Sitthichai Panyasai
Phayao, Thailand
Last Updated: 09/26/2026
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Found 48 publications
Preanalytical stability of hemoglobin H inclusion body detection using rapid brilliant cresyl blue staining: a genotype-stratified stability study in EDTA blood stored at 4 °C.
Journal: Laboratory medicine
Published: August 31, 2026
Identification of Clinically Relevant Hb Variants During HbA1c Testing Using the ARKRAY HA-8180V in Fast Mode: Reliable HbE Detection Based on Retention Time.
Journal: Annals of laboratory medicine
Published: April 02, 2026
Performance Evaluation of a Premier Resolution HPLC System for Detecting Hemoglobin Constant Spring, Hemoglobin Paksé, and Coexisting α- and β-Thalassemia Mutations.
Journal: Journal of clinical laboratory analysis
Published: September 29, 2025
Assessment of a High-Resolution HPLC System to Quantify HbE for α0-Thalassemia Diagnosis in HbE Heterozygotes.
Journal: Annals of laboratory medicine
Published: September 16, 2025
Complex interaction of δ-globin variant HbA2-Famagusta combined with β-globin variant Hb Monroe in cis with the HBB:c.-92C>G mutation: hematological characteristics and molecular diagnostic insights.
Journal: Expert review of hematology
Published: August 16, 2025
Genetic profiles and hematological characteristics of the α-Hb variant Hb Chumphae (HBA2:c.32T>A) in association with -SEA deletion α0-thalassemia.
Journal: Hematology, transfusion and cell therapy
Published: July 28, 2025
Molecular and hematological characteristics of two different δ-globin promoter variants, δ-276(A>G) and δ-77(T >C) among Thai, Burmese, and Laotian subjects.
Journal: PeerJ
Published: February 18, 2025
Interactions of electrophoretically silent hemoglobin Hekinan II [HBA1:c.84G>T] with various forms of α-thalassemias and other hemoglobinopathies: novel insights into the molecular and hematological characteristics and genetic origins.
Journal: The Libyan journal of medicine
Published: September 23, 2024
Novel Insights into Hb Shaare Zedek Associated with β0-Thalassemia: Molecular Characteristics, Genetic Origin and Diagnostic Approaches.
Journal: International journal of molecular sciences
Published: June 20, 2024
Unraveling thalassemia intermedia: Novel insights of a hemoglobin Jax [HBA2:c.44G>C] and deletional α0-thalassemia interaction phenotype.
Journal: Hematology, transfusion and cell therapy
Published: May 04, 2024
α-Globin mutations and Genetic Variants in γ-globin Promoters are Associated with Unelevated Hemoglobin F Expression of Atypical β0-thalassemia/HbE.
Journal: Archives of medical research
Published: December 13, 2023
Last Updated: 09/26/2026