BackgroundPatients with thalassemia major (Thal) frequently have low plasma zinc, which has been associated with low bone mass.ObjectiveThe objective was to determine the effect of zinc supplementation on bone mass in patients with Thal.DesignForty-two subjects (21 females aged 10-30 y) with Thal and low bone mass were randomly assigned to receive 25 mg Zn/d or placebo. Bone mineral content (BMC) and areal bone mineral density (aBMD) were assessed by using dual-energy X-ray absorptiometry, and fasting blood was collected for the measurement of plasma zinc at 0, 12, and 18 mo.ResultsThirty-two subjects, 81% of whom were transfusion dependent, completed the study (mean ± SD: 17.1 ± 5.2 y). Plasma zinc was ≤70 μg/dL in 11 subjects at baseline ...
Background: Measurements of copper and zinc in transfusion-dependent thalassemia (TDT) show contradi...
The authors investigated the prevalence of low bone mass in patients from Tehran, Iran, with β-thal...
Abstract Background: Beta-thalassemia is an autosomal recessive hemoglobinopathy with frequent skel...
Background: Patients with thalassemia major (Thal) frequently have low plasma zinc, which has been a...
Zinc is one of the essential micronutrients in human and act as a cofactor for more than 300 enzymes...
BACKGROUND: Zinc is one of the most important minerals incorporated in the enzymes of the human body...
Management of thalassemia major has shown substantial clinical and prognostic improvement, suggestin...
Objective: The main purpose of this research work is to compare the levels of serum zinc among the p...
Introduction: In case of zinc (Zn) deficiency, this mineral becomes a nutrient limiting muscle and b...
Objective: This research work carried out to provide the comparison of level of serum zinc between t...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happen...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happens...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happens...
Objective: There are some reports in which a condition of zinc deficiency and its associated outcom...
Zinc (Zn) is essential for appropriate growth and proper immune function, both of which may be impai...
Background: Measurements of copper and zinc in transfusion-dependent thalassemia (TDT) show contradi...
The authors investigated the prevalence of low bone mass in patients from Tehran, Iran, with β-thal...
Abstract Background: Beta-thalassemia is an autosomal recessive hemoglobinopathy with frequent skel...
Background: Patients with thalassemia major (Thal) frequently have low plasma zinc, which has been a...
Zinc is one of the essential micronutrients in human and act as a cofactor for more than 300 enzymes...
BACKGROUND: Zinc is one of the most important minerals incorporated in the enzymes of the human body...
Management of thalassemia major has shown substantial clinical and prognostic improvement, suggestin...
Objective: The main purpose of this research work is to compare the levels of serum zinc among the p...
Introduction: In case of zinc (Zn) deficiency, this mineral becomes a nutrient limiting muscle and b...
Objective: This research work carried out to provide the comparison of level of serum zinc between t...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happen...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happens...
Objective: In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happens...
Objective: There are some reports in which a condition of zinc deficiency and its associated outcom...
Zinc (Zn) is essential for appropriate growth and proper immune function, both of which may be impai...
Background: Measurements of copper and zinc in transfusion-dependent thalassemia (TDT) show contradi...
The authors investigated the prevalence of low bone mass in patients from Tehran, Iran, with β-thal...
Abstract Background: Beta-thalassemia is an autosomal recessive hemoglobinopathy with frequent skel...