S Fucharoen

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Top papers

Rank Title Journal Year PubWeight™‹?›
1 ICSH recommendations for the measurement of haemoglobin A2. Int J Lab Hematol 2011 2.23
2 Membrane phospholipid asymmetry in human thalassemia. Blood 1998 1.36
3 Mitochondrial DNA polymorphisms in Thailand. J Hum Genet 2001 1.26
4 Restoration of hemoglobin A synthesis in erythroid cells from peripheral blood of thalassemic patients. Proc Natl Acad Sci U S A 2000 1.22
5 Asymmetrically primed selective amplification/temperature shift fluorescence polymerase chain reaction to detect the hemoglobin Constant Spring mutation. Blood 1991 1.20
6 Hemoglobinopathies in Southeast Asia. Hemoglobin 1987 1.16
7 Fatal arteritis due to Pythium insidiosum infection in patients with thalassaemia. Trans R Soc Trop Med Hyg 1993 1.12
8 The effect of erythroid hyperplasia on iron balance. Blood 1988 1.06
9 Genetic factors affecting clinical severity in beta-thalassemia syndromes. J Pediatr Hematol Oncol 2000 1.05
10 Molecular and hematologic features of hemoglobin E heterozygotes with different forms of alpha-thalassemia in Thailand. Ann Hematol 2003 1.04
11 A multi-center study in order to further define the molecular basis of beta-thalassemia in Thailand, Pakistan, Sri Lanka, Mauritius, Syria, and India, and to develop a simple molecular diagnostic strategy by amplification refractory mutation system-polymerase chain reaction. Hemoglobin 2001 1.02
12 Molecular basis of beta-thalassemia in the Maldives. Hemoglobin 1998 1.01
13 The unusual pathobiology of hemoglobin constant spring red blood cells. Blood 1997 0.99
14 Impaired parasite growth and increased susceptibility to phagocytosis of Plasmodium falciparum infected alpha-thalassemia or hemoglobin Constant Spring red blood cells. Am J Clin Pathol 1988 0.99
15 Hematologic and biosynthetic studies in homozygous hemoglobin Constant Spring. J Clin Invest 1984 0.98
16 Pulmonary artery obstruction in thalassaemia. Southeast Asian J Trop Med Public Health 1980 0.98
17 Beta-globin gene cluster polymorphisms are strongly associated with severity of HbE/beta(0)-thalassemia. Clin Genet 2007 0.96
18 Pulmonary thromboembolism in thalassemic patients. Southeast Asian J Trop Med Public Health 1992 0.95
19 Red cell deformability, splenic function and anaemia in thalassaemia. Br J Haematol 1999 0.95
20 Beta-thalassemia in Thailand. Ann N Y Acad Sci 1990 0.93
21 Thalassemia in Thailand. Ann N Y Acad Sci 1980 0.93
22 Prevalence of HTLV-III/LAV antibody in selected populations in Thailand. Southeast Asian J Trop Med Public Health 1985 0.91
23 Serum levels of tumor necrosis factor-alpha, interleukin-1, and interferon-gamma in beta(o)-thalassemia/HbE and their clinical significance. J Interferon Cytokine Res 1999 0.91
24 Molecular characterization of hemoglobin C in Thailand. Am J Hematol 2001 0.91
25 The instability of the membrane skeleton in thalassemic red blood cells. Blood 1995 0.91
26 The fate of excess beta-globin chains within erythropoietic cells in alpha-thalassaemia 2 trait, alpha-thalassaemia 1 trait, haemoglobin H disease and haemoglobin Q-H disease: an electron microscope study. Br J Haematol 1984 0.91
27 Liver injury due to iron overload in thalassemia: histopathologic and ultrastructural studies. Biometals 1996 0.90
28 Severity differences in beta-thalassaemia/haemoglobin E syndromes: implication of genetic factors. Br J Haematol 1993 0.90
