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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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Developments in Cardiovascular Medicine2]. As a result, the diagnostic dilemma of separating the small fraction of hypersecretory and/or malignant masses from the majority that are nonhypersecretory adrenal adenomas has become common. Given the fourfold greater autopsy incidence of adrenal adenomas compared with the radiographic incidenc
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https://doi.org/10.1007/978-94-009-8287-1 its existence was predicted from the occurrence of ‘insulin reactions’ in nondiabetic persons [1]; in the case of other islet-cell tumors, their existence (glucagonoma, somatostatinoma, VIPoma, PPoma) followed the development of the ability to measure in the circulation the polypeptides that were s
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Treatment of DME with Steroids,ation with pancreatic-duodenal endocrine and anterior pituitary tumors. Other endocrine lesions, such as adrenocortical proliferation; thymic, bronchial, and gastric carcinoids; as well as thyroid adenomas, colloid goiters, differentiated thyroid carcinoma, and lipomas, are over-represented in MEN-I
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Henri J. Dumont,Stefan Schorreelsgnosis. In many patients, the first clinical expression of the syndrome is hyperparathyroidism (HPT). In others, it may be a combination of manifestations, including a functional endocrine pancreatic syndrome and HPT, or a combination of HPT and a pituitary tumor such as a prolactinoma. Occasionally
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0927-3042 nt 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
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