin Serdaroğlu, Canan Vergin
An Updated Review of Abnormal Hemoglobins in the Turkish Population
The Clinical Significance of Schistocytes: A Prospective Evaluation of the International Council for Standardization in Hematology Schistocyte Guidelines
Objective: The presence of ≥1% schistocytes on a peripheral blood smear (PBS) is an important criterion for the diagnosis of thrombotic microangiopathy (TMA). The reporting of schistocytes has been standardized by the In...
B-Cell Chronic Lymphocytic Leukemia and Colon Adenocarcinoma in the Same Mesenteric Lymph Node
A50-year-old male patient presented with microcytic anemia (hemoglobin: 10.2 g/dL, hematocrit: 33.8%, mean corpuscular volume: 64 fL), leukocytosis of 19.7 x 109/L (lymphocytes of 51.2%, 10x109/L), and normal platelet co...
Yenidoğan Döneminde Intraabdominal Kanama ile Erken Postnatal Hemorajik Şoka Neden Olan Hemofili A Vakası
Three Novel Calreticulin Mutations in Two Turkish Patients
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