Publications ของโครงการฯ (1984-2007)

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Publications

Non-transferrin plasma iron in ß-thalassaemia/Hb E and haemoglobin H diseases.[Article]
Anemia in tropical and geographical medicine.[Article]
Cholecystitis associated with Enterobacter agglomerans. [Article]
The molecular basis of alpha-thalassaemia in Thailand. [Article]
Hematologic and biosynthetic studies in homozygous hemoglobin Constant Spring. [Article]
Determination for different severity of anemia in thalassemia: concordance and discordance among sib pairs.[Article]
Increased red blood cell protoporphyrin in thalassemia: a result of relative iron deficiency. [Article]
Ultrastructure and cell cycle distribution of erythropoietic cells in heterozygotes and homozygotes for haemoglobin E. [Article]
Cardiac pathology in 47 patients with beta- thalassemia/hemoglobin E. [Article]
Improved technic for detecting intraerythrocytic inclusion bodies in alpha-thalassemia trait.[Acticle]
Intracranial extramedullary hematopoiesis inducing epilepsy in a patient with beta-thalassemia- hemoglobin E.[Article]
Quantitative changes of red blood cell shapes in relation to clinical features in beta-thalassemia/Hb E disease.[Article]
Thalassemia in Southeast Asia: determination of different degrees of severity of anemia in thalassemia. [Article]
Vitamin E in beta-thalassaemia and alpha-thalassaemia (Hb H) diseases.[Article]
Concomitant inheritance of alpha-thalassemia in beta⁰-thalassemia/Hb E disease.[Article]
Prevalence of HTLV-III/LAV antibody in selected populations in Thailand.
[Article]
The morphology of redox-dye-treated Hb H-containing red cells: differences between cells treated with brilliant cresyl blue, methylene blue and new methylene blue. [Article]
Molecular mechanisms of thalassemia in Thailand. [Article]
Iron deficiency anemia.[Article]
The relation of erythropoiesis to iron absorption in thalassemia. [Article]
Iron overload in Hb E-beta-thalassemia : magnetic measurement of hepatic iron stores. [Article]
Hb H disease: iron overload is more severe in the genotype alpha-thalassemia-1/Hb Constant Spring than in alpha-thalassemia-1/alpha-thalassemia 2.
[Article]
Studies of erythropoietic cells in heterozygotes and homozygotes for haemoglobin Constant Spring and in heterozygotes for both haemoglobin Constant Spring and beta-thalassaemia 1 trait : extent of globin chain precipitation and cell cycle distribution.[Article]
The Problems of thalassaemia in South-East Asia. In : National Congress in Hematology and Transfusion, Soemantri Ag and Pradono AP. (eds.). [Article]
Increased phagocytosis of plasmodium falciparum-infected erythrocytes with haemoglobin E by peripheral blood monocytes.[Article]
Comparison of erythrocyte antioxidative enzyme activities between two types of haemoglobin H disease.[Article]
Geographic distribution of hemoglobin variants in Southeast Asia. In: Hemoglobin Variants in Human Populations Vol II, Winter WP. (ed.). CRC Press Inc.,[Article]
Free oxygen radicals and free oxygen radicals scavenging enzymes in thalassemia. [Article]
Erythroid marrow function in anemic patients. [Article]
Failure to detect large deletions in the beta-globin gene of Thai subjects with beta^o-thalassemia/Hb E.[Article]
Prenatal diagnosis of the fetus at risk for beta-thalassemia/ hemoglobin E disease: a report of the first case in Thailand.[Article]
Thalassemic erythrocytes inhibit in vitro growth of plasmodium falciparum.[Article]
Iron chelating agents. [Article]
Hemoglobinopathies in Southeast Asia.[Article]
Defective spectrin dimer self-association in thalassemic red cells. [Article]
Identification of Hb Lapore-Washington-Boston in association with Hb E [b26(B8)Glu->Lys] in a Thai Female. [Article]
Different severity of homozygous beta- thalassemia among siblings. [Article]
Different molecular defects of ^Gg(^Agdb)^o-thalassaemia in Thailand. [Article]
Inhibitory effect of beta^o-thalassaemia/haemoglobin E erythrocytes on plasmodium falciparum growth in vitro.[Article]
Adequacy of iron supply for erythropoiesis: In vivo observations in humans.[Article]
Plasma iron and transferrin iron-binding capacity evaluated by colorimetric and immunoprecipitation methods. [Article]
A mild uncompensated alkalosis in anemia. [Atricle]
Decreased heat stability found in purified hemoglobin Queens [alpha34(B15)Leu->Arg]. [Article]
