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Molecular and haematological characterisation of haemolytic anaemia associated with biallelic KLF1 mutations: a case series

Journal of clinical pathology, 2024-11, Vol.77 (11), p.783-789

2024

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Dominant β-thalassaemia with unusually high Hb A2 and Hb F caused by βCD121(−G) (HBB:c.364delG) in exon 3 of β-globin gene

Journal of clinical pathology, 2020-08, Vol.73 (8), p.511-513

2020

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Molecular basis of non-deletional HPFH in Thailand and identification of two novel mutations at the binding sites of CCAAT and GATA-1 transcription factors

Scientific reports, 2023-07, Vol.13 (1), p.11926-11926, Article 11926

2023

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δ-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia

Annals of hematology, 2021-08, Vol.100 (8), p.1953-1963

2021

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Factors associated with anaemia and iron deficiency among women of reproductive age in Northeast Thailand: a cross-sectional study

BMC public health, 2020-01, Vol.20 (1), p.102-102, Article 102

2020

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Molecular characterisation of haemoglobin E-Udon Thani (HBB:c.[79G>A;92+7A>G]): a novel form of Hb E-β-thalassaemia syndrome

Journal of clinical pathology, 2019-04, Vol.72 (4), p.322-324

2019

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Frequency of unnecessary prenatal diagnosis of hemoglobinopathies: A large retrospective analysis and implication to improvement of the control program

PloS one, 2023-04, Vol.18 (4), p.e0283051-e0283051

2023

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Loop-mediated isothermal amplification (LAMP) colorimetric phenol red assay for rapid identification of α0-thalassemia: Application to population screening and prenatal diagnosis

PloS one, 2022, Vol.17 (4), p.e0267832-e0267832

2022

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Molecular basis of Hb H and AEBart’s diseases in the Lao People’s Democratic Republic

International journal of laboratory hematology, 2020-02, Vol.42 (1), p.23-27

2020

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Hemoglobin EE disease in young Laotian children: Hematologic features and the contributions of genetic variations to Hb F expression

International journal of laboratory hematology, 2023-06, Vol.45 (3), p.387-393

2023

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A large cohort of hemoglobin variants in Thailand: molecular epidemiological study and diagnostic consideration

PloS one, 2014-09, Vol.9 (9), p.e108365-e108365

2014

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EE score: an index for simple differentiation of homozygous hemoglobin E and hemoglobin E-β0-thalassemia

Clinical chemistry and laboratory medicine, 2018-08, Vol.56 (9), p.1507

2018

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Generation of a single‐tube quality control material for hemoglobin and DNA analyses of hemoglobinopathies

International journal of laboratory hematology, 2022-06, Vol.44 (3), p.666-672

2022

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Anemia, iron deficiency, and thalassemia among the Thai population inhabiting at the Thailand-Lao PDR-Cambodia triangle

Scientific reports, 2022-11, Vol.12 (1), p.18643-18643, Article 18643

2022

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Erythrocyte indices in a large cohort of β‐thalassemia carrier: Implication for population screening in an area with high prevalence and heterogeneity of thalassemia

International journal of laboratory hematology, 2019-08, Vol.41 (4), p.513-518

2019

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Diagnostic value of fetal hemoglobin Bart's for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy

Orphanet journal of rare diseases, 2022-02, Vol.17 (1), p.45-45, Article 45

2022

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Results from 8 years of the proficiency testing program for diagnosis of hemoglobinopathies under the prevention and control program of thalassemia in Thailand

International journal of laboratory hematology, 2021-08, Vol.43 (4), p.845-852

2021

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A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders

Annals of hematology, 2020, Vol.99 (1), p.23-29

2020

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Anemia in an ethnic minority group in lower northern Thailand: A community-based study investigating the prevalence in relation to inherited hemoglobin disorders and iron deficiency

PloS one, 2023-06, Vol.18 (6), p.e0287527-e0287527

2023

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β‐Hemoglobinopathies in the Lao People's Democratic Republic: Molecular diagnostics and implication for a prevention and control program

