Sitthichai Panyasai

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 12

Top Topics

Sickle Cell Disease

High Performance Liquid Chromatography

Top Venues

Scandinavian journal of clinical and laboratory investigation

Annals of medicine

International journal of molecular sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Surada Satthakarn, Wibhasiri Srisuwan, Naowarat Kunyanone, Sitthichai Panyasai
Novel Insights into Hb Shaare Zedek Associated with β 0 -Thalassemia: Molecular Characteristics, Genetic Origin and Diagnostic Approaches. International journal of molecular sciences 25 (16) (2024)
Surada Satthakarn, Wibhasiri Srisuwan, Naowarat Kunyanone, Sitthichai Panyasai
Novel Insights into Hb Shaare Zedek Associated with β 0 -Thalassemia: Molecular Characteristics, Genetic Origin and Diagnostic Approaches. International journal of molecular sciences 25 (16) (2024)
Sitthichai Panyasai, Kunyakan Khongthai, Surada Satthakarn
Hemoglobin profile and molecular characteristics of the complex interaction of hemoglobin Doi-Saket [α9(A7) asn > lys, HBA2:c.30C > a], a novel α2α1 hybrid globin variant, with hemoglobin E [β26(B8) Glu > lys, HBB:c.79G > A] and deletional α + -thalassemia in a Thai family. Annals of medicine 55 (2) (2023)
Wittaya Jomoui, Surada Satthakarn, Sitthichai Panyasai
Molecular understanding of unusual HbE-β + -thalassemia with Hb phenotype similar to HbE heterozygote: simple and rapid differentiation using HbE levels. Annals of medicine 55 (2) (2023)
Amphai Phasit, Sitthichai Panyasai, Monthon Mayoon, Niphawan Jettawan, Surada Satthakarn
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 13 (6) (2022)
Sitthichai Panyasai, Kanyakan Kongthai, Amphai Phasit
Association of Hb Shenyang [α26(B7)Ala→Glu, GCG>GAG, HBA2: c.80C>A (or HBA1)] with Several Types of α-Thalassemia in Thailand. Hemoglobin 44 (5) (2020)
Sitthichai Panyasai, Naowarat Kunyanone, Surada Satthakarn
Hb Athens-Georgia (beta 40(C6) Arg > Lys, HBB:c.122G > A) with a single α-globin gene (Hb H disease) in a Thai family: molecular, hematological, and diagnostic aspects. Scandinavian journal of clinical and laboratory investigation 81 (1) (2020)
Surada Satthakarn, Sasis Boonmee, Sitthichai Panyasai
Molecular Characterization and Hematological Aspects of Hb E-Myanmar [β26(B8)Glu→Lys and β65(E9)Lys→Asn, HBB: c.[79G>A;198G>C]): A Novel β-Thalassemic Hemoglobin Variant. Hemoglobin 44 (6) (2020)
Surada Satthakarn, Sitthichai Panyasai, Sakorn Pornprasert
Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A2 Levels. Hemoglobin 44 (5) (2020)
Sitthichai Panyasai, Sakorn Pornprasert
Association of Hb A2 Variants with Several Forms of α- and β-Thalassemia in Thailand. Hemoglobin 44 (3) (2020)
Wittaya Jomoui, Wanicha Tepakhan, Surada Satthakarn, Sitthichai Panyasai
Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in Thailand. Scandinavian journal of clinical and laboratory investigation 80 (7) (2020)
Sitthichai Panyasai, Amphai Phasit
α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (HBA1 or HBA2 c.96G>T or C)] with the α-Thalassemia-1 [- -SEA (Southeast Asian)] Deletion in Thailand. Hemoglobin 44 (4) (2020)