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ผลงานวิชาการ
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His Majesty the King and the New Development Code
This article is the translation of a transcribed speech given by Dr.Pravet Wasii at the Plaza Athinee Hotel on July 24, 2006, to celebrate the 60th anniversary of HM King Bhumibol Adulyadej’s reign. The editorial board of MANUSYA is grateful for Dr. Pravet Wasii’s contribution. The translation printed here remains for the most part unedited. -
Genetic Factors Affecting Clinical Severity in β-Thalassemia Syndromes
This study was Supported by grants from the National Research Council of Thailand, International Atomic Energy Agency, and Prajadhipok-Rambhai Barni Foundation. -
Clinical Manifestation of β-Thalassemia/Hemoglobin E Disease
This article was supported by grants from Prajadhipok-Rambhai Barni Foundation and National Center for Genetic Engineering and Biotechnology. -
A correlation of erythrokinetics, ineffective erythropoiesis, and erythroid precursor apoptosis in Thai patients with thalassemia
This article was presented in part at the XXI Congress of the International Society of Hematology, Sydney, Australia, May 1985, and the Annual Meeting of the American Society of Hematology, San Diego, CA, December 1997. -
Presence of immunoglobulins, C3 and cytolytic C5b-9 complement components on the surface of erythrocytes from patients with β-thalassaemia/HbE disease
This study was supported by the USPHS Research Grant HL34408 from the Heart, Lung, and Blood Institute, U.S.A., the Deutsche Forschungsgemeinschaft (SFB 311, project D10) and the Verband der Chemischen Industrie. -
Severity differences in β-thalassaemia/haemoglobin E syndromes: implication of genetic factors
This study was partially supported by the U.S. Public Health research grant HL 34408 from the National Heart, Lung, and Blood Institute and the Commission of the European Communities, Science and Technology for the Development Program. contract No. TS2.013 1 .TH(H). Pranee (Winichagoon) Fucharoen was supported by JSPS Ph.D. dissertation (Ronpaku) program. -
Identification of five rare mutations including a novel frameshift mutation causing β0-thalassemia in Thai patients with β0-thalassemia/hemoglobin E disease
This research was supported in part by EEC grant TS 2. 0131. TH (H), U.S. Public Health Research Grant HL 34408 and by grants from the Ministry of Education, Science and Culture, Japan. -
β-Thalassemia in Thailand
This study was supported by U.S. Public Health Research Grant HL 34408 from the National Heart, Lung, and Blood Institute and CEC grant, Program Contract No. TS2.0131.TH(H). -
The effect of erythroid hyperplasia on iron balance
Supported by US Public Health Research Grant HL 34408 from the National Heart, Lung, and Blood Institute; National lnstitutes of Health Research Grant No. HL06242; a Travel Grant from Welcome Trust, London; and the International Atomic Energy Agency Fellowship Program of the National Research Council, National Academy of Sciences. -
Cord blood study on β-thalassemia and hemoglobin E
This work was supported by Thai National Research Council and in part by the US Public Health research grant HL 34408 from the National Heart, Lung and Blood Institute. -
Increased Phagocytosis of Plasmodium falciparum-Infected Erythrocytes with Haemoglobin E by Peripheral Blood Monocytes
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Bareheaded doctors
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Thalassemia in Southeast Asia: Determination of Different Degrees of Severity of Anemia in Thalassemia
This study was supported by US Public Health research grant AM 09805 from the National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases. -
Quantitative Changes of Red Blood Cell Shapes in Relation to Clinical Features in β-Thalassemia/HbE Disease
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Concomitant inheritance of α-thalassemia in β°-thalassemia/hb e disease
This study was supported by a US. Public Health Service research grant AM 09805 from the National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases. -
Increased Red Blood Cell Protoporphyrin in Thalassemia: A Result of Relative Iron Deficiency
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Determination for different severity of anemia in thalassemia: Concordance and discordance among sib pairs
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Different Patterns of Intraerythrocytic Inclusion Body Distribution in the Two Types of Haemoglobin H Disease: An Ultrastructural Study
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Spinal Cord Compression in Thalassemia: Report of 12 Cases and Recommendations for Treatment
The study was supported by Public Health Service research grant AM 09805 from the Institute of Arthritis, Metabolism, and Digestive Diseases -
Problems Of Haematology Training In Developing Countries
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Morphology and Kinetics of Erythropoiesis in Haemoglobin H Disease
This work was supported by a project grant (G979/92/S) from the Medical Research Council and a travel grant to S.N.W. from the British Council. The work done in Thailand was supported by a U.S. Public Health research grant (AM 09805) from the National Institute of Arthritis, Metabolism and Digestive Diseases. -
Intracranial extramedullary hematopoiesis in β°-thalassemia/hemoglobin E disease
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Ineffective Erythropoiesis in Haemoglobin Eβ -thalassaemia: an Electron Microscope Study
This work was supported by project grant no. G979/92/S from the Medical Research Council and a travel grant to S.N.W. from the British Council -
2 - Haemoglobinopathies Including Thalassaemia: Part 1: Tropical Asia
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Levels of haemoglobin H and proportions of red cells with inclusion bodies in the two types of haemoglobin H disease
This short communication was supported by a U.S. Public Health research grant AM 09805 from the Institute of Arthritis, Metabolism and Digestive Diseases.