29 Decreased sensitivity of artesunate and chloroquine of Plasmodium falciparum infecting hemoglobin H and/or hemoglobin constant spring erythrocytes. J Clin Invest 1989 0.90
30 Possible evidence of endothelial cell activation and disturbance in thalassemia: an in vitro study. Southeast Asian J Trop Med Public Health 1997 0.89
31 Major hematologic diseases in the developing world- new aspects of diagnosis and management of thalassemia, malarial anemia, and acute leukemia. Hematology Am Soc Hematol Educ Program 2001 0.89
32 Screening for the carriers of thalassemias and abnormal hemoglobins at the community level. Southeast Asian J Trop Med Public Health 2002 0.89
33 Impairment of Plasmodium falciparum growth in thalassemic red blood cells: further evidence by using biotin labeling and flow cytometry. Blood 1999 0.89
34 Increased circulating platelet aggregates in thalassaemia. Southeast Asian J Trop Med Public Health 1981 0.88
35 Prenatal diagnosis of beta-thalassaemia by reverse dot-blot hybridization. Prenat Diagn 1999 0.88
36 Lymphocyte subsets and specific T-cell immune response in thalassemia. Cytometry 2000 0.88
37 Renal function in adult beta-thalassemia/Hb E disease. Nephron 1998 0.87
38 Ultrastructure and cell cycle distribution of erythropoietic cells in heterozygotes and homozygotes for haemoglobin E. Br J Haematol 1984 0.87
39 Concomitant inheritance of alpha-thalassemia in beta 0- thalassemia/Hb E disease. Am J Hematol 1985 0.86
40 Epigallocatechin-3-gallate and epicatechin-3-gallate from green tea decrease plasma non-transferrin bound iron and erythrocyte oxidative stress. Med Chem 2007 0.85
41 Alterations in vascular endothelial cell-related plasma proteins in thalassaemic patients and their correlation with clinical symptoms. Thromb Haemost 1995 0.85
42 Increase in spontaneous platelet aggregation in beta-thalassemia/hemoglobin E disease: a consequence of splenectomy. Southeast Asian J Trop Med Public Health 1992 0.85
43 Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system. Int J Lab Hematol 2011 0.84
44 Identification of five rare mutations including a novel frameshift mutation causing beta zero-thalassemia in Thai patients with beta zero-thalassemia/hemoglobin E disease. Biochim Biophys Acta 1992 0.84
45 Hypoxemia in thalassemia. Birth Defects Orig Artic Ser 1982 0.84
46 Simple non-radioactive method for detecting haemoglobin Constant Spring gene. Lancet 1990 0.84
47 Thalassemia in southeast Asia: determination of different degrees of severity of anemia in thalassemia. Ann N Y Acad Sci 1985 0.84
48 Thai G gamma (A gamma delta beta)zero-thalassemia and its interaction with a single gamma-globin gene on a chromosome carrying beta zero-thalassemia. Hemoglobin 1990 0.84
49 Identification of Hb J-Buda [alpha61(E10)Lys-->Asn] in a Thai female. Hemoglobin 1999 0.83
50 Oxidative stress and antioxidants in beta-thalassaemia/haemoglobin E. J Med Assoc Thai 1987 0.83
51 Effect of green tea on iron status and oxidative stress in iron-loaded rats. Med Chem 2008 0.83
52 Hypoxaemia and the effect of aspirin in thalassaemia. Southeast Asian J Trop Med Public Health 1981 0.83
53 Intracranial extramedullary hematopoiesis inducing epilepsy in a patient with beta-thalassemia--hemoglobin E. Arch Intern Med 1985 0.82
54 Reverse dot-blot detection of Thai beta-thalassaemia mutations. Br J Haematol 1995 0.82
55 Molecular mechanisms of thalassemia in southeast Asia. Southeast Asian J Trop Med Public Health 1995 0.82