Impaired glucose counterregulation after insulin induced hypoglycemia in thalassemia patients [Article]
Studies of hemoglobin Bart’s and deletion of alpha-globin genes from cord blood in Thailand. [Article]
alpha-mRNA level in the two types of Hb H disease. [Article]
Molecular basis of beta-thalassemia in Thailand. [Article]
Bam HI polymorphism of the betaA–,betaE–, and beta^o-thalassemia genes in the Thai population.[Article]
DNA polymorphism of betaN- and betaE-globin genes in Thais. [Article]
Altered structure of spectrin in the two types of hemoglobin H disease.[Article]
A scanning electron microscopic study of red cells of thalassemic patients. [Article]
Red cell osmotic fragility by fragiligraphic study in normal, thalassemic, and hemoglobin E patients. [Article]
Oxidative stress and antioxidative enzymes in hemoglobin H disease. [Article]
Oxidative stress and antioxidants in beta-thalassemia/hemoglobin E. [Article]
elationship of serum vitamin E, erythrocyte nonheme iron, and malonyldialdehyde ( lipid membrane peroxidation product) in thalassemia.[Article]
Modified technique for detecting red cells containing inclusion bodies in alpha-thalassemia trait.[Article]
Effects of toluene and storage on the amount of Hb H. [Article]
No evidence for a role of disulfide bonds in the attachment of inclusion bodies of the red cell membrane.[Article]
Variable severity of Southeast Asian beta^o-thalassemia/Hb E disease.
[Article]
Determination of variable severity of anemia in thalassemia : erythrocyte proteolytic activity. [Article]
Differential expression of erythrocyte calpain and calpastatin activities in beta^o-thalassemia/Hb E disease. [Article]
Double heterozygosity for hemoglobin E and a Lepore-type hemoglobin found in a Thai woman. [Article]
Differences between two types of Hb H disease, alpha-thalassemia 1/alpha thalassemia 2 and alpha-thalassemia 1/Hb Constant Spring.
[Article]
In vivo induction of intraerythrocytic inclusion bodies in hemoglobin H disease : an electron microscopic study.[Article]
Clinical and hematologic manifestations of AE Bart’s disease. [Article]
Hemoglobin Bart’s disease without hydrops manifestation. [Article]
Lung function tests in splenectomized beta-thalassemia/Hb E patients. [Article]
Lung perfusion in thalassemia. [Article]
Distribution of pulmonary thromboembolic lesions in thalassemic patients. [Article]
Patients with thalassemia develop osteoporosis, osteomalacia, and hypoparathyroidism, all of which are corrected by transfusion.[Article]
Deaths in beta-thalassemia/Hb E patients secondary to infections.[Article]
Infection in thalassemia: a retrospective study of 1,018 patients with beta-thalassemia/Hb E disease. [Article]
A study of infective episodes in patients with b-thalassemia/Hb E disease in Thailand. [Article]
Severe infection in thalassemia: a prospective study.[Article]
Antibody response in beta-thalassemia/Hb E disease, hemoglobin H patients, and nonthalassemics with enteric fever.[Article]
Oropharyngeal colonization with aerobic bacteria in beta-thalassemia/ hemoglobin E disease.[Article]
Serum of thalassemic patients promotes growth of streptococci. [Article]
Viral infections in beta-thalassemia/hemoglobin E patients. [Article]
Iron metabolism in thalassemia.[Article]
Histochemical study of liver tissue from thalassemic patients. [Article]
Electron microscopic study of liver tissue from 30 thalassemic patients. [Article]
Plasma renin activity in patients with beta-thalassemia hemoglobin E. [Article]
Gallstones in thalassemia.[Article]
Cholecystectomy in thalassemia. [Article]
A study of thalassemia associated with pregnancy.[Article]
Study of hematopoietic progenitors in patients with thalassemia: the effect of splenectomy.[Article]
Investigation of the causes of suboptimal haemoglobin response to iron supplementation.[Article]
The effect of erythroid hyperplasia on iron balance. [Article]
Cord blood study on beta-thalassemia and hemoglobin E. [Article]
EF Bart’s disease: Interaction of the abnormal a-and beta-globin genes.[Article]
Assessment of hematological data obtained by the aperture impedance method in blood from patients with thalassemia or hemoglobinopathy. [Article]
Problems of thalassemia in Thailand. [Article]
Pathophysiology of thalassemic erythrocytes. [Article]
Infections in thalassemia. [Article]
A WHO collaborative study on iron supplementation in Burma and in Thailand.
