Search Results - "Fucharoen, S"
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Diagnosis of common hemoglobinopathies among South East Asian population using capillary isoelectric focusing system
Published in International journal of laboratory hematology (01-02-2017)“…Summary Introduction We have evaluated an automated capillary isoelectric focusing (cIEF)‐based Hb analyzer in diagnosis of hemoglobinopathies commonly found…”
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New updating into hemoglobinopathies
Published in International journal of laboratory hematology (01-12-2012)“…Summary Thalassemia and abnormal hemoglobin are the most common genetic disorders and are considered health problems in many developing countries. In the last…”
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Co-inheritance of α 0 -thalassemia elevates Hb A 2 level in homozygous Hb E: Diagnostic implications
Published in International journal of laboratory hematology (01-10-2017)“…Differentiation of homozygous hemoglobin (Hb) E with and without α -thalassemia is subtle on routine hematological ground. We examined in a large cohort of…”
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Co‐inheritance of α0‐thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications
Published in International journal of laboratory hematology (01-10-2017)“…Introduction Differentiation of homozygous hemoglobin (Hb) E with and without α0‐thalassemia is subtle on routine hematological ground. We examined in a large…”
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Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system
Published in International journal of laboratory hematology (01-08-2011)“…Summary Introduction: This study was conducted to examine ability of the Capillarys 2 haemoglobin (Hb) testing system to assist in presumptive diagnosis of…”
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ICSH recommendations for the measurement of Haemoglobin A2
Published in International journal of laboratory hematology (01-02-2012)“…Summary Although DNA analysis is needed for characterization of the mutations that cause β‐thalassaemia, measurement of the Hb A2 is essential for the routine…”
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ICSH recommendations for assessing automated high-performance liquid chromatography and capillary electrophoresis equipment for the quantitation of HbA2
Published in International journal of laboratory hematology (01-10-2015)“…Summary Automated high performance liquid chromatography and Capillary electrophoresis are used to quantitate the proportion of Hemoglobin A2 (HbA2) in blood…”
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Tandem measurements of iron and creatinine by cross injection analysis with application to urine from thalassemic patients
Published in Talanta (Oxford) (01-02-2015)“…This work presents development of a method for the dual determination of Fe(III) and creatinine using cross injection analysis (CIA). Two CIA platforms…”
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Transplantation of Macaca cynomolgus iPS-derived hematopoietic cells in NSG immunodeficient mice
Published in Haematologica (Roma) (01-10-2015)Get full text
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ICSH recommendations for the measurement of Haemoglobin F
Published in International journal of laboratory hematology (01-02-2012)“…Summary Measurement of the Haemoglobin F in red cell haemolysates is important in the diagnosis of δβ thalassaemia, hereditary persistence of fetal haemoglobin…”
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Reversal of cardiac iron loading and dysfunction in thalassemic mice by curcuminoids
Published in Medicinal chemistry (Shp-sariqah, United Arab Emirates) (01-01-2011)“…Non-transferrin bound iron (NTBI) is found in plasma of β-thalassemia patients and causes oxidative tissue damage. Cardiac siderosis and complications are the…”
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Genetic compound heterozygosity for Southeast Asian ovalocytosis and thalassemia in Thailand: prevalence and phenotypic analysis
Published in Clinical genetics (01-02-2014)Get full text
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Red blood cell microparticles in hemoglobin E disorders
Published in International journal of laboratory hematology (01-04-2015)Get full text
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A reliable screening protocol for thalassemia and hemoglobinopathies in pregnancy: An alternative approach to electronic blood cell counting
Published in American journal of clinical pathology (2005)“…Primary screening for thalassemia and hemoglobinopathies usually involves an accurate blood count using an expensive electronic blood cell counter A cheaper…”
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Epigallocatechin-3-gallate and epicatechin-3-gallate from green tea decrease plasma non-transferrin bound iron and erythrocyte oxidative stress
Published in Medicinal chemistry (Shp-sariqah, United Arab Emirates) (01-05-2007)“…Beta-thalassemia patients suffer from secondary iron overload caused by increased iron absorption and multiple blood transfusions. Excessive iron catalyzes…”
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Curcumin contributes to in vitro removal of non-transferrin bound iron by deferiprone and desferrioxamine in thalassemic plasma
Published in Medicinal chemistry (Shp-sariqah, United Arab Emirates) (01-09-2007)“…Non-transferrin-bound iron (NTBI) is detectable in plasma of beta-thalassemia patients with transfusional iron overload. This form of iron may cause oxidative…”
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Efficacy of curcuminoids in alleviation of iron overload and lipid peroxidation in thalassemic mice
Published in Medicinal chemistry (Shp-sariqah, United Arab Emirates) (01-09-2009)“…Non-transferrin bound iron (NTBI) is detectable in plasma of beta-thalassemia patients and participates in free-radical formation and oxidative tissue damage…”
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Effects of green tea on iron accumulation and oxidative stress in livers of iron-challenged thalassemic mice
Published in Medicinal chemistry (Shp-sariqah, United Arab Emirates) (01-03-2010)“…Liver is affected by secondary iron overload in transfusions dependent b-thalassemia patients. The redox iron can generate reactive oxidants that damage…”
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Increase in non-transferrin bound iron and the oxidative stress status in epilepsy patients treated using valproic acid monotherapy
Published in International journal of clinical pharmacology and therapeutics (01-04-2011)“…This study aims to investigate the alteration of iron homeostasis and oxidative stress status in epilepsy patients treated with valproic acid (VPA)…”
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The Inherited Diseases of Haemoglobin Are an Emerging Global Health Burden
Published in Thalassemia reports (30-12-2011)“…Thalasseamia is one of the common genetic disorders. A genetic defect causes reduction of the globin chains leading to chronic haemolytic anaemia from birth…”
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