56 Molecular analysis of alpha-thalassemia in Nepal: correlation with malaria endemicity. J Hum Genet 2000 0.82
57 Haemoglobin-E trait and the clinical course of malaria in Thai soldiers. Eur J Haematol 1990 0.82
58 Alpha-thalassemia incidence in southern Thailand by restriction endonuclease analysis of globin DNA from placental blood at Songklanagarind Hospital. Southeast Asian J Trop Med Public Health 1997 0.81
59 Effects of green tea on iron accumulation and oxidative stress in livers of iron-challenged thalassemic mice. Med Chem 2010 0.81
60 Maternal uniparental disomy of chromosome 16 resulting in hemoglobin Bart's hydrops fetalis. Clin Genet 2008 0.81
61 Role of NF-kappa B in regulation of apoptosis of erythroid progenitor cells. Eur J Haematol 2005 0.80
62 Cytoadherence between endothelial cells and P. falciparum infected and noninfected normal and thalassemic red blood cells. Cytometry B Clin Cytom 2006 0.80
63 Erythroblast- and erythrocyte-bound antibodies in alpha and beta thalassaemia syndromes. Transfus Med 1991 0.80
64 Reversal of cardiac iron loading and dysfunction in thalassemic mice by curcuminoids. Med Chem 2011 0.80
65 Curcumin contributes to in vitro removal of non-transferrin bound iron by deferiprone and desferrioxamine in thalassemic plasma. Med Chem 2007 0.80
66 Ultrasonographic method for detection of haemoglobin Bart's hydrops fetalis in the second trimester of pregnancy. Prenat Diagn 1990 0.80
67 Rapid and simultaneous non-radioactive method for detecting alpha-thalassemia 1 (SEA type) and Hb Constant Spring genes. Eur J Haematol 1994 0.80
68 A study of thalassemia associated with pregnancy. Birth Defects Orig Artic Ser 1988 0.80
69 Cardiac involvement in beta-thalassemia/hemoglobin E disease: clinical and hemodynamic findings. Southeast Asian J Trop Med Public Health 1990 0.80
70 Molecular basis of HbE-beta-thalassemia and the origin of HbE in northeast Thailand: identification of one novel mutation using amplified DNA from buffy coat specimens. Biochem Biophys Res Commun 1990 0.80
71 Study of mechanisms of post-transfusion hypertension in thalassaemic patients. Southeast Asian J Trop Med Public Health 1989 0.80
72 Homozygous haemoglobin Constant Spring: a need for revision of concept. Hum Genet 1981 0.79
73 Difference in pattern of erythropoietin response between beta-thalassemia/hemoglobin E children and adults. Southeast Asian J Trop Med Public Health 1997 0.79
74 The molecular basis of beta-thalassemia in Thailand: application to prenatal diagnosis. Am J Hum Genet 1990 0.79
75 Different severity of homozygous beta-thalassemia among siblings. Hum Genet 1987 0.79
76 Distribution of pulmonary thromboembolic lesions in thalassemic patients. Birth Defects Orig Artic Ser 1987 0.79
77 Detection of beta-thalassemia and hemoglobin E genes in Thai by a DNA amplification technique. Hum Genet 1989 0.79
78 Simultaneous PCR detection of beta - thalassemia and alpha - thalassemia 1 (SEA type) in prenatal diagnosis of complex thalassemia syndrome. Clin Biochem 2001 0.79
79 Molecular basis of alpha (0)-thalassemia in northeast of Thailand. Southeast Asian J Trop Med Public Health 1995 0.79
80 Thalassemic erythrocytes inhibit in vitro growth of Plasmodium falciparum. J Clin Microbiol 1987 0.79
81 Increased phagocytosis of Plasmodium falciparum-infected erythrocytes with haemoglobin E by peripheral blood monocytes. Acta Haematol 1986 0.79
