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Hemoglobin H

An abnormal hemoglobin composed of four beta chains. It is caused by the reduced synthesis of the alpha chain. This abnormality results in ALPHA-THALASSEMIA.
Also Known As:
H, Hemoglobin
Networked: 78 relevant articles (0 outcomes, 3 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Taweevisit, Mana: 2 articles (05/2012 - 09/2010)
2. Vichinsky, Elliott P: 2 articles (02/2011 - 12/2005)
3. Olivieri, Nancy F: 2 articles (11/2009 - 12/2005)
4. Viprakasit, Vip: 2 articles (01/2009 - 02/2004)
5. Steensma, David P: 2 articles (11/2005 - 02/2004)
6. Halchuk, L: 1 article (10/2015)
7. Turley, E: 1 article (10/2015)
8. Verhovsek, M: 1 article (10/2015)
9. McFarlane, A: 1 article (10/2015)
10. Norasetthada, Lalita: 1 article (09/2015)

Related Diseases

1. alpha-Thalassemia
2. Anemia
3. Infection
4. Hemolysis
5. Thalassemia

Related Drugs and Biologics

1. DNA (Deoxyribonucleic Acid)
2. Hemoglobins (Hemoglobin)
3. Hemoglobin E
4. Brilliant Cresyl Blue
5. alpha-Globins
6. Iron
7. Hemoglobin A
8. Fetal Hemoglobin (Hemoglobin F)
9. Nonsense Codon (Nonsense Mutation)
10. Sulfhydryl Compounds (Thiols)

Related Therapies and Procedures

1. Splenectomy
2. Perioperative Period
3. Aftercare (After-Treatment)