LIEN
发表于 2025-3-23 13:42:57
A Reappraisal of Some Skeletal Changes in Currently Treated ,-Thalassemiaal skeleton, where the bone marrow remains red. Therefore, in adolescence and early adulthood bone changes are particularly common in the skull, pelvis, and spine. Pseudotumors of extramedullary hematopoiesis may occur in paravertebral sites and in many other organs and tissues .
极力证明
发表于 2025-3-23 16:40:48
S. Trakadas,G. Pouliades,A. Gouliamos,L. Vlahos,J. Pappas,A. Aesopos,C. Papavasiliou
慢跑鞋
发表于 2025-3-23 19:32:33
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DEAF
发表于 2025-3-24 00:41:01
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考得
发表于 2025-3-24 03:36:15
Osseous X-Ray Findings in Thalassemia Minorcarriers of thalassemia. Therefore, this chapter will deal with bone radiology of thalassemia trait or minor, on the basis of personal experience and the data so far reported on this subject in the literature.
Aids209
发表于 2025-3-24 07:18:16
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Focus-Words
发表于 2025-3-24 12:21:55
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赞美者
发表于 2025-3-24 15:56:56
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盖他为秘密
发表于 2025-3-24 19:48:44
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.
predict
发表于 2025-3-24 23:39:35
Thalassemia: Basic Genetics and Molecular Defectses consist of two pairs of polypeptide chains, each of which constitutes an array of 140–145 amino acids, which are assembled in an extremely precise sequence. This primary structure defines various types of chains and is of utmost importance for accurate coiling (secondary structure) and folding (t