82 Molecular and hematological characterization of HbE heterozygote with alpha-thalassemia determinant. Southeast Asian J Trop Med Public Health 1997 0.78
83 Increased serum levels of macrophage colony-stimulating factor (M-CSF) in alpha- and beta-thalassaemia syndromes: correlation with anaemia and monocyte activation. Eur J Haematol 1996 0.78
84 Reduced deformability of thalassemic erythrocytes and erythrocytes with abnormal hemoglobins and relation with susceptibility to Plasmodium falciparum invasion. Blood 1992 0.78
85 Role of FcgammaRI (CD64) in erythrocyte elimination and its up-regulation in thalassaemia. Br J Haematol 1999 0.78
86 Comparison of erythrocyte antioxidative enzyme activities between two types of haemoglobin H disease. J Clin Pathol 1986 0.78
87 Oxidative stress and antioxidative enzymes in hemoglobin H disease. Birth Defects Orig Artic Ser 1987 0.78
88 Molecular basis of beta-thalassemia in Thailand. Birth Defects Orig Artic Ser 1987 0.77
89 Alterations and pathology of thalassemic red cells: comparison between alpha- and beta-thalassemia. Southeast Asian J Trop Med Public Health 1995 0.77
90 Hemoglobin constant spring in Bangkok: molecular screening by selective enzymatic amplification of the alpha 2-globin gene. Am J Hematol 1991 0.77
91 Study of hematopoietic progenitors in patients with thalassemia: the effect of splenectomy. Birth Defects Orig Artic Ser 1988 0.77
92 Hydration of red cells in alpha and beta thalassemias differs. A useful approach to distinguish between these red cell phenotypes. Am J Clin Pathol 1994 0.77
93 Role of alternatively spliced beta E-globin mRNA on clinical severity of beta-thalassemia/hemoglobin E disease. Southeast Asian J Trop Med Public Health 1995 0.77
94 Number and maturation of reticulocytes in various genotypes of thalassaemia as assessed by flow cytometry. Acta Haematol 1994 0.77
95 Morphological alterations and apoptosis of endothelial cells induced by thalassemic serum in vitro. Southeast Asian J Trop Med Public Health 1997 0.77
96 Identification of Hb C [beta 6(A3)Glu-->Lys] in a Thai male. Hemoglobin 1993 0.77
97 Increase in non-transferrin bound iron and the oxidative stress status in epilepsy patients treated using valproic acid monotherapy. Int J Clin Pharmacol Ther 2011 0.77
98 Identification of Hb Lepore-Washington-Boston in association with Hb E [beta 26(B8)Glu----Lys] in a Thai female. Hemoglobin 1987 0.77
99 Determination of variable severity of anemia in thalassemia: erythrocyte proteolytic activity. Birth Defects Orig Artic Ser 1987 0.77
100 Pituitary function in thalassemic patients and the effect of chelation therapy. Acta Endocrinol (Copenh) 1991 0.77
101 Cardiac pathology in 47 patients with beta thalassaemia/haemoglobin E. Southeast Asian J Trop Med Public Health 1984 0.77
102 Detection of haemoglobin variants and inference of their functional properties using complete oxygen dissociation curve measurements. Br J Haematol 2001 0.77
103 Selective enzymatic amplification of alpha 2-globin DNA for detection of the hemoglobin Constant Spring mutation. Blood 1989 0.77
104 Molecular characterization of thalassemia intermedia with homozygous Hb Malay and Hb Malay/HbE in Thai patients. Haematologica 2001 0.77
105 Histochemical study of liver tissue from thalassemic patients. Birth Defects Orig Artic Ser 1988 0.77
106 Severe infection in thalassemia: a prospective study. Birth Defects Orig Artic Ser 1987 0.77
