Methyltetrahydrofolate Reductase C677T Mutation and 4G/5G Plasminogen Activator Inhibitor-1 Polymorphism in a Child with Deep Vein Thrombosis
Journal Title: Iranian Journal of Blood and Cancer - Year 2009, Vol 1, Issue 4
Abstract
This article has no abstract.
Authors and Affiliations
Peyman Eshghi, Kourosh Goudarzi Pour, Roxana Aghakhani
Students’ Research Committee (SRC), Baqiyatallah University of Medical Sciences, Tehran, Iran
This article has no abstract.
Use of Capillary Electrophoresis for Detection of Hemoglobinopathies in Individuals Referred to Health Centers in Masjed-Soleiman
Background: Hemoglobinopathies are the commonest single gene disorder in human that affect hemoglobin production and function that occur when mutations alter the amino acid sequence of globin chains. The purpose of the p...
Breast Cancer Associated with Dermatomyositis
Dermatomyositis (DM) is a rare idiopathic inflammatory myopathy with characteristic skin lesions. Case series have shown an association between dermatomyositis and malignancy. Malignancy has been found in 15-25% of the a...
Synovial Sarcoma of the Head and Neck: A Case of Childhood Soft Tissue Sarcoma
Although rare, synovial sarcoma is the most common malignant non-rhabdomyosarcomatous soft tissue sarcoma in children and adolescents. Synovial sarcoma typically involves the soft tissues of the extremities, especially n...
Applying Totally Implantable Venous Access Devices (TIVAD) in Children: the First Iranian Experience
Background:During recent years and paralleling the advances in the treatment of patients requiring chem-otherapy or long-term total parenteral nutrition (TPN), it has been necessary to provide a chronic central venous ac...