Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene
Journal Title: Turkish Journal of Hematology - Year 2015, Vol 32, Issue 3
Abstract
Authors and Affiliations
Fatih Demircioğlu, Mustafa Erkoçoğlu, Mervan Bekdaş, Sevil Göksügür, Semra Büyükkorkmaz, Seher Açar
Glomerular and Tubular Functions in Children and Adults with Transfusion-Dependent Thalassemia
This study aimed at assessing renal functions in patients with transfusion-dependent thalassemia (TDT). Fifty patients and 30 controls were enrolled in this prospective study. Serum levels of electrolytes and albumin wer...
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...
Thrombotic Microangiopathy with Complement Factor H Gene Mutations Unassociated with Atypical Hemolytic Uremic Syndrome
Implementation of an ISBT 128-Compatible Medical Record System to Facilitate Traceability of Stem Cell Products
To the Editor,
A Case of Anaplastic Lymphoma Kinase-positive Large B-cell Lymphoma
.