標(biāo)題: Titlebook: Endocrine Neoplasms; Andrew Arnold (Chief, Associate Professor of Medic Book 1997 Springer Science+Business Media Dordrecht 1997 Tumor.can [打印本頁(yè)] 作者: 字里行間 時(shí)間: 2025-3-21 17:36
書(shū)目名稱(chēng)Endocrine Neoplasms影響因子(影響力)
作者: 不來(lái) 時(shí)間: 2025-3-21 22:45
978-1-4613-7919-5Springer Science+Business Media Dordrecht 1997作者: 阻擋 時(shí)間: 2025-3-22 04:20 作者: circuit 時(shí)間: 2025-3-22 06:42
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.作者: deadlock 時(shí)間: 2025-3-22 11:30
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.作者: Enzyme 時(shí)間: 2025-3-22 13:49
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.作者: Enzyme 時(shí)間: 2025-3-22 19:13 作者: Tempor 時(shí)間: 2025-3-22 23:29
Cancer Treatment and Researchhttp://image.papertrans.cn/e/image/309719.jpg作者: spinal-stenosis 時(shí)間: 2025-3-23 03:29
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作者: 獸皮 時(shí)間: 2025-3-23 09:11 作者: 向前變橢圓 時(shí)間: 2025-3-23 12:30 作者: Coma704 時(shí)間: 2025-3-23 15:36 作者: 不可磨滅 時(shí)間: 2025-3-23 20:56
Mass, momentum, and geodynamics,detect asymptomatic masses in several organs [1]. Such incidentally found masses have been referred to as . [2]. When these imaging techniques have been applied to the pituitary gland, similar incidentalomas have been found in seemingly normal subjects [3–11]. At present, these techniques include hi作者: 沉著 時(shí)間: 2025-3-23 22:12
Heritable Variation in Populations,yroid carcinomas. The rest are, in decreasing order of frequency, medullary carcinomas, lymphomas, sarcomas, squamous-cell carcinomas, and metastases from tumors elsewhere. Besides being extremely rare, all of the latter, with the exception of medullary thyroid carcinoma, are tumors derived from non作者: 阻礙 時(shí)間: 2025-3-24 03:41 作者: 山羊 時(shí)間: 2025-3-24 08:20 作者: 辮子帶來(lái)幫助 時(shí)間: 2025-3-24 14:01 作者: 利用 時(shí)間: 2025-3-24 18:03
David A. Edelman,Gary S. Berger,Louis Keithcells in bone [1]. However, in 1936 Gutman et al. documented the occurrence of hypercalcemia and hypophosphatemia in a patient with bronchogenic carcinoma who had no osseous metastases and no obvious parathyroid dysfunction [2]. An interesting conceptual breakthrough was later provided by Fuller Alb作者: 螢火蟲(chóng) 時(shí)間: 2025-3-24 19:00 作者: FIN 時(shí)間: 2025-3-25 00:12 作者: 碎石頭 時(shí)間: 2025-3-25 03:57
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作者: triptans 時(shí)間: 2025-3-25 08:31 作者: 暗指 時(shí)間: 2025-3-25 13:58
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作者: Infelicity 時(shí)間: 2025-3-25 19:02 作者: 你敢命令 時(shí)間: 2025-3-25 23:47
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作者: manifestation 時(shí)間: 2025-3-26 01:08
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作者: 議程 時(shí)間: 2025-3-26 06:15
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作者: artifice 時(shí)間: 2025-3-26 12:27 作者: heartburn 時(shí)間: 2025-3-26 15:18 作者: hereditary 時(shí)間: 2025-3-26 20:08 作者: Anthology 時(shí)間: 2025-3-26 21:42 作者: 不可侵犯 時(shí)間: 2025-3-27 04:29
Book 1997crine 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 p作者: 焦慮 時(shí)間: 2025-3-27 08:59
Follicular cell-derived thyroid carcinomas,from tumors elsewhere. Besides being extremely rare, all of the latter, with the exception of medullary thyroid carcinoma, are tumors derived from nonendocrine tissues, and therefore they are not the subject of this review. Medullary thyroid carcinoma is covered in Chapter 20.作者: 約會(huì) 時(shí)間: 2025-3-27 09:30
Parathyroid carcinoma,sm, and when recurrences eventually occur they are predominantly located cervically. This fact may initially lead the surgeon to assume that the tumor is not malignant. The term . was coined for borderline lesions with a clinically benign course [1].作者: 暴發(fā)戶(hù) 時(shí)間: 2025-3-27 14:10 作者: 解決 時(shí)間: 2025-3-27 21:33 作者: machination 時(shí)間: 2025-3-28 00:08 作者: Fsh238 時(shí)間: 2025-3-28 02:13
David A. Edelman,Gary S. Berger,Louis Keithtulated that the tumor released a parathyroid hormone (PTH)-like factor that could not only stimulate bone resorption but could also induce phosphaturia, leading to hypophosphatemia. The concept of . or . as a cause of hypercalcemia in malignancy (HM) was thus born.作者: choroid 時(shí)間: 2025-3-28 06:28 作者: 洞察力 時(shí)間: 2025-3-28 14:23 作者: slipped-disk 時(shí)間: 2025-3-28 18:08 作者: 叢林 時(shí)間: 2025-3-28 22:16 作者: bisphosphonate 時(shí)間: 2025-3-29 01:47