107 Compound heterozygosity for Hb Korle-Bu (beta(73); Asp-Asn) and Hb E (beta(26); Glu-Lys) with a 3.7-kb deletional alpha-thalassemia in Thai patients. Ann Hematol 2002 0.76
108 Differential expression of erythrocyte calpain and calpastatin activities in beta 0-thalassemia/Hb E disease. Birth Defects Orig Artic Ser 1987 0.76
109 Lymphocytes in beta-thalassemia/HbE: subpopulations and mitogen responses. Eur J Haematol 1996 0.76
110 The molecular basis of alpha-thalassemia in Thailand. Southeast Asian J Trop Med Public Health 1992 0.76
111 Molecular heterogeneity of beta-thalassemia in Thailand. Southeast Asian J Trop Med Public Health 1992 0.76
112 Cholecystectomy in thalassemia. Birth Defects Orig Artic Ser 1988 0.76
113 Detection of PF3 availability in whole blood from volunteers and beta-thalassemia/HbE patients: a promising method for prediction of thrombotic tendency. Southeast Asian J Trop Med Public Health 1992 0.76
114 Activation of monocytes for the immune clearance of red cells in beta zero-thalassaemia/HbE. Br J Haematol 1993 0.76
115 Efficacy of curcuminoids in alleviation of iron overload and lipid peroxidation in thalassemic mice. Med Chem 2009 0.76
116 Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand. Clin Lab Haematol 2004 0.76
117 Heterogeneity of the gamma-globin gene sequences in Japanese individuals: implication of gene conversion in generation of polymorphisms. J Biochem 1989 0.76
118 Thalassemic serum inhibits endothelial cell mitosis in vitro. Southeast Asian J Trop Med Public Health 1997 0.76
119 Flow cytometric immunophenotyping of lymphocyte subsets in samples that contain a high proportion of non-lymphoid cells. Cytometry 1994 0.76
120 Detection of alpha-thalassemia-1 (Southeast Asian type) and its application for prenatal diagnosis. Clin Genet 1995 0.76
121 Three-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta gunma) with a thalassemia-like phenotype. Blood 1990 0.76
122 ICSH recommendations for the measurement of haemoglobin F. Int J Lab Hematol 2011 0.76
123 A study of infective episodes in patients with beta-thalassemia/Hb E disease in Thailand. Birth Defects Orig Artic Ser 1987 0.76
124 Gallstones in thalassemia. Birth Defects Orig Artic Ser 1988 0.76
125 The molecular basis of AE-Bart's disease. Hemoglobin 1989 0.76
126 Protein C and protein S deficiency in thalassemic patients. Southeast Asian J Trop Med Public Health 1992 0.75
127 Human genetic disease in Asia. Southeast Asian J Trop Med Public Health 1994 0.75
128 Clinical and hematological features of beta(+)-thalassemia (IVS-1 nt 5, G-C mutation) in Thai patients. Eur J Haematol 2001 0.75
129 Icsh activities and Asia. Southeast Asian J Trop Med Public Health 1999 0.75
130 Presence of immunoglobulins, C3 and cytolytic C5b-9 complement components on the surface of erythrocytes from patients with beta-thalassaemia/HbE disease. Br J Haematol 1997 0.75
131 Hemoglobin Dhonburi alpha 2 beta 2 126 (H4) Val----Gly: a new unstable beta variant producing a beta-thalassemia intermedia phenotype in association with beta zero-thalassemia. Am J Hematol 1990 0.75
132 Cross over placebo control trial of dilazep in beta-thalassemia/hemoglobin E patients. Southeast Asian J Trop Med Public Health 1999 0.75
133 No evidence for a role of disulfide bonds in the attachment of inclusion bodies to the red cell membrane. Birth Defects Orig Artic Ser 1987 0.75