[Article]
Prevention of a-thalassemia. In : Prenatal diagnosis of thalassemia and the hemoglobinopathies, Loukopoulos D (ed.).[Article]
Quantitation of ferritin iron in plasma, an explanation for non-transferrin iron.
[Article]
A historical challenge to medical education (Editorial).[Article]
Impaired parasite growth and increased susceptibility to phagocytosis of plasmodium falciparum infected alpha-thalassemia or hemoglobin Constant Spring red blood cells. [Article]
Hematologic changes in a-thalassemia. [Article]
alpha-thalassemia in Thailand. [Article]
beta-Thalassemia associated with alpha-thalassemia in Thailand. [Article]
Characterization of two deletions that remove the entire human z-a globin gene complex (–THAI and –FIL). [Article]
Analysis of hematological data of thalassemia cases in Thailand. [Article]
Effects of thalassemic serum on the in vitro development of the malarial parasite plasmodium falciparum. [Article]
Decreased sensitivity to artesunate and chloroquine of plasmodium falciparum infecting hemoglobin H and/or hemoglobin Constant Spring erythrocytes. [Article]
The molecular basis of AE-Bart’s disease. [Article]
A novel ochre mutation in the beta-thalassemia gene of a Thai. [Article]
Detection of beta-thalassemia and hemoglobin E genes in Thai by a DNA amplification technique.[Article]
Molecular basis of bo-thalassemia/Hb E disease in Thailand. [Article]
Selective enzymatic amplification of a2-globin DNA for detection of the hemoglobin Constant Spring mutation.[Article]
Laboratory diagnosis for thalassemia. [Article]
Study of mechanisms of post-transfusion hypertension in thalassaemic patients. [Article]
The molecular basis of thalassemias. [Article]
Cytochemical evaluation of neutrophil components in beta-thalassemia hemoglobin E. [Article]
The role of humoral factor causing post-transfusion hypertension in thalassemic patients. [Article]
Intact transferrin receptors in human plasma and their relation to erythropoiesis.[Article]
Effect of thalassemia/ hemoglobin E disease on macro, trace, and ultratrace element concentrations in human tissue. [Article]
Prenatal diagnosis of beta(^o)-thalassemia/hemoglobin E disease by DNA amplification technique. [Article]
Electron microscopical and immumohistochemical studies of liver tissue in thalassaemic patients emphasis of iron and hepatitis B virus.[Article]
Cardiac involvement in beta-thalassemia/hemoglobin E disease: clinical and hemodynamic findings.[Article]
Thai Gg(Agdb)o-thalassemia and its interaction with a single g-globin gene on a chromosome carrying bo-thalassemia. [Article]
Haemoglobin-E trait and the clinical course of malaria in Thai soldiers. [Article]
The molecular basis of beta-thalassemia in Thailand: application to prenatal diagnosis.[Article]
Hemoglobin Dhonburi a2b2 126(H4) Val->Gly: a new unstable b variant producing a beta-thalassemia intermedia phenotype in association with beta^o-thalassemia. [Article]
Control of thalassaemia in Southeast Asia. [Article]
Induction of zoopore formation in Thai isolates of Pythium insidiosum. [Article]
Ultrasonographic method for detection of haemoglobin Bart’s hydrops fetalis in the second trimester of pregnancy. [Article]
beta-thalassaemia/ haemoglobin E tissue ferritins. I: purification and partial characterization of liver and spleen ferritins. [Article]
beta-thalassaimia/haemoglobin E tissue ferritins. II: a comparison of heart and pancreas ferritins with those of liver and spleen. [Article]
The interference of pyridoxal isonicotinoyl hydrazone with intestinal iron absorption. [Article]
beta-thalassemia in Thailand. [Article]
Pituitary function in thalassemic patients and the effect of chelation therapy.
