Molecular Characterization of Thalassemia intermedia Associated with HPFH-6/β-Thalassemia and HPFH-6/Hb E in Thai Patients

Publisher： Karger

E-ISSN： 1421-9662|108|3|157-161

ISSN： 0001-5792

Source： Acta Haematologica, Vol.108, Iss.3, 2002-09, pp. : 157-161

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Glomerular Hyperfiltration and Proteinuria in Transfusion-Independent Patients with β-Thalassemia Intermedia

By  

Nephron Clin Pract, Vol. 121, Iss. 3-4, 2012-12 ,pp. : c136-c143

Karger

Access to resources Recommend Favorite

Combination therapy with a Tmprss6RNAi‐therapeutic and the oral iron chelator deferiprone additively diminishes secondary iron overload in a mouse model of β‐thalassemia intermedia

By  

AMERICAN JOURNAL OF HEMATOLOGY, Vol. 90, Iss. 4, 2015-04 ,pp. : 310-313

John Wiley & Sons Inc

Access to resources Recommend Favorite

Mild Beta-Thalassemia intermedia Caused by Compound Heterozygosity for Gγ(Aγδβ)o/β-Thalassemia and Molecular Characterization of the Defect in Four Chinese Families

By  

Acta Haematologica, Vol. 109, Iss. 4, 2003-07 ,pp. : 169-175

Karger

Access to resources Recommend Favorite

Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia in Northeast Thailand

By  

Acta Haematologica, Vol. 136, Iss. 4, 2016-10 ,pp. : 233-239

Karger

Access to resources Recommend Favorite

Premature Atherosclerosis in Non-Transfusion-Dependent β-Thalassemia Intermedia

By  

Cardiology, Vol. 118, Iss. 3, 2011-06 ,pp. : 159-163

Karger

Access to resources Recommend Favorite