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Titlebook: Endocrine Neoplasms; Andrew Arnold (Chief, Associate Professor of Medic Book 1997 Springer Science+Business Media Dordrecht 1997 Tumor.can

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發(fā)表于 2025-3-21 17:36:03 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Endocrine Neoplasms
編輯Andrew Arnold (Chief, Associate Professor of Medic
視頻videohttp://file.papertrans.cn/310/309719/309719.mp4
叢書(shū)名稱(chēng)Cancer Treatment and Research
圖書(shū)封面Titlebook: Endocrine Neoplasms;  Andrew Arnold (Chief, Associate Professor of Medic Book 1997 Springer Science+Business Media Dordrecht 1997 Tumor.can
描述Andrew Arnold The past several years have been a time of intense excitement and have brought major advances in the understanding and treatment of endocrine neoplasms. This is therefore an excellent point at which to undertake a broad- based overview of the state of the art in endocrine neoplasia for the Cancer Treatment and Research series. Because of the wide and interdisciplinary readership of this series, our aim for each chapter has been to provide ample background for those not highly familiar with the topic, while emphasizing the most recent advances. Furthermore, the chapters have been written with the clinician in mind, whether she or he is an oncologist, endocrinologist, surgeon, generalist, pathologist, or radiologist. As such, the authors‘ mission has been to focus on clinically relevant issues and to present the scientific basis of current or potential future advances in a manner easily digestible to the nonexpert. Endocrine tumors often cause problems for the patient by virtue of their hormonal activity, which may frequently (but certainly not always) over- shadow the adverse consequences related to their mass per se. In fact, it is important to keep in mind that endoc
出版日期Book 1997
關(guān)鍵詞Tumor; cancer treatment; carcinoma; diagnosis; genetics; hormones; pathogenesis; screening; tumorigenesis
版次1
doihttps://doi.org/10.1007/978-1-4615-6355-6
isbn_softcover978-1-4613-7919-5
isbn_ebook978-1-4615-6355-6Series ISSN 0927-3042 Series E-ISSN 2509-8497
issn_series 0927-3042
copyrightSpringer Science+Business Media Dordrecht 1997
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 22:45:02 | 只看該作者
978-1-4613-7919-5Springer Science+Business Media Dordrecht 1997
板凳
發(fā)表于 2025-3-22 04:20:32 | 只看該作者
地板
發(fā)表于 2025-3-22 06:42:15 | 只看該作者
Dina Pereira,Jo?o Leit?o,Rui Baptista a pituitary adenoma and rarely may result from GH-releasing hormone (GHRH) secretion by an extrapituitary tumor. The disease was first described more than a century ago and was the earliest pituitary disorder to be recognized. The clinical features of acromegaly are caused by elevated GH and insulin-like growth factor-I (IGF-I) levels.
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發(fā)表于 2025-3-22 11:30:28 | 只看該作者
Echo Guided Pericardiocentesis,ry products usually do not cause a recognizable clinical syndrome. Consequently, they are the pituitary adenomas most likely to be clinically nonfunctioning, although occasionally other pituitary adenomas may also be clinically nonfunctioning.
6#
發(fā)表于 2025-3-22 13:49:29 | 只看該作者
Growth hormone- and growth-hormone-releasing hormone-producing tumors, a pituitary adenoma and rarely may result from GH-releasing hormone (GHRH) secretion by an extrapituitary tumor. The disease was first described more than a century ago and was the earliest pituitary disorder to be recognized. The clinical features of acromegaly are caused by elevated GH and insulin-like growth factor-I (IGF-I) levels.
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Cancer Treatment and Researchhttp://image.papertrans.cn/e/image/309719.jpg
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發(fā)表于 2025-3-23 03:29:41 | 只看該作者
Dina Pereira,Jo?o Leit?o,Rui Baptista a pituitary adenoma and rarely may result from GH-releasing hormone (GHRH) secretion by an extrapituitary tumor. The disease was first described more than a century ago and was the earliest pituitary disorder to be recognized. The clinical features of acromegaly are caused by elevated GH and insuli
10#
發(fā)表于 2025-3-23 09:11:49 | 只看該作者
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