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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 1
1982 1
1983 1
1987 1
1988 2
1991 2
1993 3
1996 1
1997 2
1998 2
1999 1
2000 4
2001 2
2002 1
2003 1
2004 1
2005 2
2006 1
2007 1
2008 7
2009 4
2010 5
2011 3
2012 6
2013 9
2014 3
2015 4
2016 5
2017 6
2018 4
2019 7
2020 4
2021 8
2022 6
2023 6
2024 0

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105 results

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Page 1
Prevalence and Management of beta-Thalassemia in India.
Yadav SS, Panchal P, Menon KC. Yadav SS, et al. Hemoglobin. 2022 Jan;46(1):27-32. doi: 10.1080/03630269.2021.2001346. Epub 2022 Feb 7. Hemoglobin. 2022. PMID: 35129043 Review.
India bears a huge burden of hemoglobinopathies, and the most prevalent is thalassemia. The different types of thalassemia include minor, major and intermedia, based on the alpha/beta-globin chain inequality. This review aimed to understand the current …
India bears a huge burden of hemoglobinopathies, and the most prevalent is thalassemia. The different types of thalassemia inc …
Thalassemia: Common Clinical Queries in Management.
Lal A, Bansal D. Lal A, et al. Indian J Pediatr. 2020 Jan;87(1):75-81. doi: 10.1007/s12098-019-03065-5. Epub 2019 Oct 16. Indian J Pediatr. 2020. PMID: 31620986 Review.
Beta thalassemia major (TM) is the most frequent form of transfusion-dependent inherited anemia in India. ...Among the topics under discussion are deciding when to start regular transfusions, the role of hydroxyurea in TM, the procedure for blood administrati …
Beta thalassemia major (TM) is the most frequent form of transfusion-dependent inherited anemia in India. ...Among the …
Prevention programmes and prenatal diagnosis for beta thalassemia in Pakistan: A narrative review.
Ghafoor M, Sabar MF, Sabir F. Ghafoor M, et al. J Pak Med Assoc. 2021 Jan;71(1(B)):326-331. doi: 10.47391/JPMA.665. J Pak Med Assoc. 2021. PMID: 35157672 Free article. Review.
Beta thalassemia in Pakistan is a serious health concern with an estimated 5-8% carrier frequency and birth of 5000 major children every year in the country. The treatment of beta thalassemia major patients poses a great economic burden; …
Beta thalassemia in Pakistan is a serious health concern with an estimated 5-8% carrier frequency and birth of 5000 major …
The ethics of genetic screening for beta thalassemia in Vietnam.
Riquier MT. Riquier MT. Dev World Bioeth. 2022 Mar;22(1):44-52. doi: 10.1111/dewb.12316. Epub 2021 May 11. Dev World Bioeth. 2022. PMID: 33974342
In this paper, I argue that genetic screening for beta thalassemia major is ethically justified in the context of Vietnam. ...To lay the groundwork for ethical discussion, I explain the basics of beta thalassemia biochemistry and screening and t …
In this paper, I argue that genetic screening for beta thalassemia major is ethically justified in the context of Vietn …
Atrial fibrillation in beta-thalassemia Major Patients: Diagnosis, Management and Therapeutic Options.
Barbero U, Fornari F, Guarguagli S, Gaglioti CM, Longo F, Doronzo B, Anselmino M, Piga A. Barbero U, et al. Hemoglobin. 2018 May;42(3):189-193. doi: 10.1080/03630269.2018.1488724. Epub 2018 Oct 1. Hemoglobin. 2018. PMID: 30270686 Free article. Review.
The prevalence of atrial fibrillation (AFib) in beta-thalassemia major (beta-TM) patients has increased in the last few years, reaching up to 33.0%. Several factors may drive this value to even more in the next few years. We summarized the main challen …
The prevalence of atrial fibrillation (AFib) in beta-thalassemia major (beta-TM) patients has increased in the l …
Electrocardiographic Presentation, Cardiac Arrhythmias, and Their Management in beta-Thalassemia Major Patients.
Russo V, Rago A, Papa AA, Nigro G. Russo V, et al. Ann Noninvasive Electrocardiol. 2016 Jul;21(4):335-42. doi: 10.1111/anec.12389. Epub 2016 Jun 20. Ann Noninvasive Electrocardiol. 2016. PMID: 27324981 Free PMC article. Review.
Beta-thalassemia major (beta-TM) is a genetic hemoglobin disorder characterized by an absent synthesis of globin chains that are essential for hemoglobin formation, causing chronic hemolytic anemia. ...Heart failure and arrhythmias, caused by myocardia …
Beta-thalassemia major (beta-TM) is a genetic hemoglobin disorder characterized by an absent synthesis of globin …
Clinical management of beta-thalassemia major.
Wonke B. Wonke B. Semin Hematol. 2001 Oct;38(4):350-9. doi: 10.1016/s0037-1963(01)90029-0. Semin Hematol. 2001. PMID: 11605170 Review.
Management of patients with beta-thalassemia is based on adequate, safe blood transfusions (free of transfusion-transmitted diseases) and prevention of iron overload. ...With the emergence of the advanced cardiac magnetic resonance imaging technique, early diagnosis …
Management of patients with beta-thalassemia is based on adequate, safe blood transfusions (free of transfusion-transmitted di …
Cardiac involvement in beta-thalassaemia: current treatment strategies.
Paul A, Thomson VS, Refat M, Al-Rawahi B, Taher A, Nadar SK. Paul A, et al. Postgrad Med. 2019 May;131(4):261-267. doi: 10.1080/00325481.2019.1608071. Epub 2019 May 6. Postgrad Med. 2019. PMID: 31002266 Review.
Despite the advances in the management of thalassemia major, heart disease remains the leading cause of mortality in patients afflicted with this disorder. ...In this review, we look at the pathogenesis of cardiac involvement in patients with beta-thalasse …
Despite the advances in the management of thalassemia major, heart disease remains the leading cause of mortality in patients …
Increasing prevalence of thalassemia in America: Implications for primary care.
Sayani FA, Kwiatkowski JL. Sayani FA, et al. Ann Med. 2015;47(7):592-604. doi: 10.3109/07853890.2015.1091942. Epub 2015 Nov 5. Ann Med. 2015. PMID: 26541064 Review.
Early carrier screening in at-risk populations can help clinicians implement genetic counseling and prevent new cases. Chronic transfusions are the mainstay of therapy for patients with severe thalassemia (beta thalassemia major), and are used i …
Early carrier screening in at-risk populations can help clinicians implement genetic counseling and prevent new cases. Chronic transfusions …
Approach to the management of beta thalassemia major associated osteoporosis - A long-standing relationship revisited.
Yavropoulou MP, Anastasilakis AD, Tzoulis P, Tournis S, Rigatou E, Kassi E, Kattamis A, Makras P. Yavropoulou MP, et al. Acta Biomed. 2022 Oct 26;93(5):e2022305. doi: 10.23750/abm.v93i5.13668. Acta Biomed. 2022. PMID: 36300213 Free PMC article. Review.
Adults with beta- thalassemia major (beta-TM) develop low BMD and fragility fractures at a higher incidence and at a younger age compared to the general population. ...Considering the unique characteristics of osteoporosis associated with beta-T …
Adults with beta- thalassemia major (beta-TM) develop low BMD and fragility fractures at a higher incidence and …
105 results