Literature DB >> 22507773

Thalassemia.

Yesim Aydinok1.   

Abstract

Thalassemia is the most common form of inherited anemia worldwide. The World Health Organization reports suggest that about 60,000 infants are born with a major thalassemia every year. Although individuals originating from the tropical belt are most at risk, it is a growing global health problem due to extensive population migrations. Despite important advances on curative approaches such as stem cell transplantation and promising results of gene therapy, blood transfusions and iron chelation still remain as cornerstones of disease management. The purpose of this article is to focus on mainly the clinical aspects and management of beta-thalassemia major.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22507773     DOI: 10.1179/102453312X13336169155295

Source DB:  PubMed          Journal:  Hematology        ISSN: 1024-5332            Impact factor:   2.269


  10 in total

1.  Craniofacial Characteristics of Thalassemia Major Patients.

Authors:  Sacide Karakas; Ayfer Metin Tellioglu; Mehmet Bilgin; Imran Kurt Omurlu; Sercin Caliskan; Salih Coskun
Journal:  Eurasian J Med       Date:  2016-10

Review 2.  Early detection of cardiac involvement in thalassemia: From bench to bedside perspective.

Authors:  Nut Koonrungsesomboon; Siriporn C Chattipakorn; Suthat Fucharoen; Nipon Chattipakorn
Journal:  World J Cardiol       Date:  2013-08-26

3.  Anxiety, depression and quality of life in patients with beta thalassemia major and their caregivers.

Authors:  Erhan Yengil; Can Acipayam; Mehmet Hanifi Kokacya; Faruk Kurhan; Gonul Oktay; Cahit Ozer
Journal:  Int J Clin Exp Med       Date:  2014-08-15

4.  Cardiac T2* MRI assessment in patients with thalassaemia major and its effect on the preference of chelation therapy.

Authors:  Arzu Akcay; Zafer Salcioglu; Kazim Oztarhan; Deniz Tugcu; Gonul Aydogan; Nuray Aktay Ayaz; Helen Bornaun; Hulya Sayilan Sen; Ferhan Akici; Burhan Akdana
Journal:  Int J Hematol       Date:  2014-04-10       Impact factor: 2.490

5.  Epidemiologic Trends of Thalassemia, 2006-2018: A Nationwide Population-Based Study.

Authors:  Jee-Soo Lee; Tae-Min Rhee; Kibum Jeon; Yonggeun Cho; Seung-Woo Lee; Kyung-Do Han; Moon-Woo Seong; Sung-Sup Park; Young Kyung Lee
Journal:  J Clin Med       Date:  2022-04-20       Impact factor: 4.964

6.  Anti-Toxoplasma gondii antibodies in patients with beta-hemoglobinopathies: the first report in the Americas.

Authors:  Marina Neves Ferreira; Claudia Regina Bonini-Domingos; Isabeth Fonseca Estevão; Clarice Lopes de Castro Lobo; Gisele Cristina Souza Carrocini; Aparecida Perpétuo Silveira-Carvalho; Octávio Ricci; Luiz Carlos de Mattos; Cinara Cássia Brandão de Mattos
Journal:  BMC Res Notes       Date:  2017-06-14

7.  Forager and farmer evolutionary adaptations to malaria evidenced by 7000 years of thalassemia in Southeast Asia.

Authors:  Melandri Vlok; Hallie R Buckley; Justyna J Miszkiewicz; Meg M Walker; Kate Domett; Anna Willis; Hiep H Trinh; Tran T Minh; Mai Huong T Nguyen; Lan Cuong Nguyen; Hirofumi Matsumura; Tianyi Wang; Huu T Nghia; Marc F Oxenham
Journal:  Sci Rep       Date:  2021-03-11       Impact factor: 4.379

Review 8.  Prevalence of Depression among Iranian Patients with Beta-Thalassemia Major: A Systematic Review and Meta-analysis.

Authors:  Zahra Jaafari; Nasrin Sadidi; Zahra Abdolahinia; Armita Shahesmaeili
Journal:  Iran J Med Sci       Date:  2022-01

9.  Selenium and Vitamin E as antioxidants in chronic hemolytic anemia: Are they deficient? A case-control study in a group of Egyptian children.

Authors:  Mona M Hamdy; Dalia S Mosallam; Alaa M Jamal; Walaa A Rabie
Journal:  J Adv Res       Date:  2015-01-13       Impact factor: 10.479

Review 10.  Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area.

Authors:  Mohamad H Qari; Yasser Wali; Muneer H Albagshi; Mohammad Alshahrani; Azzah Alzahrani; Ibrahim A Alhijji; Abdulkareem Almomen; Abdullah Aljefri; Hussain H Al Saeed; Shaker Abdullah; Ahmad Al Rustumani; Khoutir Mahour; Shaker A Mousa
Journal:  Orphanet J Rare Dis       Date:  2013-09-17       Impact factor: 4.123

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.