Spinal Cord Compression And Extramedullary Hematopoiesis in Young Egyptian β-thalassemia Patients
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630260903337451
Reference24 articles.
1. Identification of Mediterranean β-Thalassemia Mutations by Reverse DOT-Blot in Italians and Egyptians
2. Identification of novel Asian Indian and Japanese mutations causing β-thalassaemia in the Egyptian population
3. Lumbar nerve root compression due to extramedullary hemopoiesis in a patient with thalassemia: complete clinical regression with radiation therapy
4. Spinal cord compression due to extramedullary haematopoiesis in two patients with thalassaemia: complete regression with blood transfusion therapy
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2. Epidemiologic study of major complications in adolescent and adult patients with thalassemia in Northeastern Thailand: the E-SAAN study phase I;Hematology;2017-07-31
3. Non-transfusion-dependent thalassemia and thalassemia intermedia: epidemiology, complications, and management;Current Medical Research and Opinion;2015-11-25
4. Extramedullary hematopoiesis of the liver in a child with sickle cell disease: A rare complication;Pediatrics International;2015-07-14
5. Clinicopathological and Radiological Study of Egyptian β-Thalassemia Intermedia and β-Thalassemia Major Patients: Relation to Complications and Response to Therapy;Hemoglobin;2011-07-28
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