about
Hb E/beta-thalassaemia: a common & clinically diverse disorderWhen to consider transfusion therapy for patients with non-transfusion-dependent thalassaemia.Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait.Phosphoproteomic analysis of apoptotic hematopoietic stem cells from hemoglobin E/β-thalassemia.A functional element necessary for fetal hemoglobin silencingHaemoglobinopathies in southeast Asia.α-Globin as a molecular target in the treatment of β-thalassemiaAge-related changes in adaptation to severe anemia in childhood in developing countriesThe hemoglobin E thalassemias.HbE/β-Thalassemia and Oxidative Stress: The Key to Pathophysiological Mechanisms and Novel Therapeutics.Methemoglobinemia and ascorbate deficiency in hemoglobin E β thalassemia: metabolic and clinical implications.The switch from fetal to adult hemoglobinNon-transfusion-dependent thalassemias.Regulation of the fetal hemoglobin silencing factor BCL11A.Interaction of malaria with a common form of severe thalassemia in an Asian population.Iron overload across the spectrum of non-transfusion-dependent thalassaemias: role of erythropoiesis, splenectomy and transfusions.Advances in the understanding of haemoglobin switching.Modifier genes in Mendelian disorders: the example of hemoglobin disorders.Understanding α-globin gene regulation and implications for the treatment of β-thalassemia.Laboratory diagnosis of thalassemia.Target-based drug discovery for [Formula: see text]-globin disorders: drug target prediction using quantitative modeling with hybrid functional Petri nets.Hb E-β-Thalassemia in Five Indian States.Hemoglobin E Hemoglobinopathy in an Adult from Assam with Unusual Presentation: A Diagnostic Dilemma.Selective silencing of α-globin by the histone demethylase inhibitor IOX1: a potentially new pathway for treatment of β-thalassemia.Is hemoglobin e gene widely spread in the state of madhya pradesh in central India? Evidence from five typical families.High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh.Prevalence and risk factors for pulmonary hypertension in patients with hemoglobin E/β-thalassemia disease.Prenatal Diagnosis of HbE-β-Thalassemia: Experience of a Center in Western India
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh-hant
name
Haemoglobin E beta thalassaemia in Sri Lanka.
@en
Haemoglobin E beta thalassaemia in Sri Lanka.
@nl
type
label
Haemoglobin E beta thalassaemia in Sri Lanka.
@en
Haemoglobin E beta thalassaemia in Sri Lanka.
@nl
prefLabel
Haemoglobin E beta thalassaemia in Sri Lanka.
@en
Haemoglobin E beta thalassaemia in Sri Lanka.
@nl
P2093
P1433
P1476
Haemoglobin E beta thalassaemia in Sri Lanka
@en
P2093
A O'Donnell
A Premawardhena
C A Fisher
D J Weatherall
M Arambepola
N F Olivieri
S de Silva
T E A Peto
V Viprakasit
P304
P356
10.1016/S0140-6736(05)67396-5
P407
P577
2005-10-01T00:00:00Z