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Diagnosis of common hemoglobinopathies among South East Asian population using capillary isoelectric focusing system

International journal of laboratory hematology, 2017-02, Vol.39 (1), p.101-111

2017

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Co‐inheritance of α0‐thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications

International journal of laboratory hematology, 2017-10, Vol.39 (5), p.508-512

2017

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Co-inheritance of α 0 -thalassemia elevates Hb A 2 level in homozygous Hb E: Diagnostic implications

International journal of laboratory hematology, 2017-10, Vol.39 (5), p.508-512

2017

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New updating into hemoglobinopathies

International journal of laboratory hematology, 2012-12, Vol.34 (6), p.559-565

2012

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Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system

International journal of laboratory hematology, 2011-08, Vol.33 (4), p.424-433

2011

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ICSH recommendations for the measurement of Haemoglobin A2

International journal of laboratory hematology, 2012-02, Vol.34 (1), p.1-13

2012

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Transplantation of Macaca cynomolgus iPS-derived hematopoietic cells in NSG immunodeficient mice

Haematologica (Roma), 2015-10, Vol.100 (10), p.e428-e431

2015

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ICSH recommendations for assessing automated high-performance liquid chromatography and capillary electrophoresis equipment for the quantitation of HbA2

International journal of laboratory hematology, 2015-10, Vol.37 (5), p.577-582

2015

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A reliable screening protocol for thalassemia and hemoglobinopathies in pregnancy: An alternative approach to electronic blood cell counting

American journal of clinical pathology, 2005, Vol.123 (1), p.113-118

2005

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Tandem measurements of iron and creatinine by cross injection analysis with application to urine from thalassemic patients

Talanta (Oxford), 2015-02, Vol.133, p.52-58

2015

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Genetic compound heterozygosity for Southeast Asian ovalocytosis and thalassemia in Thailand: prevalence and phenotypic analysis

Clinical genetics, 2014-02, Vol.85 (2), p.198-200

2014

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Red blood cell microparticles in hemoglobin E disorders

International journal of laboratory hematology, 2015-04, Vol.37 (2), p.e52-e55

2015

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ICSH recommendations for the measurement of Haemoglobin F

International journal of laboratory hematology, 2012-02, Vol.34 (1), p.14-20

2012

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Reversal of cardiac iron loading and dysfunction in thalassemic mice by curcuminoids

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2011-01, Vol.7 (1), p.62-69

2011

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Mitochondrial DNA polymorphisms in Thailand

Journal of human genetics, 2001-01, Vol.46 (3), p.115-125

2001

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Epigallocatechin-3-gallate and epicatechin-3-gallate from green tea decrease plasma non-transferrin bound iron and erythrocyte oxidative stress

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2007-05, Vol.3 (3), p.289-296

2007

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Curcumin contributes to in vitro removal of non-transferrin bound iron by deferiprone and desferrioxamine in thalassemic plasma

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2007-09, Vol.3 (5), p.469-474

2007

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Efficacy of curcuminoids in alleviation of iron overload and lipid peroxidation in thalassemic mice

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2009-09, Vol.5 (5), p.474-482

2009

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Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: A molecular and hematological analysis

Blood cells, molecules, & diseases, 2007-09, Vol.39 (2), p.195-198

2007

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Effects of green tea on iron accumulation and oxidative stress in livers of iron-challenged thalassemic mice

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2010-03, Vol.6 (2), p.57-64

2010

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Molecular characteristics of α+-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics

Clinical biochemistry, 2019-09, Vol.71 (C), p.31-37

2019

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Increase in non-transferrin bound iron and the oxidative stress status in epilepsy patients treated using valproic acid monotherapy

International journal of clinical pharmacology and therapeutics, 2011-04, Vol.49 (4), p.268-276

2011

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The hemoglobin E thalassemias

Cold Spring Harbor perspectives in medicine, 2012-08, Vol.2 (8), p.a011734-a011734

2012

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The Inherited Diseases of Haemoglobin Are an Emerging Global Health Burden

Thalassemia reports, 2011-12, Vol.1 (12), p.e1

2011

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β-Globin gene cluster polymorphisms are strongly associated with severity of HbE/β°-thalassemia

Clinical genetics, 2007-12, Vol.72 (6), p.497-505

2007

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Diagnosis of common hemoglobinopathies among South East Asian population using capillary isoelectric focusing system

Co‐inheritance of α0‐thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications

Co-inheritance of α 0 -thalassemia elevates Hb A 2 level in homozygous Hb E: Diagnostic implications

New updating into hemoglobinopathies

Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system

ICSH recommendations for the measurement of Haemoglobin A2

Transplantation of Macaca cynomolgus iPS-derived hematopoietic cells in NSG immunodeficient mice

ICSH recommendations for assessing automated high-performance liquid chromatography and capillary electrophoresis equipment for the quantitation of HbA2

A reliable screening protocol for thalassemia and hemoglobinopathies in pregnancy: An alternative approach to electronic blood cell counting

Tandem measurements of iron and creatinine by cross injection analysis with application to urine from thalassemic patients

Genetic compound heterozygosity for Southeast Asian ovalocytosis and thalassemia in Thailand: prevalence and phenotypic analysis

Red blood cell microparticles in hemoglobin E disorders

ICSH recommendations for the measurement of Haemoglobin F

Reversal of cardiac iron loading and dysfunction in thalassemic mice by curcuminoids

Mitochondrial DNA polymorphisms in Thailand

Epigallocatechin-3-gallate and epicatechin-3-gallate from green tea decrease plasma non-transferrin bound iron and erythrocyte oxidative stress

Curcumin contributes to in vitro removal of non-transferrin bound iron by deferiprone and desferrioxamine in thalassemic plasma

Efficacy of curcuminoids in alleviation of iron overload and lipid peroxidation in thalassemic mice

Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: A molecular and hematological analysis

Effects of green tea on iron accumulation and oxidative stress in livers of iron-challenged thalassemic mice

Molecular characteristics of α+-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics

Increase in non-transferrin bound iron and the oxidative stress status in epilepsy patients treated using valproic acid monotherapy

The hemoglobin E thalassemias

The Inherited Diseases of Haemoglobin Are an Emerging Global Health Burden

β-Globin gene cluster polymorphisms are strongly associated with severity of HbE/β°-thalassemia

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