Zobrazeno 1 - 10
of 927
pro vyhledávání: '"β–thalassemia major"'
Autor:
Ammar J. Mohammed, Jabbar H. Yenzeel
Publikováno v:
Ibn Al-Haitham Journal for Pure and Applied Sciences, Vol 37, Iss 4 (2024)
Sixty patients (male and female) with β-thalassemia major and thirty healthy subjects were enrolled in this study during their attendance at "Abin AL-Baladi Hospital in Baghdad" from September 2022 to January 2023. All patients and healthy subjects
Externí odkaz:
https://doaj.org/article/3ffe0e9c8b8c45369cbaf57bd7000550
Publikováno v:
Al-Mustansiriyah Journal of Science, Vol 35, Iss 3 (2024)
Background: Beta-thalassemia is the most prevalent genetic hemoglobin apathy in the world. It is caused by a reduction or absence of beta-globin chain production, which is typically a portion of adult hemoglobin (HbA, which is α2β2). This genetic a
Externí odkaz:
https://doaj.org/article/48b382446d744164b81d8cdeb30fcbb2
Publikováno v:
Acta Scientiarum: Animal Sciences, Vol 46, Iss 1 (2024)
Thalassemia is one of the most important genetic haemolytic diseases that cause the breakdown of red blood cells (RBCs) in patients with β-Thalassemia major. The body does not produce enough haemoglobin, which is an important part of RBCs. When ther
Externí odkaz:
https://doaj.org/article/15588bee5e7f47a0948b032d22c1ca9a
Publikováno v:
Biomolecules & Biomedicine (2024)
Children with severe β-thalassemia major (β-TM) are at high risk of developing toxoplasmosis after allogeneic hematopoietic stem cell transplantation (allo-HSCT). The aim of this study was to identify the neuroimaging findings of cerebral toxoplasm
Externí odkaz:
https://doaj.org/article/6b434b9087e249d99efe539e6678f9df
Autor:
Runqi Zhang, Shuo Zhang, Jing Ming, Jing Xie, Baoguo Liu, Weihang Jiang, Yingjie Fu, Xuemei Zhen, Xiaojie Sun
Publikováno v:
BMC Nursing, Vol 23, Iss 1, Pp 1-10 (2024)
Abstract Background The informal caregivers of adult patients with β-thalassemia major (β-TM) bear not only physical but also emotional and economic pressures of providing care. This study is the first to evaluate the caregiver burden by Zarit Burd
Externí odkaz:
https://doaj.org/article/23e08b6e2adb49e896d977c707cc2298
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss 4, Pp 467-472 (2023)
Introduction: Patients with β-thalassemia major (β-TM) are at risk of developing abnormal lipid profiles. Lipid abnormalities, in turn, have a potential role in the pathogenesis of some clinical aspects of thalassemia Objectives: To evaluate lipid
Externí odkaz:
https://doaj.org/article/4b6666701d6d4ece8049295b329f1540
Autor:
Shahana Khanum, A.N. Thobbi
Publikováno v:
Al Ameen Journal of Medical Sciences, Vol 16, Iss 04, Pp 334-342 (2023)
Objectives: Mean prevalence of thalassemia is nearly 3.5%. Approximately 4% of world’s population is carrier of alpha and beta thalassemia. Cardiac complications are the most common cause of death in β-Thalassemia major. In India, studies regardin
Externí odkaz:
https://doaj.org/article/3b23a8fddbb24a2fac299babc20daf6b
Publikováno v:
Current Issues in Pharmacy and Medical Sciences, Vol 36, Iss 3, Pp 168-173 (2023)
The study’s goal is to appraise the immunological inflammatory marker Trefoil Factor 3, which interacts with thalassemia pathogenesis particularly following splenectomy, and may offer new therapy options for the illness and its repercussions.
Externí odkaz:
https://doaj.org/article/ba82e7b52cf34446b77ff4a61ed0fbd2
Autor:
Hossein Karami, Mehrnoush Kosaryan, Mohammad Naderisorki, Fatemeh esfandiari, Mobin Ghazaiean, Aily Aliasgharian, Hanie Fallah, Salameh Shakeri, Hadi Darvishi-Khezri
Publikováno v:
Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, Vol 31, Iss 6, Pp 6732-6745 (2023)
Introduction: OsteoPenia and osteoPorosis are known to be one of the main comPlications of β-thalassemia major (β-TM). The aim of this study was to determine the factors associated with decreased bone density of these Patients. Methods: Lumbar and
Externí odkaz:
https://doaj.org/article/b8dac6c5fb8d4283af5cca60498c266a
Publikováno v:
Asian Journal of Transfusion Science, Vol 18, Iss 1, Pp 73-78 (2023)
INTRODUCTION: Hepcidin is the key regulator of systemic iron homeostasis. In iron-loading anemias, hepcidin levels are regulated by opposite forces of erythropoiesis and iron overload. In β-thalassemia major patients, transfusions are the predominan
Externí odkaz:
https://doaj.org/article/aa2d4fe3f9ed4c17b09c920c6ce7275f