[Article]
Organ specific crystalline structures of ferritin cores in beta-thalassemia/hemoglobin E..[Article]
Prenatal diagnosis of thalassemia and hemoglobinopathies in Thailand: experience from 100 pregnancies. [Article]
Mineralization of iron in ferritin and haemosiderin: the effect of tissue environment on mineral structure. Machanisms and phylogeny of mineralization in biological system, Suga S and Nakahara H (eds) Springer-Verlag,[Article]
Red cell and plasma calcium, copper and zinc in beta-thalassemia/hemoglobin E.[Article]
Asymmetrically primed selective amplification/temperature shift fluorescence polymerase chain reaction to detect the hemoglobin Constant Spring mutation. [Article]
High-dose intravenous immunoglobulin in the management of immune hemolysis in patients with thalassemic disease: factors which determine refractoriness.[Article]
Erythroblast and erythrocyte-bound antibodies in a and b thalassemia syndromes. [Article]
Hemoglobin Constant Spring in Bangkok: molecular screening by selective enzymatic amplification of the a2 globin gene. [Article]
Erythrocyte volume and haemoglobin concentration in haemoglobin H Disease: discrimination between the two genotypes.[Article]
Erythrocyte glocose-6-phosphate dehydrogenase and pyruvate kinase activities in hemoglobin H Disease. [Article]
duced deformability of thalassemic erythrocytes and erythrocytes with abnormal hemoglobins and relation with susceptibility of Plasmodium falciparum invasion.[Article]
Identification of five rare mutations including a novel frameshift mutation causing bo-thalassemia in Thai patients with bo-thalassemia/hemoglobin E disease.[Article]
Core structures of haemosiderins deposited in varions organs in beta-thalassaemia/haemoglobin E disease. [Article]
Effect of orally active hydroxypyridinone iron chelators on human lymphocyte function. [Article]
Flow cytometric two-color staining technique for simultaneous determination of human erythrocyte membrane antigen and intracellular malarial DNA. [Article]
Thalassemia in Southeast Asia: problems and strategy for prevention and control.
[Article]
Hb Q Thailand [a74 (EF3) Asp->His]: gene organization, molecular structure, and DNA diagnosis. [Article]
Cytoadherence characteristics of rosette-forming plasmodium falciparum. [Article]
Flow cytometry and its application on malaria.[Article]
The molecular basis of alpha-thalassemia in Thailand. [Article]
Molecular heterogeneity of beta-thalassemia in Thailand. [Article]
Hypoxemia in thalassemia. [Article]
Pulmonary thromboembolism in thalassemic patients. [Article]
The pathogenesis of hypoxemia.[Article]
Increase in spontaneous platelet aggregation in beta-thalassemia/hemoglobin E disease: a consequence of splenectomy.[Article]
Detection of PF3 availability in whole blood from volunteers and beta-thalassemia/HbE patients: a promissing method for prediction of thrombolytic tendency. [Article]
Morphological assessment of platelet activation in thalassemia.[Article]
Protein C and protein S deficiency in thalassemic patients. [Article]
The thalassemic red cell membrane. [Article]
Size distribution curves of blood cells in thalassemias and hemoglobin H diseases. [Article]
Biophysical changes of red cells with thalassemia-like abnormal hemoglobin.
[Article]
Interaction between endothelial cells and thalassemic red cells in vitro. [Article]
Thalassemic serum impairs endothelial cell growth in vitro.[Article]
Liver tissue injury secondary to iron overload in beta-thalassemia/hemoglobin E disease. [Article]
Brain pathology in 6 fatal cases of post-transfusion hypertension, convulsion and cerebral hemorrhage syndrome. [Article]
wo-color flow cytometric analysis of intraerythrocytic malaria parasite DNA and surface membrane-associated antigen in erythrocytes infected with plasmodium falciparum. [Article]
Severity differences in beta-thalassemia/haemoglobin E syndromes: implication of genetic factor.[Article]
Fatal arteritis due to Pythium insidiosum infection in patients with thalassemia. [Article]
Identification of Hb C [B6(A3)Glu->Lys] in a Thai Male. [Article]
Alteration in cytoadherence and rosetting of plasmodium falciparum-infected thalassemic red blood cells.[Article]
Activation of monocytes for the immune clearance of red cells in beta^o-thalassemia/HbE. [Article]
Quantitative assessment of erythropoiesis and functional classification of anemia based on measurements of serum transferrin receptor and erythropoietin.[Article]
Identification of Hb Anantharaj [all (A9)LYS->GLU] as Hb J-Wenchang-Wuming [all (A9)LYS->GLU]. [Article]
Structural analysis of proteins in Thailand : Identification of abnormal hemoglobins. [Article]
Structure of Abnormal Hemoglobins in Thailand. “Recent Advances in Molecular and Biochemical Research on Proteins”. [Article]
