Two patients with α-chain hemoglobin variant Hb Q-Iran detected by measuring hemoglobin A1c using the variant mode of the HA-8180V HPLC analyzer

M Kinoshita, D Shimomura, M Shimada… - Diabetology …, 2024 - Springer
Hemoglobin variants are often discovered when hemoglobin A1c (HbA1c) levels measured
with a high-performance liquid chromatography (HPLC) system in fast mode are found to be …

First report of a Chinese family carrying a double heterozygosity for Hb Q-Thailand and Hb J-Bangkok

F Jiang, JY Zhou, JM Yan, YC Lu, DZ Li - Hemoglobin, 2016 - Taylor & Francis
The double heterozygosity for α and β chain variants leads to the formation of abnormal
heterodimer hybrids, which could render laboratory diagnostics in a routine setting difficult …

[PDF][PDF] Factors associated with hand, foot and mouth disease among children in Chiang Rai Province, northern Thailand: a hospital-based study

B Chaiwut, A Anuwatnonthakate… - Southeast Asian Journal …, 2019 - tm.mahidol.ac.th
Hand, foot and mouth disease (HFMD) is a common communicable disease that can result
in hospitalization. There is little information regarding the factors associated with HFMD …

Complex Interaction of Hb Q-Thailand (HBA1: c.223G>C) with β-Thalassemia/Hb E (HBB: c.79G>A) Disease

S Panyasai, S Satthakarn, S Pornprasert - Hemoglobin, 2018 - Taylor & Francis
Abstract Hb Q-Thailand [α74 (EF3) Asp→ His (α1), G AC> C AC, HBA1: c. 223G> C] is an
abnormal hemoglobin (Hb) frequently found in Thailand and Southeast Asian countries. The …

Complex Interaction of Hb Q-Thailand with α0- and β0-Thalassemia in a Chinese Family

S He, Q Qin, L Lin, Q Chen, S Yi, H Wei, J Du… - …, 2017 - Taylor & Francis
Abstract Hb Q-Thailand [α74 (EF3) Asp→ His (α1); HBA1: c. 223 G> C] is an abnormal
hemoglobin (Hb), variant found mainly in China and Southeast Asian countries. The …

Complex Interaction of Hb Q-Thailand with α and β Thalassemia in a Hakka Family

L Zheng, H Huang, X Wu, Q Shen, M Chen, M Wang… - 2020 - researchsquare.com
Background HbQ-Thailand is an α-globin chain variant that results from a point mutation at
codon 74 of the α1-globin gene on chromosome 16p. It commonly appears with a leftward …

[PDF][PDF] Complex Interaction of Hb Q-Thailand (HBA1: c. 223G> C) with β-Thalassemia/Hb E (HBB: c. 79G> A)

S Panyasai, S Satthakarn, S Pornprasert - researchgate.net
ABSTRACT Hb Q-Thailand [a74 (EF3) Asp! His (a1), GAC> CAC, HBA1: c. 223G> C] is an
abnormal hemoglobin (Hb) frequently found in Thailand and Southeast Asian countries. The …