Iron overload cardiomyopathy: using the latest evidence to inform future applications
S Kumfu, SC Chattipakorn… - … Biology and Medicine, 2022 - journals.sagepub.com
Iron overload can be the result of either dysregulated iron metabolism in the case of
hereditary hemochromatosis or repeated blood transfusions in the case of secondary …
hereditary hemochromatosis or repeated blood transfusions in the case of secondary …
Zinc supplementation and cardiovascular disease risk factors: A GRADE-assessed systematic review and dose-response meta-analysis
M Nazari, D Ashtary-Larky, M Nikbaf-Shandiz… - Journal of Trace …, 2023 - Elsevier
Background and objective A deficit in zinc has been related to a higher probability of
developing cardiovascular diseases (CVDs). The anti-inflammatory and anti-oxidative …
developing cardiovascular diseases (CVDs). The anti-inflammatory and anti-oxidative …
Benefits of curcumin supplementation on antioxidant status in β-Thalassemia major patients: A double-blind randomized controlled clinical trial
E Nasseri, E Mohammadi, A Tamaddoni… - Annals of Nutrition and …, 2018 - karger.com
Background: β-Thalassemia major, the most common inherited anemia in the world, is
associated with imbalance in the oxidant-antioxidant system. The objective of this study was …
associated with imbalance in the oxidant-antioxidant system. The objective of this study was …
Clinical efficacy of zinc supplementation in improving antioxidant defense system: A comprehensive systematic review and time-response meta-analysis of controlled …
Oxidative stress is a contributing factor to many chronic diseases. It has been investigated
that zinc (Zn) may enhance the antioxidant defense. The current dose-response and time …
that zinc (Zn) may enhance the antioxidant defense. The current dose-response and time …
[HTML][HTML] Silibinin: an old drug for hematological disorders
H Zou, XX Zhu, GB Zhang, Y Ma, Y Wu, DS Huang - Oncotarget, 2017 - ncbi.nlm.nih.gov
ABSTRACT Introduction: Silibinin (silybin), a non-toxic natural polyphenolic flavonoid, is the
principal and the most biologically active component of silymarin. It is efficient in the …
principal and the most biologically active component of silymarin. It is efficient in the …
Zinc supplements for treating thalassaemia and sickle cell disease
KMM Swe, ABL Abas, A Bhardwaj… - Cochrane Database …, 2013 - cochranelibrary.com
Background Haemoglobinopathies, inherited disorders of haemoglobin synthesis
(thalassaemia) or structure (sickle cell disease), are responsible for significant morbidity and …
(thalassaemia) or structure (sickle cell disease), are responsible for significant morbidity and …
[HTML][HTML] Nutritional studies in patients with β-thalassemia major: A short review
Background: Patients with β-thalassemia major (BTM) had variable prevalence of
undernutrition and abnormal body composition. Methods: We performed an electronic …
undernutrition and abnormal body composition. Methods: We performed an electronic …
The potential hepatoprotective effect of metformin in hepatitis C virus‐infected adolescent patients with beta thalassemia major: Randomised clinical trial
MS Abdel Monem, SF Farid… - … Journal of Clinical …, 2021 - Wiley Online Library
Background Iron overload‐induced oxidative stress and transfusion‐acquired hepatitis C
virus (HCV) infection are the main reasons of liver damage in beta thalassemia major (β …
virus (HCV) infection are the main reasons of liver damage in beta thalassemia major (β …
Bone-related complications of transfusion-dependent beta thalassemia among children and adolescents
NZ Mirhosseini, S Shahar… - Journal of bone and …, 2013 - Springer
Thalassemia and the blood transfusion complications associated with it predispose children
to poor bone health. This study was conducted to determine the prevalence of bone-related …
to poor bone health. This study was conducted to determine the prevalence of bone-related …
Evaluating the safety and efficacy of silymarin in β-thalassemia patients: a review
BAS Moayedi Esfahani, N Reisi, M Mirmoghtadaei - Hemoglobin, 2015 - Taylor & Francis
Abstract β-Thalassemia (β-thal) is a type of hereditary anemia affecting hemoglobin (Hb)
synthesis causing severe chronic anemia in homozygous patients. Regular blood …
synthesis causing severe chronic anemia in homozygous patients. Regular blood …