about
Hydroxyurea for ß-thalassaemia majorFrequency of Celiac Disease in Children with Beta Thalassemia major.Non-invasive haemoglobin estimation in patients with thalassaemia major.Guidelines for the Standard Monitoring of Patients With Thalassemia: Report of the Thalassemia Longitudinal Cohort.Risk of erectile dysfunction in transfusion-naive thalassemia men: a nationwide population-based retrospective cohort studySurgical outcome of spelenectomy in Thalassemia major in children.Chronic Iron Overload Results in Impaired Bacterial Killing of THP-1 Derived Macrophage through the Inhibition of Lysosomal AcidificationHealth-Related Quality of Life and Health Utility Values in Beta Thalassemia Major Patients Receiving Different Types of Iron Chelators in Iran.Frequency of glomerular dysfunction in children with Beta thalassaemia majorSerum YKL-40 levels and chitotriosidase activity in patients with beta-thalassemia major.Alternative options for DNA-based experimental therapy of β-thalassemia.Pleiotropic actions of iron balance in diabetes mellitus.The importance of nutrition for health in patients with transfusion-dependent thalassemia.Management of iron overload in hemoglobinopathies: what is the appropriate target iron level?The Prevalence of α-Thalassemia and Its Relation to Plasmodium falciparum Infection in Patients Presenting to Clinics in Two Distinct Ecological Zones in Ghana.Benefits of Curcumin Supplementation on Antioxidant Status in β-Thalassemia Major Patients: A Double-Blind Randomized Controlled Clinical Trial.Pulmonary dysfunction in thalassaemia major: is there any relationship with body iron stores?Hydroxyurea responsiveness in β-thalassemic patients is determined by the stress response adaptation of erythroid progenitors and their differentiation propensity.Health-Related Quality of Life in Adolescents with Thalassemia.Combining gene therapy and fetal hemoglobin induction for treatment of β-thalassemia.Is the Benefit-Risk Ratio for Patients with Transfusion-Dependent Thalassemia Treated by Unrelated Cord Blood Transplantation Favorable?Retinal nerve fiber layer thickness in children with β-thalassemia major.Adrenal insufficiency: An emerging challenge in thalassemia?A randomized, controlled study evaluating effects of amlodipine addition to chelators to reduce iron loading in patients with thalassemia major.Exploring Iranian β-Thalassemia major patients' perception of barriers and facilitators of adherence to treatment: A qualitative study.Orphan Drugs and Potential Novel Approaches for Therapies of β-Thalassemia: Current Status and Future ExpectationsQuantification of HBG mRNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta-thalassemia.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on June 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Complications of thalassemia major and their treatment.
@en
Complications of thalassemia major and their treatment.
@nl
type
label
Complications of thalassemia major and their treatment.
@en
Complications of thalassemia major and their treatment.
@nl
prefLabel
Complications of thalassemia major and their treatment.
@en
Complications of thalassemia major and their treatment.
@nl
P2860
P356
P1476
Complications of thalassemia major and their treatment.
@en
P2093
Caterina Borgna-Pignatti
Maria Rita Gamberini
P2860
P304
P356
10.1586/EHM.11.29
P577
2011-06-01T00:00:00Z