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Single-tube multiplex real-time PCR with EvaGreen and high-resolution melting analysis for diagnosis of α0-thalassemia--SEA,--THAI, and--CR type deletions

PloS one, 2023-11, Vol.18 (11), p.e0293838-e0293838

2023

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Stability of control materials for α-thalassemia immunochromatographic strip test

Clinical chemistry and laboratory medicine, 2021-04, Vol.59 (5), p.e205-e207

2021

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Development of suitable external quality control material for G6PD deficiency screening with the fluorescent spot test

Clinical chemistry and laboratory medicine, 2020-01, Vol.58 (1), p.e18-e20

2020

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Lyophilized hemoglobin E control material for the dichlorophenol-indophenol (DCIP) test

Clinical chemistry and laboratory medicine, 2017-06, Vol.55 (6), p.e108-e109

2017

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Proficiency testing program for hemoglobin E, A2 and F analysis in Thailand using lyophilized hemoglobin control materials

Clinical chemistry and laboratory medicine, 2018-03, Vol.56 (4), p.602

2018

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Efficiency of lyophilized hemolysate control material in proficiency testing program for G6PD deficiency screening in Thailand

International journal of laboratory hematology, 2022-08, Vol.44 (4), p.e160-e163

2022

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Prevalences of SARS-CoV-2 RNA and anti-SARS-CoV-2 among at-risk populations in Chiang Mai and Lamphun provinces, Thailand, during November 2020-January 2021

PloS one, 2022-02, Vol.17 (2), p.e0263127-e0263127

2022

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Detection of the common South-East Asian β0-thalassemia mutations in samples with borderline HbA2 levels

Clinical chemistry and laboratory medicine, 2017-01, Vol.55 (1), p.e17

2017

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False-positive result of immunochromatographic (IC) strip test for the diagnosis of α-thalassemia in samples with autoantibodies

Clinical chemistry and laboratory medicine, 2020-01, Vol.58 (2), p.e44-e46

2020

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Development of molecular diagnostic platform for α0‐thalassemia 44.6 kb (Chiang Rai, ‐‐CR) deletion in individuals with microcytic red blood cells across Thailand

Annals of human genetics, 2023-05, Vol.87 (3), p.137-145

2023

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The FGFR1 Signaling Pathway Upregulates the Oncogenic Transcription Factor FOXQ1 to Promote Breast Cancer Cell Growth

International journal of biological sciences, 2023, Vol.19 (3), p.744-759

2023

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Diagnosis of Compound Heterozygous Hb Tak/β-Thalassemia and HbD-Punjab/β-Thalassemia by HbA2 Levels on Capillary Electrophoresis

Indian journal of hematology & blood transfusion, 2018, Vol.34 (1), p.110-114

2018

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Characterization and identification of Hb Bart’s hydrops fetalis caused by a compound heterozygous mutation ‐‐SEA/‐‐CR, a novel α0‐thalassemia deletion

International journal of laboratory hematology, 2020-06, Vol.42 (3), p.e116-e120

2020

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A Formula to Identify Potential Cases of β-Thalassemia/HbE Disease Among Patients With Absent HbA, HbE >75% and HbF Between 5 and 15

Laboratory medicine, 2019-04, Vol.50 (2), p.158-162

2019

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Hemoglobin Henri Mondor [β26(B8) Glu → Val, GAG > GTG], A First Case Report in South-East Asia

Indian journal of hematology & blood transfusion, 2020-01, Vol.36 (1), p.192-194

2020

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Uptake, acceptability and interpretability of 3-in-1 rapid blood self-testing for HIV, hepatitis B and hepatitis C

Journal of the International AIDS Society, 2022-12, Vol.25 (12), p.e26053-n/a

2022

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Serologic characteristics of hepatitis B virus among hill-tribe children in Omkoi district, Chiangmai province, Thailand

Journal of infection in developing countries, 2019-02, Vol.13 (2), p.169-173

2019

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Validation of Microarray for the Simultaneous Detection of Common α- and β-Thalassemia Gene Mutations

Laboratory medicine, 2019-07, Vol.50 (3), p.306-312

2019

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Hepatitis B prevalence and associated factors in adults presenting for infection screening in northern Thailand

Journal of Virus Eradication, 2023-12, Vol.9 (4), p.100356-100356, Article 100356

2023

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HbE Level and Red Cell Parameters in Heterozygous HbE With and Without α0-Thalassemia Trait

