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Titlebook: Radiology of Thalassemia; Constantin Papavasiliou,Theophanis Cambouris,Phaed Book 1989 Springer-Verlag Berlin Heidelberg 1989 bone.bone ma

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书目名称Radiology of Thalassemia
编辑Constantin Papavasiliou,Theophanis Cambouris,Phaed
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图书封面Titlebook: Radiology of Thalassemia;  Constantin Papavasiliou,Theophanis Cambouris,Phaed Book 1989 Springer-Verlag Berlin Heidelberg 1989 bone.bone ma
描述Estimates reveal that there are some 200 million heterozygous carriers of abnormal hemoglobins genes worldwide, and tens of thousands of severely affected patients. Effective application of imaging techniques is essential to combat the continuing development of the disease and to ensure risk-free follow-up of the chronically ill. This is the first book to offer complete coverage of such radiologic applications with both conventional and the most modern imaging modalities. Interventional radiology, marrow transplantation, prenatal diagnosis by ultrasonography, and radiotherapy for bone marrow heterotopia are also featured.
出版日期Book 1989
关键词bone; bone marrow; diagnosis; genes; interventional radiology; prenatal diagnosis; radiology; radiotherapy;
版次1
doihttps://doi.org/10.1007/978-3-642-72587-6
isbn_softcover978-3-642-72589-0
isbn_ebook978-3-642-72587-6
copyrightSpringer-Verlag Berlin Heidelberg 1989
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Grading System of Osseous Changes in ThalassemiaThe radiological changes encountered in thalassemia and its variants involve many organs. There is general agreement to group these changes into two main categories: osseous and extraosseous manifestations.
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Computed Tomography Evaluation of the Upper Abdomen in ,-ThalassemiaClinical management of .-thalassemia depends on repeated blood transfusions and on chelation therapy. Computed tomography (CT) can provide the opportunity to relate CT density to iron deposition; therefore, CT appearance may be essential for evaluation of abdominal organs for the degree of hemochromatosis.
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Abdominal Ultrasonography in ,-ThalassemiaChildren with .-thalassemia transfused and followed up regularly are prone to develop symptoms of iron overload early in life. Parenchymal iron loading, largely in the form of ferritin, results in widespread hemosiderosis, responsible for tissue damage in most of the abdominal organs.
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978-3-642-72589-0Springer-Verlag Berlin Heidelberg 1989
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Introductionarated this syndrome from other cases of childhood anemia, thalassemia has risen gradually to an unparalleled prominence. The disease has existed with us over many millenia, if the paleo-anthropological evidence obtained from excavated skulls is being interpreted correctly.
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Bone Marrow Transplantation for Thalassemia Major: The Place of Irradiationuces or prevents hemosiderosis caused by this form of therapy. With this conventional treatment, life expectancy may exceed more than 25 years, and many patients manage to maintain normal activity and, occasionally, to raise families.
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https://doi.org/10.1007/978-3-642-72587-6bone; bone marrow; diagnosis; genes; interventional radiology; prenatal diagnosis; radiology; radiotherapy;
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