60 International Journal of Modern Anthropology Int. J. Mod. Anthrop: 60-78 Available online at: www.ata.org.tn ;

First Page		Document Content
Date: 2012-05-17 11:27:37 Health Thalassemia Beta-thalassemia Hemoglobinopathy Hemoglobin Compound heterozygosity Alpha-thalassemia Sickle-cell disease Fetal hemoglobin Hemoglobins Medicine Biology		60 International Journal of Modern Anthropology Int. J. Mod. Anthrop: 60-78 Available online at: www.ata.org.tn ; Add to Reading List Source URL: www.ata.org.tn Download Document from Source Website File Size: 401,28 KB Share Document on Facebook

	2018 POSTER SESSION ABSTRACTS – GRADUATE STUDENTS 03 Kinesiophobia and Depression in Patients with Sickle Cell Disease Brianna J. Jones Faculty Advisor: Christopher L. Edwards, Ph.D. DocID: 1uCj8 - View Document
	GMI-1070: Reduction in Time to Resolution of Vaso-Occlusive Crisis and Decreased Opioid Use in a Prospective, Randomized, Multi-Center Double Blind, Adaptive Phase 2 Study In Sickle Cell Disease (GMIMarilyn J. DocID: 1ui8k - View Document
	I NEED TO KNOW ABOUT SICKLE CELL Transfusion Fact Sheet Volume 4, Number 16 By Carolyn Wilson What is sickle cell disease? Sickle cell disease is a condition which causes the body to make abnormal haemoglobin. Haemoglobi DocID: 1u7DQ - View Document
	Sickle cell disease and hyperhemolysis: epidemiology, risk factors and new therapeutic approaches in France WORLD APHERESIS ASSOCIATION AND FRENCH SOCIETY FOR HEMAPHERESIS April 27-29, 2016, PARIS-FRANCE DocID: 1sjCl - View Document
	S7 KHOEL Manual exchanges WAA DocID: 1rnBM - View Document