Indian journal of hematology & blood transfusion, 2018-10, Vol.34 (4), p.662-665

2018

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Control materials for immunochromatographic strip used for α-thalassemia screening

Clinical chemistry and laboratory medicine, 2016-04, Vol.54 (4), p.e113

Pornprasert, Sakorn

2016

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Thymic Function during 12 Months of Highly Active Antiretroviral Therapy in Thai HIV-Infected Patients with Normal and Slow Immune Recovery

Japanese Journal of Infectious Diseases, 2015, Vol.68(5), pp.353-356

2015

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Coinheritance of hemoglobin D-Punjab and β0-thalassemia 3.4 kb deletion in a Thai girl

Asian journal of transfusion science, 2017-01, Vol.11 (2), p.199-202

2017

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Preventive antiretroviral therapy in non-thalassemia carrier infants exposed to mother-to-child transmission of HIV decreases cord and after delivery red blood production without altering the development of hemoglobin

Current HIV research, 2014-01, Vol.12 (3), p.227-231

2014

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Association of Hb A2 Variants with Several Forms of α- and β-Thalassemia in Thailand

Hemoglobin, 2020-05, Vol.44 (3), p.179-183

2020

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Single-tube multiplex real-time PCR with EvaGreen and high-resolution melting analysis for diagnosis of α0-thalassemia--SEA,--THAI, and--CR type deletions

Stability of control materials for α-thalassemia immunochromatographic strip test

Development of suitable external quality control material for G6PD deficiency screening with the fluorescent spot test

Lyophilized hemoglobin E control material for the dichlorophenol-indophenol (DCIP) test

Proficiency testing program for hemoglobin E, A2 and F analysis in Thailand using lyophilized hemoglobin control materials

Efficiency of lyophilized hemolysate control material in proficiency testing program for G6PD deficiency screening in Thailand

Prevalences of SARS-CoV-2 RNA and anti-SARS-CoV-2 among at-risk populations in Chiang Mai and Lamphun provinces, Thailand, during November 2020-January 2021

Detection of the common South-East Asian β0-thalassemia mutations in samples with borderline HbA2 levels

False-positive result of immunochromatographic (IC) strip test for the diagnosis of α-thalassemia in samples with autoantibodies

Development of molecular diagnostic platform for α0‐thalassemia 44.6 kb (Chiang Rai, ‐‐CR) deletion in individuals with microcytic red blood cells across Thailand

The FGFR1 Signaling Pathway Upregulates the Oncogenic Transcription Factor FOXQ1 to Promote Breast Cancer Cell Growth

Diagnosis of Compound Heterozygous Hb Tak/β-Thalassemia and HbD-Punjab/β-Thalassemia by HbA2 Levels on Capillary Electrophoresis

Characterization and identification of Hb Bart’s hydrops fetalis caused by a compound heterozygous mutation ‐‐SEA/‐‐CR, a novel α0‐thalassemia deletion

A Formula to Identify Potential Cases of β-Thalassemia/HbE Disease Among Patients With Absent HbA, HbE >75% and HbF Between 5 and 15

Hemoglobin Henri Mondor [β26(B8) Glu → Val, GAG > GTG], A First Case Report in South-East Asia

Uptake, acceptability and interpretability of 3-in-1 rapid blood self-testing for HIV, hepatitis B and hepatitis C

Serologic characteristics of hepatitis B virus among hill-tribe children in Omkoi district, Chiangmai province, Thailand

Validation of Microarray for the Simultaneous Detection of Common α- and β-Thalassemia Gene Mutations

Hepatitis B prevalence and associated factors in adults presenting for infection screening in northern Thailand

HbE Level and Red Cell Parameters in Heterozygous HbE With and Without α0-Thalassemia Trait

Control materials for immunochromatographic strip used for α-thalassemia screening

Thymic Function during 12 Months of Highly Active Antiretroviral Therapy in Thai HIV-Infected Patients with Normal and Slow Immune Recovery

Coinheritance of hemoglobin D-Punjab and β0-thalassemia 3.4 kb deletion in a Thai girl

Preventive antiretroviral therapy in non-thalassemia carrier infants exposed to mother-to-child transmission of HIV decreases cord and after delivery red blood production without altering the development of hemoglobin

Association of Hb A2 Variants with Several Forms of α- and β-Thalassemia in Thailand

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