Zobrazeno 1 - 10
of 5 377
pro vyhledávání: '"Thalassemia major"'
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
Autor:
Ahmed I. Ansaf, Alaa M. Al-Rubae, Taghreed S. Saeed Al-Rawi, Sarah A. Najem, Hamasat J. Ali, Safa A. Faraj, Raid M. Al-Ani
Publikováno v:
Journal of Applied Hematology, Vol 15, Iss 2, Pp 116-120 (2024)
BACKGROUND: Despite prolonged life expectancy in patients with beta-thalassemia due to modern chelation therapy and planned blood transfusions, they still suffer from multisystem complications of this chronic hemolytic anemia, including endocrine sys
Externí odkaz:
https://doaj.org/article/66bc0ebee8bd4727ab80ec33b38b9dd0
Publikováno v:
Journal of Applied Hematology, Vol 15, Iss 2, Pp 121-129 (2024)
BACKGROUND: Alloantibodies against donor red blood cells (RBCs) are developed by patients with transfusion-dependent thalassemia (TDT), which causes the donor RBCs to hemolyze. This decreases the transfusion’s efficacy and increases the risk of adv
Externí odkaz:
https://doaj.org/article/70ca61b9c53347c3a7338924465bdc60
Autor:
Teny Tjitra Sari, Ludi Dhyani Rahmartani, Angga Wirahmadi, Nathasha Brigitta Selene, Stephen Diah Iskandar, Pustika Amalia Wahidiyat
Publikováno v:
Thalassemia Reports, Vol 14, Iss 2, Pp 33-43 (2024)
Thalassemia a common hereditary blood disorder resulting in anemia. It is an important public health problem, with a high prevalence in Southeast Asia and Mediterranean countries, and preventable through screening programs. However, due to its chroni
Externí odkaz:
https://doaj.org/article/ef6c855ba45041adbb867ba73db80bcc
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
Autor:
Laleh Hassani, Niloofar Seyrafi, Sama Mohammadi, Teamur Aghamolaei, Amin Ghanbarnejad, Mohammad Reza Evazi
Publikováno v:
Health Science Reports, Vol 7, Iss 9, Pp n/a-n/a (2024)
Abstract Background and Aim Due to the adverse effects of their disease, patients with thalassemia major face many problems such as a lack of proper growth, enlarged spleen and liver, bone disorders, especially the bones of the head and face. As a re
Externí odkaz:
https://doaj.org/article/59548d7c1a624a55a326f52167aeb207
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
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