134 Genetic compound heterozygosity for Southeast Asian ovalocytosis and thalassemia in Thailand: prevalence and phenotypic analysis. Clin Genet 2013 0.75
135 DNA polymorphisms of beta N- and beta E-globin genes in Thais. Birth Defects Orig Artic Ser 1987 0.75
136 Clinical and hematological features of codon 17, A-T mutation of beta-thalassemia in Thai patients. Eur J Haematol 2001 0.75
137 Studies of erythropoietic cells in heterozygotes and homozygotes for haemoglobin Constant Spring and in heterozygotes for both haemoglobin Constant Spring and alpha-thalassaemia 1 trait: extent of globin chain precipitation and cell cycle distribution. Clin Lab Haematol 1986 0.75
138 Relation between erythropoiesis and bone metabolism in thalassemia. N Engl J Med 1981 0.75
139 Pathogenesis of hypoxemia. Southeast Asian J Trop Med Public Health 1992 0.75
140 Impaired glucose counterregulation after insulin-induced hypoglycemia in thalassemic patients. J Med Assoc Thai 1987 0.75
141 Hb G-Coushatta [beta22(B4)Glu-->Ala] in Thailand. Hemoglobin 1999 0.75
142 Electron microscopic study of liver tissue from 30 thalassemic patients. Birth Defects Orig Artic Ser 1988 0.75
143 Hemoglobin Bart disease without hydrops manifestation. Birth Defects Orig Artic Ser 1987 0.75
144 Detection and structural analysis of abnormal hemoglobins found in Thailand. Southeast Asian J Trop Med Public Health 1999 0.75
145 Globin chain turnover in reticulocytes from patients with beta (0) -thalassaemia/Hb E disease. Eur J Haematol 1995 0.75
146 Fetal red cell staining: method evaluation. J Med Assoc Thai 1992 0.75
147 Thalassemic serum impairs endothelial cell growth in vitro. Southeast Asian J Trop Med Public Health 1992 0.75
148 Prenatal diagnosis of the fetus at risk for beta-thalassemia/hemoglobin E disease: a report of the first case in Thailand. J Med Assoc Thai 1987 0.75
149 Nondeletional type of hereditary persistence of fetal haemoglobin: molecular characterization of three unrelated Thai HPFH. Br J Haematol 1994 0.75
150 Plasma renin activity in patients with beta-thalassemia hemoglobin E. Birth Defects Orig Artic Ser 1988 0.75
151 Beta-globin gene haplotypes in some minor ethnic groups in Thailand. Southeast Asian J Trop Med Public Health 1997 0.75
152 Hb Q-Thailand [alpha 74(EF3)Asp-->His]: gene organization, molecular structure, and DNA diagnosis. Hemoglobin 1992 0.75
153 Morphological assessment of platelet activation in thalassemia. Southeast Asian J Trop Med Public Health 1992 0.75
154 Association of Hb Hope [beta136(H14)Gly-->Asp] and Hb H disease. Hemoglobin 2001 0.75
155 Effects of thalassaemic serum on the in vitro development of the malarial parasite Plasmodium falciparum. Parasitol Res 1989 0.75
156 Interaction of the alpha2 polyadenylation signal mutation (AATAAA-->AATA--) and alpha0-thalassemia (--SEA), resulting in Hb H disease in a Thai patient. Hemoglobin 2001 0.75
157 Studies of hemoglobin Bart and deletion of alpha-globin genes from cord blood in Thailand. Birth Defects Orig Artic Ser 1987 0.75
158 Expression of hemoglobin E in newborn. Southeast Asian J Trop Med Public Health 1995 0.75
159 Oropharyngeal colonization with aerobic bacteria in beta-thalassemia/hemoglobin E disease. Birth Defects Orig Artic Ser 1987 0.75
160 Size distribution curves of blood cells in thalassemias and hemoglobin H diseases. Southeast Asian J Trop Med Public Health 1992 0.75
161 Analysis of hematological data of thalassemia cases in Thailand. Nihon Ketsueki Gakkai Zasshi 1989 0.75
