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Titlebook: ALERT ? Adverse Late Effects of Cancer Treatment; Volume 2: Normal Tis Philip Rubin,Louis S. Constine,Lawrence B. Marks Book 2014 The Edito

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樓主: 拖累
41#
發(fā)表于 2025-3-28 17:30:22 | 只看該作者
42#
發(fā)表于 2025-3-28 22:04:20 | 只看該作者
Philip Rubin,Louis S. Constine,Lawrence B. MarksComprehensively documents potential late effects in all the normal tissue sites in the human body.Considers in detail the detection, diagnosis, management and prevention of effects and discusses progn
43#
發(fā)表于 2025-3-29 01:31:54 | 只看該作者
Medical Radiologyhttp://image.papertrans.cn/a/image/142920.jpg
44#
發(fā)表于 2025-3-29 03:43:47 | 只看該作者
https://doi.org/10.1007/978-3-540-75863-1Cancer Treatment; Chemotherapy; Late Effects; Radiation; Radiotherapy; Diagnostic Radiology; Radiaton Onco
45#
發(fā)表于 2025-3-29 09:21:13 | 只看該作者
978-3-662-51850-2The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer-Verlag GmbH, DE
46#
發(fā)表于 2025-3-29 13:23:18 | 只看該作者
ALERT ? Adverse Late Effects of Cancer Treatment978-3-540-75863-1Series ISSN 0942-5373 Series E-ISSN 2197-4187
47#
發(fā)表于 2025-3-29 16:43:24 | 只看該作者
Apps effektiv managen und vermarktend by a review of the clinical presentation and management of the late oral adverse events in cancer patients. As the oral tissues involved are variable, the nature and quantity of late oral complications are extremely diverse. The impact of these oral complications can result in significantly debili
48#
發(fā)表于 2025-3-29 22:53:12 | 只看該作者
Apps effektiv managen und vermarktenre highly sensitive to various treatment modalities and their damage following therapy leads frequently to functional abnormalities such as xerostomia, dysphagia, aspiration, hearing loss, and others, reducing substantially the quality of life of survivors. The anatomy of these organs, their toleran
49#
發(fā)表于 2025-3-30 03:03:43 | 只看該作者
50#
發(fā)表于 2025-3-30 06:18:35 | 只看該作者
Multi-domain Models of Internalizing Disorders: Risk Factors and Complex Pathways,ng two different multidomain models for each symptom type. The first models for each symptom type included pathways from risk factors in different domains at age 4 to age 5 risk factors, and then to child symptoms at age 6. The second models, developed to examine risk factors associated with . in de
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