Effect of pyrexia in the formation of intraerythrocytic inclusion bodies and vacuoles in haemolytic crisis of haemoglobin H disease.[Article]
Nondeletional type of hereditary persistence of fetal haemoglbin: molecular characterization of three unrelated Thai HPFH. [Article]
Monoclonal antibody immunoassay for the identification of hemoglobin variants in neonatal screening. [Article]
Hydration of red cells in a and beta thalassemia differs a useful approach to distinguish between these red cell phenotypes. [Article]
Number and maturation of reticulocytes in various genotypes of thalassemia as assessed by flow cytometry.[Article]
Flow cytometric immunophenotyping of lymphocyte subsets in samples that contain a high proportion of non-lymphoid cells. [Article]
The ethics of prenatal diagnosis in different religious and cultural contexts. In Beuzard Y, Lubin B, Rosa J (eds). Sinckle Cell Disease and Thalassaemia: New Trends in Therapy. [Article]
Hydroxyurea increases Hb F and improves the effectiveness of erythropoiesis in beta-thalassemia/Hb E disease. In Beuzard Y, Lubin B, Rosa J (eds). Sinckle Cell Disease and Thalassaemia: New Trends in Therapy. [Article]
Detection of alpha-thalassemia-1 (Southeast Asian type) and its application for prenatal diagnosis. [Article]
Reverse dot-blot detection of Thai beta-thalassaemia mutations. [Article]
Alterations in vascular endothelial cell-related plasma proteins in thalassaemic patients and their correlation with clinical symptoms. [Article]
Molecular mechanisms of thalassemia in Southeast Asia. [Article]
Role of althernatively spliced bE-globin mRNA on clinical severity of beta-thalassemia/hemoglobin E disease. [Article]
Alterations and pathology of thalassemic red cells : comparison between alpha- and beta-thalassemia. [Article]
Prenatal diagnosis for beta-thalassemia syndromes using HRP-labeled oligonucleotide probes at Siriraj Hospital. [Article]
The instability of the membrane skeleton in thalassemic red blood cells. [Article]
Globin chain turvocer in reticulocytes from patients with beta^o-thalassemia/Hb E disease. [Article]
Hydroxyurea increases hemoglobin F levels and improves the effectiveness of erythropoiesis in beta-thalassemia/hemoglobin E disease.[Article]
Hematological problems in Asian traditional medicine. In “Microcirculatory Approach to Asian Traditional Medicine : Strategy for the Scientific Evaluation”.[Article]
Lymphocytes in beta-thalassemia/Hb E: subpopulations and mitogen responses. [Article]
Presence of immunoglobulins, C3 and cytolytic C5b-9 complement components on the surface of erythrocytes from patients with beta-thalassaemia/Hb E disease. [Article]
The effect of histological processing on the form of iron in iron-loaded human tissues.[Article]
The unusual pathobiology of hemoglobin Constant Spring red blood cells. [Article]
Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine. [Article]
An in vitro study on thalassemic erythroid precursors in liquid culture.
[Article]
alpha-Thalassemia incidence in Southern Thailand by restriction endonuclease analysis of globin DNA from placental blood at Songklanagarind hospital. .[Article]
Detection of thalassemia genes using smeared blood film or leukocytes adhering to polysthylene fibers.[Article]
Difference in pattern of erythropoietin response between beta-thalassemia/hemoglobin E children and adults. [Article]
The possible evidence of endothelial cell activation and disturbance in thalassemia : an in vitro study. [Article]
Morphological alterations and apoptosis of endothelial cells induced by thalassemic serum in vitro. [Article]
Surface and total tissue factor activity of endothelial cells. [Article]
A double-blind placebo control trial of Dilazep in beta-thalassemia/hemoglobin E patients. [Article]
The effect of Dilazep in beta-thalassemia/hemoglobin E patients. [Article]
Whole blood viscosity in thalassemia. Proceedings: The Third Asian Congress for Microcirculation. [Article]
Renal function in adult beta-thalassemia/Hb E disease. [Article]
Prenatal and postnatal diagnoses of thalassemias and hemoglobinopathies by HPLC. [Article]
Detection of z-globin chains in the cord blood by ELISA (enzyme-linked immunosorbent assay): rapid screening for alpha-thalassemia 1 (Southeast Asian type). [Article]
Molecular basis of beta-thalassemia in the Maldives. [Article]
Alpha and beta-thalassemia in Thailand. [Article]
Membrane phospholipid asymmetry in human thalassemia.[Article]
The form iron oxide deposits in thalassemia tissues varies between different groups of patients: a comparison between Thai ?-thalassemia/hemoglobin E patients and Australian ?-thalassemia [Article]
The course of anaemia after the treatment of acute, falciparum malaria.[Article]
Effects of alpha-thalassemia on pharmacokinetics of the antimalarial agent artesunate.[Article]
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