Zobrazeno 1 - 10
of 1 773
pro vyhledávání: '"Beta thalassemia major"'
Publikováno v:
Paediatrica Indonesiana, Vol 64, Iss 5, Pp 412-8 (2024)
Background Thalassemia is a hemoglobin synthesis disorder that causes patients to need lifelong blood transfusions, leading to iron overload and alter organ function, including the liver. Hepcidin, produced by the liver, plays a role in iron homeosta
Externí odkaz:
https://doaj.org/article/242a93aa783a47a0985f63be85633d26
Autor:
Dhaarani Jayaraman, Harshavardhan Mahalingam, Naga Geetha Rani Mangam, Swati Narasimhan, Padmasani Venkat Ramanan, K. Stephen Sudhakar, Prasanna Kumar S, Banu Keerthana, Manu Vidhya Harikumar, Anupama Jyoti Kindo, T.K. Shruthi, Niranjan Ragavan, Julius Xavier Scott
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 9, Iss 4, Pp 271-273 (2024)
Mucormycosis is a dreaded condition with high mortality rates noted in immunocompromised hosts. Though iron overload is a known risk factor, children with transfusion-dependent thalassemia have been rarely reported with invasive mucormycosis. We pres
Externí odkaz:
https://doaj.org/article/71d6728ce30049ccb09aebd14e25de29
Autor:
Sameh M. Nahi, Ferdous A. Jabir
Publikováno v:
Journal of Applied Hematology, Vol 15, Iss 3, Pp 185-191 (2024)
Background: Thalassemia is an inherited disorder that is also called mediterranean anemia and is described by a lack of hemoglobin synthesis. β-thalassemia is more common in people of certain origins, particularly those from the Mediterranean region
Externí odkaz:
https://doaj.org/article/a464c96331744d8b9a9a3c8557e7d26a
Autor:
Hossein Jalali, Mohammad Reza Mahdavi, Mehrnoush Kosaryan, Ahmad Najafi, Aily Aliasgharian, Ebrahim Salehifar
Publikováno v:
Thalassemia Reports, Vol 14, Iss 3, Pp 71-80 (2024)
HbF induction is an appropriate strategy to ameliorate the severity of β-thalassemia symptoms. Hydroxyurea (HU) is the most common chemical agent introduced as an HbF inducer but responsiveness to HU is variable and the introduction of HbF inducers
Externí odkaz:
https://doaj.org/article/28040da465084f7b966b7a8289701c21
Autor:
Shaima’A Dakhel ABDULHASSAN
Publikováno v:
Modern Medicine, Vol 31, Iss 3, Pp 221-226 (2024)
Introduction: Thalassemia, a hereditary autosomal recessive blood disorder, arises from genetic abnormalities leading to a diminished synthesis rate of one of the globin chains constituting hemoglobin. The integration of transfusion and chelation the
Externí odkaz:
https://doaj.org/article/282b8dd2bd024a5fa176c680948a83c8
Publikováno v:
Armaghane Danesh Bimonthly Journal, Vol 29, Iss 4, Pp 482-496 (2024)
Background & aim: Thalassemia major is a chronic genetic blood disease. This disease causes fatigue in people and affects different aspects of their lives, therefore the purpose of the present study was to determine the effect of intervention based o
Externí odkaz:
https://doaj.org/article/aa7c06ab107e4d3aa7926db7e3704893
Publikováno v:
Archives of Medicine and Health Sciences, Vol 12, Iss 1, Pp 44-48 (2024)
Background and Aim: Kidney dysfunction is reported in significant number of beta thalassemia major children. The aim of this study was to determine the prevalence of glomerular dysfunction in beta-thalassemia major children on regular blood transfusi
Externí odkaz:
https://doaj.org/article/551a4421ad38454897633bb66e9a8956
Publikováno v:
Guoji Yanke Zazhi, Vol 24, Iss 4, Pp 601-606 (2024)
Beta-thalassemia major(β-TM)is an inherited disease caused by a defect in the synthesis of globin. The disease requires long-term blood transfusion and iron chelator treatment, which can cause various secondary changes in the body and eye tissues. C
Externí odkaz:
https://doaj.org/article/b9a9bc24d7744683b208c1ebf67f5248
Publikováno v:
Journal of Kerman University of Medical Sciences, Vol 31, Iss 1, Pp 46-50 (2024)
Background: Cardiac iron overload causes severe cardiac complications and is a leading cause of death in beta-thalassemia major patient. T2*CMR can detect preclinical cardiac iron overload. We evaluated the ability of 12-lead electrocardiographic atr
Externí odkaz:
https://doaj.org/article/30a9221ce6a24709b7f9c1318ab13996
Publikováno v:
Advances in Rehabilitation, Vol 38, Iss 1, Pp 1-8 (2024)
Externí odkaz:
https://doaj.org/article/f3dcc29ce5cc44ea85872e4fcd16357b