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- W1967676619 endingPage "9" @default.
- W1967676619 startingPage "1" @default.
- W1967676619 abstract "Thalassemia intermedia (TI), also known as nontransfusion dependent thalassemia (NTDT), is a type of thalassemia where affected patients do not require lifelong regular transfusions for survival but may require occasional or even frequent transfusions in certain clinical settings and for defined periods of time. NTDT encompasses three distinct clinical forms: β -thalassemia intermedia ( β -TI), Hb E/ β -thalassemia, and α -thalassemia intermedia (Hb H disease). Over the past decade, our understanding of the molecular features, pathophysiology, and complications of NTDT particularly β -TI has increased tremendously but data on optimal treatment of disease and its various complications are still lacking. In this paper, we shall review a group of commonly encountered complications in β -TI, mainly endocrine and bone complications." @default.
- W1967676619 created "2016-06-24" @default.
- W1967676619 creator A5008439187 @default.
- W1967676619 creator A5021368239 @default.
- W1967676619 creator A5022979183 @default.
- W1967676619 creator A5074807429 @default.
- W1967676619 date "2015-01-01" @default.
- W1967676619 modified "2023-09-26" @default.
- W1967676619 title "Endocrine and Bone Complications in<i>β</i>-Thalassemia Intermedia: Current Understanding and Treatment" @default.
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