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Literature DB >> 24237977

Thalassemias.

Abstract

The thalassemia syndromes are hemoglobin disorders that result from significantly reduced or absent synthesis of either the α- or β-globin chains. The result is a chronic hemolytic anemia with ineffective erythropoiesis and bone marrow overstimulation. This article reviews current diagnostic approaches, complications, and disease management of thalassemia.

Entities: Disease

Keywords: Anemia; Hemoglobinopathies; Iron overload; Thalassemia

Mesh：

Year: 2013 PMID： 24237977 DOI： 10.1016/j.pcl.2013.08.008

Source DB: PubMed Journal: Pediatr Clin North Am ISSN： 0031-3955 Impact factor: 3.278

Keyword Cloud
Cited

23 in total

1. Factor-induced Reprogramming and Zinc Finger Nuclease-aided Gene Targeting Cause Different Genome Instability in β-Thalassemia Induced Pluripotent Stem Cells (iPSCs).

Authors: Ning Ma; Yongli Shan; Baojian Liao; Guanyi Kong; Cheng Wang; Ke Huang; Hui Zhang; Xiujuan Cai; Shubin Chen; Duanqing Pei; Nansheng Chen; Guangjin Pan
Journal: J Biol Chem Date: 2015-03-20 Impact factor: 5.157

2. Computer and mobile technology interventions to promote medication adherence and disease management in people with thalassemia.

Authors: Sherif M Badawy; Kerry Morrone; Alexis Thompson; Tonya M Palermo
Journal: Cochrane Database Syst Rev Date: 2019-06-28

Review 3. The role of iron repletion in adult iron deficiency anemia and other diseases.

Authors: Benjamin Elstrott; Lubna Khan; Sven Olson; Vikram Raghunathan; Thomas DeLoughery; Joseph J Shatzel
Journal: Eur J Haematol Date: 2019-12-26 Impact factor: 2.997

4. Computer and mobile technology interventions to promote medication adherence and disease management in people with thalassemia.

Authors: Sherif M Badawy; Kerry Morrone; Alexis Thompson; Tonya M Palermo
Journal: Cochrane Database Syst Rev Date: 2017-12-14

10. Role of Red Cell Indices in Screening for Beta Thalassemia Trait: an Assessment of the Individual Indices and Application of Machine Learning Algorithm.

Authors: Aarzoo Jahan; Garima Singh; Ruchika Gupta; Namrata Sarin; Sompal Singh
Journal: Indian J Hematol Blood Transfus Date: 2020-10-27 Impact factor: 0.915

Thalassemias.

1. Factor-induced Reprogramming and Zinc Finger Nuclease-aided Gene Targeting Cause Different Genome Instability in β-Thalassemia Induced Pluripotent Stem Cells (iPSCs).

2. Computer and mobile technology interventions to promote medication adherence and disease management in people with thalassemia.

Review 3. The role of iron repletion in adult iron deficiency anemia and other diseases.

4. Computer and mobile technology interventions to promote medication adherence and disease management in people with thalassemia.

5. Splenectomy for people with thalassaemia major or intermedia.

Review 6. A narrative review of in utero gene therapy: advances, challenges, and future considerations.

7. Zinc status affects glucose homeostasis and insulin secretion in patients with thalassemia.

8. Discrimination index of microcytic anemia in young soldiers: a single institutional analysis.

9. Extracellular vesicles in hematological disorders.

10. Role of Red Cell Indices in Screening for Beta Thalassemia Trait: an Assessment of the Individual Indices and Application of Machine Learning Algorithm.