Prevention and control of thalassemia in Asia

بواسطة Suthat Fucharoen, Pranee Winichagoon
منشور في 2010

Clinical and hematologic aspects of hemoglobin E β-thalassemia

بواسطة Suthat Fucharoen, Pranee Winichagoon
منشور في 2018

The molecular basis of thalassemias

بواسطة Suthat Fucharoen, Pranee Winichagoon
منشور في 2018

Hemoglobinopathies in Southeast Asia: Molecular Biology and Clinical Medicine

بواسطة Suthat Fucharoen, Pranee Winichagoon
منشور في 2018

Thalassemia and abnormal hemoglobin.

بواسطة Suthat Fucharoen, Pranee Winichagoon
منشور في 2018

Haemoglobinopathies in Southeast Asia

بواسطة Suthat Fucharoen, Pranee Winichagoon
منشور في 2018

Concomitant inheritance of α‐thalassemia in β°‐thalassemia/hb e disease

بواسطة Pranee Winichagoon, Suthat Fucharoen, David Weatherall, Prawase Wasi
منشور في 2018

Identification of HB lepore-mashington-Boston in association with HB e [βb26(b8)GLU→LYS] in a thai female

بواسطة Pratumtip Boontrakoonpoontawee, Jisnuson Svasti, Suthat Fucharoen, Pranee Winichagoon
منشور في 2018

Detection and haplotype differentiation of Southeast Asian α-thalassemia using polymerase chain reaction and a piezoelectric biosensor immobilized with a single oligonucleotide pro...

بواسطة Phantip Vattanaviboon, Kulphassorn Sangseekhiow, Pranee Winichagoon, Chamras Promptmas
منشور في 2018

Impaired Terminal Erythroid Maturation in β⁰-Thalassemia/HbE Patients with Different Clinical Severity

بواسطة Thunwarat Suriyun, Pranee Winichagoon, Suthat Fucharoen, Orapan Sripichai
منشور في 2022

Detection of α‐thalassemia‐1 (Southeast Asian type) and its application for prenatal diagnosis

بواسطة Pranee Winichagoon, Suthat Fucharoen, Sujin Kanokpongsakdi, Yazuyuki Fukumaki
منشور في 2018

Molecular mechanism of β-thalassaemia caused by 22-bp duplication

بواسطة Saovaros Svasti, Chanikarn Boonchoy, Preeda Vanichsetakul, Pranee Winichagoon, Suthat Fucharoen
منشور في 2018

Accelerated telomere shortening in β-thalassemia/HbE patients

بواسطة Pornthip Chaichompoo, Kovit Pattanapanyasat, Pranee Winichagoon, Suthat Fucharoen, Saovaros Svasti
منشور في 2018

Characterization of a novel deletion causing (δβ) ⁰-thalassemia in a Thai family

بواسطة Saovaros Svasti, Surachate Paksua, Issarang Nuchprayoon, Pranee Winichagoon, Suthat Fucharoen
منشور في 2018

β‐Thalassemia in Thailand

بواسطة PRANEE WINICHAGOON, SUTHAT FUCHAROEN, VARAPORN THONGLAIROAM, VEERAWAN TANAPOTIWIRUT, PRAWASE WASI
منشور في 2018

Hydroxyurea responses and fetal hemoglobin induction in β-thalassemia/HbE patients' peripheral blood erythroid cell culture

بواسطة Ramida Watanapokasin, Duangmanee Sanmund, Pranee Winichagoon, Koichiro Muta, Suthat Fucharoen
منشور في 2018

Molecular mechanism of high hemoglobin F production in Southeast Asian-type hereditary persistence of fetal hemoglobin

بواسطة Khaimuk Changsri, Varaporn Akkarapathumwong, Duangporn Jamsai, Pranee Winichagoon, Suthat Fucharoen
منشور في 2018

Discrimination of various thalassemia syndromes and iron deficiency and utilization of reticulocyte measurements in monitoring response to iron therapy

بواسطة Pranee Winichagoon, Rawiprapa Kumbunlue, Pornpan Sirankapracha, Piathip Boonmongkol, Suthat Fucharoen
منشور في 2018

Detection of ζ-globin chains in the cord blood by ELISA (Enzyme-Linked Immunosorbent Assay): Rapid screening for α-thalassemia 1 (Southeast Asian Type)

بواسطة Ruchanee Ausavarungnirun, Pranee Winichagoon, Suthat Fucharoen, Nava Epstein, Ronald Simkins
منشور في 2018

Two cases of compound heterozygosity for Hb Hekinan [α27(B8)Glu→ Asp (α1)] and α-thalassemia in Thailand

بواسطة Lukana Ngiwsara, Chantragan Srisomsap, Pranee Winichagoon, Suthat Fucharoen, Jisnuson Svasti
منشور في 2018