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
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145
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146
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147
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Thalassemic serum impairs endothelial cell growth in vitro.
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Prenatal diagnosis of the fetus at risk for beta-thalassemia/hemoglobin E disease: a report of the first case in Thailand.
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J Med Assoc Thai
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149
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Nondeletional type of hereditary persistence of fetal haemoglobin: molecular characterization of three unrelated Thai HPFH.
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150
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Plasma renin activity in patients with beta-thalassemia hemoglobin E.
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Hb Q-Thailand [alpha 74(EF3)Asp-->His]: gene organization, molecular structure, and DNA diagnosis.
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153
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Morphological assessment of platelet activation in thalassemia.
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Southeast Asian J Trop Med Public Health
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154
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Association of Hb Hope [beta136(H14)Gly-->Asp] and Hb H disease.
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Interaction of the alpha2 polyadenylation signal mutation (AATAAA-->AATA--) and alpha0-thalassemia (--SEA), resulting in Hb H disease in a Thai patient.
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157
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Studies of hemoglobin Bart and deletion of alpha-globin genes from cord blood in Thailand.
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Expression of hemoglobin E in newborn.
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161
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Analysis of hematological data of thalassemia cases in Thailand.
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Decreased heat stability found in purified hemoglobin Queens [alpha 34(B15)Leu----Arg].
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Erythrocyte volume and haemoglobin concentration in haemoglobin H disease: discrimination between the two genotypes.
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Acta Haematol
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169
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Lung function tests in splenectomized beta-thalassemia/Hb E patients.
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170
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Bioequivalence study of a film-coated tablet of deferiprone in healthy Thai volunteers.
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Int J Clin Pharmacol Ther
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171
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Inhibitory effect of beta zero-thalassaemia/haemoglobin E erythrocytes on Plasmodium falciparum growth in vitro.
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Trans R Soc Trop Med Hyg
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0.75
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172
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Molecular basis of beta-thalassemia in Japan: heterogeneity and origins of mutations.
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Acta Haematol
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Bam HI polymorphism of the beta A-, beta E-, and beta (0) -thalassemia genes in the Thai population.
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Birth Defects Orig Artic Ser
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0.75
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174
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Double heterozygosity for hemoglobin E and a Lepore-type hemoglobin found in a Thai woman.
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1987
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0.75
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175
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Antibody response in beta-thalassemia/Hb E disease, hemoglobin H patients, and nonthalassemics with enteric fever.
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1987
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176
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Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous fistula.
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J Med Assoc Thai
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177
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Glomerulonephritis in beta-thalassemia Hb-E disease: clinical manifestations, histopathologic studies and outcome.
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J Med Assoc Thai
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178
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Determination for different severity of anemia in thalassemia: concordance and discordance among sib pairs.
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Am J Med Genet
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179
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Biophysical changes of red cells with thalassemia-like abnormal hemoglobin.
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180
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Viral infections in beta-thalassemia/hemoglobin E patients.
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Birth Defects Orig Artic Ser
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181
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Molecular analysis of the human fetal-to-adult globin switching.
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Southeast Asian J Trop Med Public Health
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182
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Liver tissue injury secondary to iron overload in beta-thalassemia/hemoglobin E disease.
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Southeast Asian J Trop Med Public Health
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0.75
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183
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Red cell and plasma calcium, copper and zinc in beta-thalassemia/hemoglobin E.
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Southeast Asian J Trop Med Public Health
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184
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Detection of thalassemia genes using smeared blood film or leukocytes adhering to polysthylene fibers.
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Lymphocyte-bearing ferritin in beta-thalassemia/Hb E.
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J Med Assoc Thai
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Modified technique for detecting red cells containing inclusion bodies in alpha-thalassemia trait.
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0.75
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187
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Cord blood study on beta-thalassemia and hemoglobin E.
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Am J Med Genet
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1988
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Automatic measurement of hemoglobin F in blood obtained from patients with hemoglobin E/E and beta-thalassemia/hemoglobin/E.
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Southeast Asian J Trop Med Public Health
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1992
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0.75
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189
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Altered structure of spectrin in the two types of hemoglobin H disease.
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0.75
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190
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Erythrocyte glucose-6-phosphate dehydrogenase and pyruvate kinase activities in hemoglobin H disease.
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Southeast Asian J Trop Med Public Health
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0.75
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191
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Alpha-mRNA level in the two types of Hb H disease.
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192
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Brain pathology in 6 fatal cases of post-transfusion hypertension, convulsion and cerebral hemorrhage syndrome.
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Identification of Hb Anantharaj [alpha 11(A9)Lys->Glu] as Hb J-Wenchang-Wuming [alpha 11(A9)Lys->Gln].
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Beta 0-thalassemia due to a cytosine deletion in codon 41 associated with hemoglobin E.
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Cytochemical evaluation of neutrophil components in beta thalassemia hemoglobin E.
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Hb Siam [alpha15(A13)Gly-->Arg] is a GGT-->CGT mutation in the alpha1-globin gene.
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Morphology and kinetics of erythropoiesis in haemoglobin H disease.
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Improved technic for detecting intraerythrocytic inclusion bodies in alpha thalassemia trait.
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Heterogeneity of beta thalassaemia in Thailand.
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0.75
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The morphology of redox-dye-treated HbH-containing red cells: differences between cells treated with brilliant cresyl blue, methylene blue and new methylene blue.
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Clin Lab Haematol
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0.75
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202
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High-dose intravenous immunoglobulin in the management of immune hemolysis in patients with thalassemic disease: factors which determine refractoriness.
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0.75
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204
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Red blood cell microparticles in hemoglobin E disorders.
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0.75
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206
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The molecular basis of thalassemias.
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A double-blind placebo control trial of dilazep in beta-thalassemia/hemoglobin E patients.
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Intracranial extramedullary hematopoiesis in beta-thalassemia/hemoglobin E disease.
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Rapid differentiation of five common alpha-thalassemia genotypes by polymerase chain reaction.
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An in vitro study on thalassemic erythroid precursors in liquid culture.
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