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
Bortezomib İlişkili Ortostatik Hipotansiyon ve Hiponatremi
The Effect of Hyperparathyroid State on Platelet Functions and Bone Loss
Objective: Coagulation and fibrinolysis defects were reported in primary hyperparathyroid patients. However, there are not enough data regarding platelet functions in this group of patients. Our aim was to evaluate the p...
Successful Treatment of Refractory Diamond-Blackfan Anemia Using Metoclopramide and Prednisolone
To the Editor, Diamond-Blackfan anemia (DBA) is a rare congenital hypoplastic anemia characterized by severe normochromic-macrocytic anemia, reticulocytopenia, a decrease in the number or absence of bone marrow erythroi...
Post-Partum Yumurtalık Ven Trombozu: Enfeksiyon ve Faktör V Leiden Mutasyonunun Birleşik Etkisi
A Rare Cause of Paraplegia: Myeloid Sarcoma
.