October-December 2018| Vol 9| Issue 4
Guide lines for management of adult histiocytic disease
BACKGROUND: Histiocytic disease is a diverse disease, characterized by multisystem involvement, diagnosis and management can be challenging. Guidelines are important tool to provide evidence-ba...
Hematopoietic stem cell transplantation in children with hemoglobinopathies: A single-center experience
INTRODUCTION: Hematopoietic stem cell transplantation (HSCT) is a curative treatment for children with serious hematological disorders including thalassemia major (TM) and sickle cell disease...
Evaluation of platelet aggregation in splenectomized beta-thalassemia major and intermedia patients
BACKGROUND: Platelet dysfunction may be one of the pathophysiologic complications in beta-thalassemia patients. However, the results obtained from the platelet aggregation vary in different typ...
Blood requisition and utilization practice in obstetric patients at tertiary care center from South India: A descriptive study
BACKGROUND: Although blood ordering is a common practice in surgical field, in obstetric patients too requests are commonly made to crossmatch units of blood for patients in whom bleeding is an...
Prevalence of von willebrand disease among university students in Riyadh, Saudi Arabia
BACKGROUND: von Willebrand disease (vWD) is the most common hereditary bleeding disorder, affecting up to 1% of the general population.
OBJECTIVES: Estimating the prevalence of vWD ...
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The journal is indexed with, or included in, the following:
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