International journal of laboratory hematology, 2021-06, Vol.43 (3), p.500-505

2021

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Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart’s disease: A hematological, molecular, and diagnostic aspects

International journal of laboratory hematology, 2020-08, Vol.42 (4), p.e173-e176

2020

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Molecular basis of a high Hb A2/Hb Fβ-thalassemia trait: a retrospective analysis, genotype-phenotype interaction, diagnostic implication, and identification of a novel interaction with α-globin gene triplication

PeerJ (San Francisco, CA), 2023-05, Vol.11, p.e15308-e15308

2023

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The Correlation Between Ineffective Erythropoiesis Biomarkers and Development of Extramedullary Hematopoiesis in Patients with Thalassemia

Mediterranean journal of hematology and infectious diseases, 2022-07, Vol.14 (1), p.e2022052-e2022052

2022

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Thalassemia and erythroid transcription factor KLF1 mutations associated with borderline hemoglobin A2 in the Thai population

Archives of medical science, 2022, Vol.18 (1), p.112-120

2022

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Hemoglobin Variants in Northern Thailand: Prevalence, Heterogeneity and Molecular Characteristics

Genetic testing and molecular biomarkers, 2016-01, Vol.20 (1), p.37-43

2016

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Molecular and haematological characterisation of haemolytic anaemia associated with biallelic KLF1 mutations: a case series

Dominant β-thalassaemia with unusually high Hb A2 and Hb F caused by βCD121(−G) (HBB:c.364delG) in exon 3 of β-globin gene

Molecular basis of non-deletional HPFH in Thailand and identification of two novel mutations at the binding sites of CCAAT and GATA-1 transcription factors

δ-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia

Factors associated with anaemia and iron deficiency among women of reproductive age in Northeast Thailand: a cross-sectional study

Molecular characterisation of haemoglobin E-Udon Thani (HBB:c.[79G>A;92+7A>G]): a novel form of Hb E-β-thalassaemia syndrome

Frequency of unnecessary prenatal diagnosis of hemoglobinopathies: A large retrospective analysis and implication to improvement of the control program

Loop-mediated isothermal amplification (LAMP) colorimetric phenol red assay for rapid identification of α0-thalassemia: Application to population screening and prenatal diagnosis

Molecular basis of Hb H and AEBart’s diseases in the Lao People’s Democratic Republic

Hemoglobin EE disease in young Laotian children: Hematologic features and the contributions of genetic variations to Hb F expression

A large cohort of hemoglobin variants in Thailand: molecular epidemiological study and diagnostic consideration

EE score: an index for simple differentiation of homozygous hemoglobin E and hemoglobin E-β0-thalassemia

Generation of a single‐tube quality control material for hemoglobin and DNA analyses of hemoglobinopathies

Anemia, iron deficiency, and thalassemia among the Thai population inhabiting at the Thailand-Lao PDR-Cambodia triangle

Erythrocyte indices in a large cohort of β‐thalassemia carrier: Implication for population screening in an area with high prevalence and heterogeneity of thalassemia

Diagnostic value of fetal hemoglobin Bart's for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy

Results from 8 years of the proficiency testing program for diagnosis of hemoglobinopathies under the prevention and control program of thalassemia in Thailand

A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders

Anemia in an ethnic minority group in lower northern Thailand: A community-based study investigating the prevalence in relation to inherited hemoglobin disorders and iron deficiency

β‐Hemoglobinopathies in the Lao People's Democratic Republic: Molecular diagnostics and implication for a prevention and control program

Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart’s disease: A hematological, molecular, and diagnostic aspects

Molecular basis of a high Hb A2/Hb Fβ-thalassemia trait: a retrospective analysis, genotype-phenotype interaction, diagnostic implication, and identification of a novel interaction with α-globin gene triplication

The Correlation Between Ineffective Erythropoiesis Biomarkers and Development of Extramedullary Hematopoiesis in Patients with Thalassemia

Thalassemia and erythroid transcription factor KLF1 mutations associated with borderline hemoglobin A2 in the Thai population

Hemoglobin Variants in Northern Thailand: Prevalence, Heterogeneity and Molecular Characteristics

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