Molecular prevalence of thalassemia and hemoglobinopathies among the Lao Loum Group in the Lao People’s Democratic Republic

بواسطة Sayphonh Phanmany, Supantitra Chanprasert, Thongperm Munkongdee, Saovaros Svasti, Kamonlak Leecharoenkiat
منشور في 2020

Update in Laboratory Diagnosis of Thalassemia

بواسطة Thongperm Munkongdee, Ping Chen, Pranee Winichagoon, Suthat Fucharoen, Kittiphong Paiboonsukwong
منشور في 2020

Simple method for screening of α-thalassaemia 1 carriers

بواسطة Tayapiwatana C., Kuntaruk S., Tatu T., Chiampanichayakul S., Munkongdee T., Winichagoon P., Fuchareon S., Kasinrerk W.
منشور في 2014

Limit of sensitivity for melting curve screening for α-thalassemia

بواسطة Sriiam,S., Leecharoenkiat,A., Lithanatudom,P., Munkongdee,T., Svasti,S.L., Smith,D.R.
منشور في 2015

Coinheritance of the different copy numbers of α-globin gene modifies severity of β-thalassemia/Hb E disease

بواسطة Orapan Sripichai, Thongperm Munkongdee, Chutima Kumkhaek, Saovaros Svasti, Pranee Winichagoon, Suthat Fucharoen
منشور في 2018

Limit of sensitivity for melting curve screening for α-thalassemia

بواسطة Sukanya Sriiam, Amporn Leecharoenkiat, Pathrapol Lithanatudom, Thongperm Munkongdee, Saovaros Svasti, Duncan R. Smith
منشور في 2018

Genetic variation of Krüppel-like factor 1 (KLF1) and fetal hemoglobin (HbF) levels in β⁰-thalassemia/HbE disease

بواسطة Pinyaphat Khamphikham, Orapan Sripichai, Thongperm Munkongdee, Suthat Fucharoen, Sissades Tongsima, Duncan R. Smith
منشور في 2019

Molecular screening of the Hbs Constant Spring (codon 142, TAA>CAA, α2) and Paksé (codon 142, TAA>TAT, α2) mutations in Thailand

بواسطة Dalad Pichanun, Thongperm Munkongdee, Sumonmaln Klamchuen, Punnee Butthep, Pranee Winichagoon, Suthat Fucharoen, Saovaros Svasti
منشور في 2018

Rapid diagnosis of α-thalassemia by melting curve analysis

بواسطة Thongperm Munkongdee, Phantip Vattanaviboon, Parichut Thummarati, Paijit Sewamart, Pranee Winichagoon, Suthat Fucharoen, Saovaros Svasti
منشور في 2018

Molecular analysis of globin gene expression in different thalassaemia disorders: Individual variation of βE pre-mRNA splicing determine disease severity

بواسطة Alisa Tubsuwan, Thongperm Munkongdee, Natee Jearawiriyapaisarn, Chanikarn Boonchoy, Pranee Winichagoon, Suthat Fucharoen, Saovaros Svasti
منشور في 2018

Visual genotyping of thalassemia by using pyrrolidinyl peptide nucleic acid probes immobilized on carboxymethylcellulose-modified paper and enzyme-induced pigmentation

بواسطة Nuttapon Jirakittiwut, Thongperm Munkongdee, Kanet Wongravee, Orapan Sripichai, Suthat Fucharoen, Thanit Praneenararat, Tirayut Vilaivan
منشور في 2020

Simple method for screening of α-thalassaemia 1 carriers

بواسطة Chatchai Tayapiwatana, Surakit Kuntaruk, Thanusak Tatu, Sawitree Chiampanichayakul, Thongperm Munkongdee, Pranee Winichagoon, Suthat Fuchareon, Watchara Kasinrerk
منشور في 2018

Simple method for screening of α-thalassaemia 1 carriers

بواسطة Chatchai Tayapiwatana, Surakit Kuntaruk, Thanusak Tatu, Sawitree Chiampanichayakul, Thongperm Munkongdee, Pranee Winichagoon, Suthat Fuchareon, Watchara Kasinrerk
منشور في 2018

Maternal uniparental disomy of chromosome 16 resulting in hemoglobin Bart's hydrops fetalis

بواسطة Duangrurdee Wattanasirichaigoon, P. Promsonthi, A. Chuansumrit, J. Leopairut, P. Yanatatsaneejit, P. Rattanatanyong, T. Munkongdee, S. Fucharoen, A. Mutirangura
منشور في 2018

Simple method for screening of α-thalassaemia 1 carriers

بواسطة Chatchai Tayapiwatana, Surakit Kuntaruk, Thanusak Tatu, Sawitree Chiampanichayakul, Thongperm Munkongdee, Pranee Winichagoon, Suthat Fuchareon, Watchara Kasinrerk
منشور في 2018

Quantitative analysis of Hb Bart's in cord blood by capillary electrophoresis system

بواسطة Thongperm Munkongdee, Dalad Pichanun, Punnee Butthep, Sumonmaln Klamchuen, Veeradet Chalermpolprapa, Pranee Winichagoon, Saovaros Svasti, Suthat Fucharoen
منشور في 2018

A comprehensive ethnic-based analysis of alpha thalassaemia allelle frequency in northern Thailand article

بواسطة Kulaphisit M., Kampuansai J., Leecharoenkiat K., Wathikthinnakon M., Kangwanpong D., Munkongdee T., Svasti S., Fucharoen S., Smith D., Lithanatudom P.
منشور في 2017

Predictive SNPs for β⁰-thalassemia/HbE disease severity

بواسطة Thongperm Munkongdee, Sissades Tongsima, Chumpol Ngamphiw, Pongsakorn Wangkumhang, Chayanon Peerapittayamongkol, Hafizah Binti Hashim, Suthat Fucharoen, Saovaros Svasti
منشور في 2022

Association of SNP in exon 1 of HBS1L with hemoglobin F level in β⁰-thalassemia/hemoglobin e

بواسطة Riyaz A. Pandit, Saovaros Svasti, Orapan Sripichai, Thongperm Munkongdee, Kanokporn Triwitayakorn, Pranee Winichagoon, Suthat Fucharoen, Chayanon Peerapittayamongkol
منشور في 2018

Genetic analysis of candidate modifier polymorphisms in Hb E-β⁰-thalassemia patients

بواسطة Orapan Sripichai, Johanna Whitacre, Thongperm Munkongdee, Chutima Kumkhaek, Wattanan Makarasara, Pranee Winichagoon, Ken Abel, Andreas Braun, Suthat Fucharoen
منشور في 2018