Sitthichai Panyasai

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

S. Panyasai, S. Satthakarn, N. Kunyanone, 2020, Scandinavian journal of clinical and laboratory investigation.

Interaction of hemoglobin E and several forms of alpha-thalassemia in Cambodian families.

J. Garcia-conde, A. Schmitt-Graeff, R. Paroni, 2003, Haematologica.

Molecular understanding of unusual HbE-β+-thalassemia with Hb phenotype similar to HbE heterozygote: simple and rapid differentiation using HbE levels

Wittaya Jomoui, S. Satthakarn, Sitthichai Panyasai, 2023, Annals of medicine.

Hematological Characterizations and Molecular Diagnostic Aspects of Hb Wiangpapao [α44(CE2)Pro→Ser (α1), CCG>TCG; HBA1: c.133C>T], a New α-Globin Variant Found in a Pregnant Thai Woman

S. Pornprasert, S. Panyasai, Sitthichai Panyasai, 2017, Hemoglobin.

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

S. Panyasai, Amphai Phasit, Sitthichai Panyasai, 2020, Hemoglobin.

Molecular basis and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in Thailand

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2004 .