Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine.
about
The inherited diseases of hemoglobin are an emerging global health burden.In silico analysis of single nucleotide polymorphism (SNPs) in human β-globin geneMitochondrial Changes in β0-Thalassemia/Hb E DiseaseA Novel -72 (T→A) β-Promoter Mutation Causing Slightly Elevated HbA2 in a Vietnamese HeterozygoteEvolution of haemoglobin function: molecular adaptations to environment.A mechanism of ineffective erythropoiesis in β-thalassemia/Hb E diseaseAge-related changes in adaptation to severe anemia in childhood in developing countriesThe thalassaemia syndromes.RNA repair restores hemoglobin expression in IVS2-654 thalassemic mice.Interaction of malaria with a common form of severe thalassemia in an Asian population.Sociodemographic profile and oral health status of thalassemic patients attending the National Thalassaemia Centre, Kurunegala, Sri Lanka.Molecular Characterization of β-Thalassemia Mutations in Central Vietnam.Fetal hemoglobin regulation in β-thalassemia: heterogeneity, modifiers and therapeutic approaches.Rapid diagnosis of alpha-thalassemia by melting curve analysis.Pattern of β-Thalassemia and Other Haemoglobinopathies: A Cross-Sectional Study in Bangladesh.Molecular analysis of beta-globin gene mutations among Thai beta-thalassemia children: results from a single center study.Fermented papaya preparation for β-thalassemia?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-Two cases of compound heterozygosity for Hb Hekinan [alpha27(B8)Glu-->Asp (alpha1)] and alpha-thalassemia in Thailand.Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Ggamma(Agammadeltabeta)0-thalassemia and Ggamma(Agammadeltabeta)0-thalassemia/HbE in Thai patients.A rare Hb H disease due to the - -(SEA) and 16.6 kb α-thalassemia-2 deletions.Identification of Hb Q-India (alpha64 Asp-->His) in Thailand.Development of hemoglobin typing control materials for laboratory investigation of thalassemia and hemoglobinopathies.Evolution of hematological parameters in HIV-1-infected patients with and without thalassemia carriages during highly active antiretroviral therapy.Acute haemolytic crisis in a Thai patient with homozygous haemoglobin Constant Spring (Hb CS/CS): a case report.Effect of health education on severe thalassemia prevention and control in communities in Cambodia.Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations.Prenatal diagnosis of beta-thalassemia/Hb E by hemoglobin typing compared to DNA analysis.Interaction between Hb E and Hb Yala (HBB:c.129delT); a novel frameshift beta globin gene mutation, resulting in Hemoglobin E/β0 thalassemia.Genetic determinants of β-thalassemia intermedia in Pakistan.Molecular analysis of beta-thalassemia in South Vietnam.The prevalence and molecular basis of hemoglobinopathies in Cambodia.DOUBLE HETEROZYGOSITY FOR Hb PYRGOS [β83(EF7)Gly→Asp] AND Hb E [β26(B8)Glu→Lys] FOUND IN ASSOCIATION WITH α-THALASSEMIA
P2860
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P2860
Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine.
@en
type
label
Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine.
@en
prefLabel
Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine.
@en
P2860
P1433
P1476
Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine.
@en
P2093
Fucharoen S
Winichagoon P
P2860
P304
P356
10.3109/03630269709000664
P577
1997-07-01T00:00:00Z