Pathophysiology and Clinical Manifestations of the β-Thalassemias.
about
Iron deficiency anemia: a common and curable diseaseAn international effort to cure a global health problem: A report on the 19th Hemoglobin Switching Conference.Comparison of various iron chelators and prochelators as protective agents against cardiomyocyte oxidative injury.α-Globin as a molecular target in the treatment of β-thalassemiaThe hemoglobin E thalassemias.Characterization of cytoprotective and toxic properties of iron chelator SIH, prochelator BSIH and their degradation products.Physiology and pathophysiology of iron in hemoglobin-associated diseases.Transcriptional mechanisms underlying hemoglobin synthesis.Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf areaThe search for genetic modifiers of disease severity in the β-hemoglobinopathies.Classification of the disorders of hemoglobinIndividualizing fetal hemoglobin augmenting therapy for β-type hemoglobinopathies patients.Single Breath-Hold Physiotherapy Technique: Effective tool for T2* magnetic resonance imaging in young patients with thalassaemia major.Recent trends in the gene therapy of β-thalassemia.Thalassaemia in children: from quality of care to quality of life.An enhancer haplotype may influence BCL11A expression levels and the response to hydroxyurea in β-thalassemia patients.Deferiprone for the treatment of transfusional iron overload in thalassemia.Fetal hemoglobin regulation in β-thalassemia: heterogeneity, modifiers and therapeutic approaches.First Report of a Dominantly Inherited β-Thalassemia Caused by a Novel Elongated β-Globin Chain.Hypogonadism in thalassemia major patients.Relationship between β-Thalassemia minor and Helicobacter pylori infection.Gonadal dysfunction in adult male patients with thalassemia major: an update for clinicians caring for thalassemia.Correlation of SIN3A genomic variants with β-hemoglobinopathies disease severity and hydroxyurea treatment efficacy.Orphan Drugs and Potential Novel Approaches for Therapies of β-Thalassemia: Current Status and Future Expectations
P2860
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P2860
Pathophysiology and Clinical Manifestations of the β-Thalassemias.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Pathophysiology and Clinical Manifestations of the β-Thalassemias.
@ast
Pathophysiology and Clinical Manifestations of the β-Thalassemias.
@en
type
label
Pathophysiology and Clinical Manifestations of the β-Thalassemias.
@ast
Pathophysiology and Clinical Manifestations of the β-Thalassemias.
@en
prefLabel
Pathophysiology and Clinical Manifestations of the β-Thalassemias.
@ast
Pathophysiology and Clinical Manifestations of the β-Thalassemias.
@en
P2860
P1476
Pathophysiology and Clinical Manifestations of the β-Thalassemias.
@en
P2093
Arthur W Nienhuis
David G Nathan
P2860
P304
P356
10.1101/CSHPERSPECT.A011726
P577
2012-12-01T00:00:00Z