162 Ineffective erythropoiesis in haemoglobin E beta -thalassaemia: an electron microscope study. Br J Haematol 1981 0.75
163 Lung perfusion in thalassemia. Birth Defects Orig Artic Ser 1987 0.75
164 Surface and total tissue factor activity of endothelial cells. Southeast Asian J Trop Med Public Health 1997 0.75
165 Decreased heat stability found in purified hemoglobin Queens [alpha 34(B15)Leu----Arg]. Hemoglobin 1987 0.75
166 Alpha-thalassemia in Thailand. Hemoglobin 1988 0.75
167 Hemostatic alterations in beta-thalassemia/hemoglobin E patients. Southeast Asian J Trop Med Public Health 1999 0.75
168 Erythrocyte volume and haemoglobin concentration in haemoglobin H disease: discrimination between the two genotypes. Acta Haematol 1992 0.75
169 Lung function tests in splenectomized beta-thalassemia/Hb E patients. Birth Defects Orig Artic Ser 1987 0.75
170 Bioequivalence study of a film-coated tablet of deferiprone in healthy Thai volunteers. Int J Clin Pharmacol Ther 2009 0.75
171 Inhibitory effect of beta zero-thalassaemia/haemoglobin E erythrocytes on Plasmodium falciparum growth in vitro. Trans R Soc Trop Med Hyg 1987 0.75
172 Molecular basis of beta-thalassemia in Japan: heterogeneity and origins of mutations. Acta Haematol 1994 0.75
173 Bam HI polymorphism of the beta A-, beta E-, and beta (0) -thalassemia genes in the Thai population. Birth Defects Orig Artic Ser 1987 0.75
174 Double heterozygosity for hemoglobin E and a Lepore-type hemoglobin found in a Thai woman. Birth Defects Orig Artic Ser 1987 0.75
175 Antibody response in beta-thalassemia/Hb E disease, hemoglobin H patients, and nonthalassemics with enteric fever. Birth Defects Orig Artic Ser 1987 0.75
176 Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous fistula. J Med Assoc Thai 1982 0.75
177 Glomerulonephritis in beta-thalassemia Hb-E disease: clinical manifestations, histopathologic studies and outcome. J Med Assoc Thai 1995 0.75
178 Determination for different severity of anemia in thalassemia: concordance and discordance among sib pairs. Am J Med Genet 1984 0.75
179 Biophysical changes of red cells with thalassemia-like abnormal hemoglobin. Southeast Asian J Trop Med Public Health 1992 0.75
180 Viral infections in beta-thalassemia/hemoglobin E patients. Birth Defects Orig Artic Ser 1987 0.75
181 Molecular analysis of the human fetal-to-adult globin switching. Southeast Asian J Trop Med Public Health 1995 0.75
182 Liver tissue injury secondary to iron overload in beta-thalassemia/hemoglobin E disease. Southeast Asian J Trop Med Public Health 1992 0.75
183 Red cell and plasma calcium, copper and zinc in beta-thalassemia/hemoglobin E. Southeast Asian J Trop Med Public Health 1991 0.75
184 Detection of thalassemia genes using smeared blood film or leukocytes adhering to polysthylene fibers. Southeast Asian J Trop Med Public Health 1997 0.75
185 Lymphocyte-bearing ferritin in beta-thalassemia/Hb E. J Med Assoc Thai 1992 0.75
186 Modified technique for detecting red cells containing inclusion bodies in alpha-thalassemia trait. Birth Defects Orig Artic Ser 1987 0.75
187 Cord blood study on beta-thalassemia and hemoglobin E. Am J Med Genet 1988 0.75
188 Automatic measurement of hemoglobin F in blood obtained from patients with hemoglobin E/E and beta-thalassemia/hemoglobin/E. Southeast Asian J Trop Med Public Health 1992 0.75
189 Altered structure of spectrin in the two types of hemoglobin H disease. Birth Defects Orig Artic Ser 1987 0.75
