Zobrazeno 1 - 10
of 209
pro vyhledávání: '"Beta thalassaemia major"'
Publikováno v:
Journal of Clinical and Scientific Research, Vol 12, Iss 5, Pp 48-52 (2023)
Background: Chronic blood disorders such as beta-thalassaemia major require continuous blood transfusions, which results in complications such as transfusion-transmitted infections (TTIs), iron overload, skeletal deformities, endocrinal and cardiac a
Externí odkaz:
https://doaj.org/article/09109ac558ba4b779fb230e491272b0d
Autor:
Jianyun Wen, Xiaodong Wang, Libai Chen, Yuelin He, Xiaoqin Feng, Chunfu Li, Yongshen Ruan, Sixi Liu, Xuedong Wu
Publikováno v:
Hematology, Vol 27, Iss 1, Pp 310-317 (2022)
Background Allogeneic haematopoietic stem cell transplantation (allo-HSCT) is currently the only curative treatment for thalassaemia major (TM). Cord blood (CB) from a sibling has different characteristics from marrow and has potential advantages and
Externí odkaz:
https://doaj.org/article/98e6594769f14e3a9ccab826f116de9e
Publikováno v:
Health and Quality of Life Outcomes, Vol 18, Iss 1, Pp 1-8 (2020)
Abstract Background Beta Thalassaemia Major (βTM) is a chronic genetic illness whereby the challenges faced by patients exposes them to increased risk of psychosocial issues. Despite this, a disease-specific tool to measure the impact of this illnes
Externí odkaz:
https://doaj.org/article/46205198222b4fa6a51c60a4311557b0
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 4, Pp SC01-SC07 (2018)
Introduction: Iron-mediated cardiomyopathy is leading cause of death in β-thalassaemia (βTM). Thyroid dysfunction maybe associated with cardiac dysfunctions. Early detection of cardiacfunction impairment can help in preventing further cardiac damag
Externí odkaz:
https://doaj.org/article/211f2df1a4fc45bfa831ce9b2f26cf70
Autor:
Sundas Ali
Publikováno v:
Journal of Rawalpindi Medical College, Vol 21, Iss 3 (2017)
To assess the attitudes and practices of parents of Beta-Thalassaemia Major children regarding Chorionic Villous Sampling (CVS), as prenatal diagnosis in subsequent pregnancies. Methods: In this cross-sectional study a pre-designed questionnaire was
Externí odkaz:
https://doaj.org/article/e84cb8b7b0894e5c8eb4925aecea23fe
Publikováno v:
Acta Cardiologica. 77:71-80
To evaluate the utility of cardiac magnetic resonance feature tracking-derived left ventricular strain in assessing cardiac dysfunction and investigate the correlation between left ventricular strain and myocardial T2* in patients with beta-thalassae
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0ecd8d1be71d6faff4451477a0d29f4
https://doi.org/10.1080/00015385.2021.1887585
https://doi.org/10.1080/00015385.2021.1887585
Publikováno v:
BioImpacts, Vol 11, Iss 2, Pp 129-133 (2021)
BioImpacts : BI
BioImpacts : BI
Introduction: Thalassemia is associated with a genetic decline in the rate of synthesis of one or more types of natural hemoglobin polypeptide chains. One of the major complications in thalassemia patients is alloimmunization, which is antibody produ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c143206d70a1a36778a49fff82d1e90
https://bi.tbzmed.ac.ir/PDF/bi-11-129.pdf
https://bi.tbzmed.ac.ir/PDF/bi-11-129.pdf
Akademický článek
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Akademický článek
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Autor:
Madeeha Rehan
Publikováno v:
Journal of Rawalpindi Medical College, Vol 19, Iss 2 (2015)
Background: To study the frequency and specificity of various red cell alloantibodies in multi- transfused patients of beta thalassaemia major. Methods: In this comparative study two hundred diagnosed cases of Beta Thalassemia Major , of all ages and
Externí odkaz:
https://doaj.org/article/bcb3fcdbf7a448cab7215737f68eb63a