Thalassemia and related RBC disorders

Panyasai S, Kunyanone N, Satthakarn S. Hb Athens-Georgia (40(C6) Arg > Lys, HBB:c.122G > A) with a single -globin gene (Hb H disease) in a Thai family: molecular, hematological, and diagnostic aspects. Scand J Clin Lab Invest. 2021 Feb;81(1):52-58.

Prajantasen T, Prayalaw P, Panyasai S, Binlee S, Nongnuan S. Development of a High Resolution Melting Curve Analysis for the Detection of Hemoglobin δ-Chain Variants in Thailand and Identification of Hb A2-Walsgrave [codon 52 (GAT>CAT), Asp→His; HBD:c.157G>C] in a Pregnant Woman from Southern Thailand. Genet Test Mol Biomarkers. 2021;25(6):426-433.

Phasit A, Panyasai S, Mayoon M, Jettawan N, Satthakarn S. Phenotypic Expression of Known and Novel Hemoglobin A2-Variants, Hemoglobin A2-Mae Phrik [Delta 52(D3) Asp > Gly, HBD:c.158A > G], Associated with Hemoglobin E [Beta 26(B8) Glu > Lys, HBB:c.79G > A] in Thailand. Genes (Basel). 2022;13(6):959. Published 2022 May 27. doi:10.3390/genes13060959.

Satthakarn S, Panyasai K, Phasit A, Panyasai S. Reliability of hemoglobin A2 value as measured by the Premier Resolution system for screening of b-thalassemia carriers. Clin Chem Lab Med. 2023 Oct 17;62(3):453-463.

Jomoui W, Satthakarn S, Panyasai S. Molecular understanding of unusual HbE-b+-thalassemia with Hb phenotype similar to HbE heterozygote: simple and rapid differentiation using HbE levels. Ann Med. 2023;55(2):2267054.

Panyasai S, Khongthai K, Satthakarn S. Hemoglobin profile and molecular characteristics of the complex interaction of hemoglobin Doi-Saket [a9(A7) asn > lys, HBA2:c.30C > a], a novel a2a1 hybrid globin variant, with hemoglobin E [b26(B8) Glu > lys, HBB:c.79G > A] and deletional a+-thalassemia in a Thai family. Ann Med. 2023;55(2):2264174.

Panyasai S, Satthakarn S, Phasit A. Effective screening of hemoglobin Constant Spring and hemoglobin Paksé with several forms of a- and b-thalassemia in an area with a high prevalence and heterogeneity of thalassemia using capillary electrophoresis. Heliyon. 2023 Aug 12;9(8):e19116.

Jomoui W, Panyasai S, Sripornsawan P, Tepakhan W. Revisiting and updating molecular epidemiology of a-thalassemia mutations in Thailand using MLPA and new multiplex gap-PCR for nine a-thalassemia deletion. Sci Rep. 2023;13(1):9850.

Panyasai S, Chantanaskulwong P, Permsripong N, Mokmued T. Interactions of electrophoretically silent hemoglobin Hekinan II [HBA1:c.84G>T] with various forms of a-thalassemias and other hemoglobinopathies: novel insights into the molecular and hematological characteristics and genetic origins. Libyan J Med. 2024 Dec 31;19(1):2406620.

Satthakarn S, Srisuwan W, Kunyanone N, Panyasai S. Novel Insights into Hb Shaare Zedek Associated with b0-Thalassemia: Molecular Characteristics, Genetic Origin and Diagnostic Approaches. Int J Mol Sci. 2024 Aug 6;25(16):8578.

Satthakarn S, Panyasai S. a-Globin mutations and Genetic Variants in g-globin Promoters are Associated with Unelevated Hemoglobin F Expression of Atypical b0-thalassemia/HbE. Arch Med Res. 2024 Sep;55(6):103055.

Panyasai S, Jaiping K, Khantarag P, Nochod P, Satthakarn S. Unraveling thalassemia intermedia: Novel insights of a hemoglobin Jax [HBA2:c.44G>C] and deletional a0-thalassemia interaction phenotype. Hematol Transfus Cell Ther. 2025 Jan-Mar;47(1):103739.

Panyasai S, Srisuwan W, Sumphanapai T, Satthakarn S. Complex interaction of d-globin variant HbA2-Famagusta combined with b-globin variant Hb Monroe in cis with the HBB:c.-92C>G mutation: hematological characteristics and molecular diagnostic insights. Expert Rev Hematol. 2025 Aug 25:1-15. doi: 10.1080/17474086.2025.2549379