190 Erythrocyte glucose-6-phosphate dehydrogenase and pyruvate kinase activities in hemoglobin H disease. Southeast Asian J Trop Med Public Health 1992 0.75
191 Alpha-mRNA level in the two types of Hb H disease. Birth Defects Orig Artic Ser 1987 0.75
192 Brain pathology in 6 fatal cases of post-transfusion hypertension, convulsion and cerebral hemorrhage syndrome. Southeast Asian J Trop Med Public Health 1992 0.75
193 Identification of Hb Anantharaj [alpha 11(A9)Lys->Glu] as Hb J-Wenchang-Wuming [alpha 11(A9)Lys->Gln]. Hemoglobin 1993 0.75
194 Beta 0-thalassemia due to a cytosine deletion in codon 41 associated with hemoglobin E. Southeast Asian J Trop Med Public Health 1993 0.75
195 Cytochemical evaluation of neutrophil components in beta thalassemia hemoglobin E. J Med Assoc Thai 1989 0.75
196 Hb Siam [alpha15(A13)Gly-->Arg] is a GGT-->CGT mutation in the alpha1-globin gene. Hemoglobin 2000 0.75
197 Morphology and kinetics of erythropoiesis in haemoglobin H disease. Br J Haematol 1981 0.75
198 Fetal red cell in Thai thalassemia trait patients. Acta Haematol 1991 0.75
199 Improved technic for detecting intraerythrocytic inclusion bodies in alpha thalassemia trait. J Med Assoc Thai 1985 0.75
200 Heterogeneity of beta thalassaemia in Thailand. Southeast Asian J Trop Med Public Health 1982 0.75
201 The morphology of redox-dye-treated HbH-containing red cells: differences between cells treated with brilliant cresyl blue, methylene blue and new methylene blue. Clin Lab Haematol 1985 0.75
202 Interaction between endothelial cells and thalassemic red cells in vitro. Southeast Asian J Trop Med Public Health 1992 0.75
203 High-dose intravenous immunoglobulin in the management of immune hemolysis in patients with thalassemic disease: factors which determine refractoriness. Southeast Asian J Trop Med Public Health 1991 0.75
204 Red blood cell microparticles in hemoglobin E disorders. Int J Lab Hematol 2014 0.75
205 Defective spectrin dimer self-association in thalassemic red cells. Eur J Haematol 1987 0.75
206 The molecular basis of thalassemias. Indian J Pediatr 1990 0.75
207 Oxidative stress and antioxidants in beta-thalassemia/hemoglobin E. Birth Defects Orig Artic Ser 1987 0.75
208 Cholecystitis associated with Enterobacter agglomerans. Southeast Asian J Trop Med Public Health 1984 0.75
209 Detection of zeta-globin chains in the cord blood by ELISA (enzyme-linked immunosorbent assay): rapid screening for alpha-thalassemia 1 (Southeast Asian type). Am J Hematol 1998 0.75
210 A double-blind placebo control trial of dilazep in beta-thalassemia/hemoglobin E patients. Southeast Asian J Trop Med Public Health 1997 0.75
211 Prenatal diagnosis for beta-thalassemia syndromes using HRP-labeled oligonucleotide probes at Siriraj Hospital. Southeast Asian J Trop Med Public Health 1995 0.75
212 Intracranial extramedullary hematopoiesis in beta-thalassemia/hemoglobin E disease. Am J Hematol 1981 0.75
213 Molecular basis of beta (0)-thalassemia/HbE disease in Thailand. Biochem Biophys Res Commun 1989 0.75
214 Rapid differentiation of five common alpha-thalassemia genotypes by polymerase chain reaction. J Lab Clin Med 2001 0.75
215 An in vitro study on thalassemic erythroid precursors in liquid culture. Southeast Asian J Trop Med Public Health 1997 0.75
216 Clinical and hematologic features of beta0-thalassemia (frameshift 41/42 mutation) in Thai patients. Haematologica 2001 0.75