Cargando…
Hematological and biochemical status of Beta-thalassemia major patients in Bangladesh: A comparative analysis
Background: Thalassemia is one of the most common hereditary disorders and Beta-thalassemia major is its severe form. The present study is concerned with the analysis of liver function, thyroid function and estimation of critical serum ions as well as hematological characteristics in beta-thalassemi...
Autores principales: | Karim, Md. Fazlul, Ismail, Md., Hasan, AKM Mahbub, Shekhar, Hossain Uddin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818791/ https://www.ncbi.nlm.nih.gov/pubmed/27047645 |
Ejemplares similares
-
Respiratory Burst Enzymes, Pro-Oxidants and Antioxidants Status in Bangladeshi Population with β-Thalassemia Major
por: Hossain, Md. Faruk, et al.
Publicado: (2015) -
Pattern of β-Thalassemia and Other Haemoglobinopathies: A Cross-Sectional Study in Bangladesh
por: Uddin, M. Mesbah, et al.
Publicado: (2012) -
Comment on: oxidative stress and antioxidant status in beta-thalassemia
heterozygotes
por: Shekhar, Hossain Uddin
Publicado: (2013) -
Impaired acylcarnitine profile in transfusion-dependent beta-thalassemia major patients in Bangladesh
por: Kumar Sarker, Suprovath, et al.
Publicado: (2018) -
Correlation of Oxidative Stress with Serum Trace Element Levels and Antioxidant Enzyme Status in Beta Thalassemia Major Patients: A Review of the Literature
por: Shazia, Q., et al.
Publicado: (2012)