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Literature DB >> 9255610

Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine.

S Fucharoen¹, P Winichagoon.

Abstract

Entities: Disease

Mesh：

Year: 1997 PMID： 9255610 DOI： 10.3109/03630269709000664

Source DB: PubMed Journal: Hemoglobin ISSN： 0363-0269 Impact factor: 0.849

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21 in total

1. Screening for co-existence of α-thalassemia in β-thalassemia and in HbE heterozygotes via an enzyme-linked immunosorbent assay for Hb Bart's and embryonic ζ-globin chain.

Authors: Thanusak Tatu; Tiemjan Kiewkarnkha; Surakit Khuntarak; Sakdinan Khamrin; Surasit Suwannasin; Watchara Kasinrerk
Journal: Int J Hematol Date: 2012-03-23 Impact factor: 2.490

2. A mechanism of ineffective erythropoiesis in β-thalassemia/Hb E disease.

Authors: Pathrapol Lithanatudom; Amporn Leecharoenkiat; Tirawat Wannatung; Saovaros Svasti; Suthat Fucharoen; Duncan R Smith
Journal: Haematologica Date: 2009-12-16 Impact factor: 9.941

3. Rapid diagnosis of alpha-thalassemia by melting curve analysis.

Authors: Thongperm Munkongdee; Phantip Vattanaviboon; Parichut Thummarati; Paijit Sewamart; Pranee Winichagoon; Suthat Fucharoen; Saovaros Svasti
Journal: J Mol Diagn Date: 2010-02-26 Impact factor: 5.568

4. Effect of Swiss-type heterocellular HPFH from XmnI-Gγ and HBBP1 polymorphisms on HbF, HbE, MCV and MCH levels in Thai HbE carriers.

Authors: Sasiwan Kerdpoo; Ektong Limweeraprajak; Thanusak Tatu
Journal: Int J Hematol Date: 2014-01-29 Impact factor: 2.490

Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine.

1. Screening for co-existence of α-thalassemia in β-thalassemia and in HbE heterozygotes via an enzyme-linked immunosorbent assay for Hb Bart's and embryonic ζ-globin chain.

2. A mechanism of ineffective erythropoiesis in β-thalassemia/Hb E disease.

3. Rapid diagnosis of alpha-thalassemia by melting curve analysis.

4. Effect of Swiss-type heterocellular HPFH from XmnI-Gγ and HBBP1 polymorphisms on HbF, HbE, MCV and MCH levels in Thai HbE carriers.

Review 5. Beta-thalassemia in the Korean population.

Review 6. The inherited diseases of hemoglobin are an emerging global health burden.

Review 7. Iron chelation therapy in the management of thalassemia: the Asian perspectives.

8. Renal tubule function in beta-thalassemia after hematopoietic stem cell transplantation.

9. Interaction of malaria with a common form of severe thalassemia in an Asian population.

10. Sandwich ELISA for hemoglobin A2 quantification and identification of beta-thalassemia carriers.