about
Beta-thalassemiaTreatment for osteoporosis in people with ß-thalassaemiaTreatment for osteoporosis in people with ß-thalassaemiaSplenectomy for people with thalassaemia major and intermediaIneffective erythropoiesis and thalassemiasSplenectomy for people with thalassaemia major or intermediaHemoglobin E disorder: Newborn screening programα-thalassaemiaAlpha-thalassemiaGlobal migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000.Effect of breastfeeding versus infant formula on iron status of infants with beta thalassemia major.Atherogenesis and iron: from epidemiology to cellular level.Future alternative therapies for β-thalassemia.Comparative efficacy and safety of deferoxamine, deferiprone and deferasirox on severe thalassemia: a meta-analysis of 16 randomized controlled trials.Nitric oxide and arginine dysregulation: a novel pathway to pulmonary hypertension in hemolytic disordersZinc status affects glucose homeostasis and insulin secretion in patients with thalassemiaβ-Thalassemia and ocular implications: a systematic review.Inadequate dietary intake in patients with thalassemiaThalassemia in the United Arab Emirates: Why it can be prevented but not eradicatedKnowledge, Attitude and Practice of Carrier Thalassemia Marriage Volunteer in Prevention of Major Thalassemia.Clinical Manifestations of β-Thalassemia Major in Two Different Altitudes; Bushehr and ShahrekordRegulation of iron absorption in hemoglobinopathies.Clinical characteristics of pediatric thalassemia in Korea: a single institute experience.Gene therapy in thalassemia and hemoglobinopathies.Deferasirox for the treatment of iron overload in non-transfusion-dependent thalassemia.β-globin genes: mutation hot-spots in the global thalassemia belt.The diminishing trend of β-thalassemia in Southern Iran from 1997 to 2011: the impact of preventive strategies.An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project.Prevalence, Incidence, Trend, and Complications of Thalassemia in Iraq.A Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North Iran.Treating hemoglobinopathies using gene-correction approaches: promises and challenges.Alpha thalassemia allelic frequency in Lebanon.Hydroxyurea for nontransfusion-dependent β-thalassemia: A systematic review and meta-analysis.First Report of a Dominantly Inherited β-Thalassemia Caused by a Novel Elongated β-Globin Chain.[Increase in genetically determined anemia as a result of migration in Germany].Incidence of alpha-globin gene defect in the Lebanese population: a pilot study.Molecular characterisation of Haemoglobin Constant Spring and Haemoglobin Quong Sze with a Combine-Amplification Refractory Mutation System.Early detection of myocardial dysfunction in poorly treated pediatric thalassemia children and adolescents: Two Saudi centers experienceMolecular analysis of beta-globin gene mutations among Thai beta-thalassemia children: results from a single center study.A phase 2 trial of HQK-1001 in HbE-β thalassemia demonstrates HbF induction and reduced anemia.
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-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
2005年學術文章
@zh-hant
name
Changing patterns of thalassemia worldwide.
@ast
Changing patterns of thalassemia worldwide.
@en
type
label
Changing patterns of thalassemia worldwide.
@ast
Changing patterns of thalassemia worldwide.
@en
prefLabel
Changing patterns of thalassemia worldwide.
@ast
Changing patterns of thalassemia worldwide.
@en
P356
P1476
Changing patterns of thalassemia worldwide.
@en
P356
10.1196/ANNALS.1345.003
P407
P577
2005-01-01T00:00:00Z