Viktor Matej?ík,Zora Haviarová,Juraj ?teňohey were exposed to radiation. The U.S. Government belatedly confirmed that many individuals had been exposed to radiation released from the Hanford nuclear reactor and from other nuclear installations.作者: 最高峰 時(shí)間: 2025-3-29 04:22 作者: –FER 時(shí)間: 2025-3-29 08:52
Management of Antepartum Fetal Deathhe cell biology of these tumors has also been done, mostly in the last decade. Rapidly advancing knowledge in the biology of other more frequent nonendocrine or endocrine tumors promises that better understanding of adrenal tumorigenesis is also forthcoming.作者: Nonflammable 時(shí)間: 2025-3-29 12:40
Prolactinomas,ipple stimulation itself elicits progressively less prolactin release, and in the weeks following initiation of lactation both basal and nursing-stimulated prolactin pulses decrease [2]. Within 4–6 months postpartum, basal prolactin levels are normal without a nursing-induced rise, despite continued lactation.作者: champaign 時(shí)間: 2025-3-29 18:08
Approach to the incidentally discovered pituitary mass,ration of gadolinium [12,13]. It is the purpose of the present discussion to provide information and guidelines for the evaluation of the patient incidentally found to have a mass lesion of the pituitary on a CT or MRI scan that has been performed for some other reason (Fig. 1).作者: progestin 時(shí)間: 2025-3-29 23:15 作者: 蛛絲 時(shí)間: 2025-3-30 00:24 作者: 字形刻痕 時(shí)間: 2025-3-30 06:44
Neoplasms of the adrenal cortex Clinical and basic aspects,he cell biology of these tumors has also been done, mostly in the last decade. Rapidly advancing knowledge in the biology of other more frequent nonendocrine or endocrine tumors promises that better understanding of adrenal tumorigenesis is also forthcoming.作者: 整理 時(shí)間: 2025-3-30 09:52
Developments in Cardiovascular Medicinee, and the oncology data that only 20–41% of adrenal metastases are detected by CT [1,3], it is likely that an increase in prevalence will occur if the spatial resolving capacity of abdominal imaging improves, if abdominal imaging occurs more frequently, and if routine abdominal imaging slice thickness is decreased.作者: 山羊 時(shí)間: 2025-3-30 15:56
D. Soga,R. Beer,J. Andrae,B. Bader the budding of isolated endocrine cells and islets from pancreatic duct cells, and severe infantile hypoglycemia [1]. Recent findings have elucidated the molecular cause for hyperinsulinemia in some families with this disorder, providing additional insight into the regulation of insulin secretion.作者: FECK 時(shí)間: 2025-3-30 19:20
Henri J. Dumont,Stefan Schorreels, an MEN-I patient may present with clinical manifestations in all three organs simultaneously. This discussion will be limited to the surgical management of the parathyroid and pancreatic components of the syndrome.作者: 潛伏期 時(shí)間: 2025-3-30 23:53 作者: Cougar 時(shí)間: 2025-3-31 01:44
Persistent hyperinsulinemic hypoglycemia of infancy, the budding of isolated endocrine cells and islets from pancreatic duct cells, and severe infantile hypoglycemia [1]. Recent findings have elucidated the molecular cause for hyperinsulinemia in some families with this disorder, providing additional insight into the regulation of insulin secretion.作者: ventilate 時(shí)間: 2025-3-31 09:00 作者: amphibian 時(shí)間: 2025-3-31 10:15 作者: 柏樹(shù) 時(shí)間: 2025-3-31 17:00 作者: Desert 時(shí)間: 2025-3-31 20:39
Gastrin-producing tumors,e. In this chapter this general usage will be retained. Therefore, a tumor in which gastrin is detected, without associated hypergastrinemia or gastric hypersecretion, would not be included in the general use of this term. Tumors that produce gastrin but are not associated with hypergastrinemia clin作者: 疏遠(yuǎn)天際 時(shí)間: 2025-3-31 21:54
Multiple endocrine neoplasia type I Clinical genetics and diagnosis,cal MEN-I lesions almost invariably are benign but nevertheless may lead to considerable endocrine morbidity [6–10]. Early diagnosis and timely treatment instituted in order to avoid malignancy and endocrine morbidity comprise an increasing concern in MEN-I.作者: Aviary 時(shí)間: 2025-4-1 04:25 作者: WAG 時(shí)間: 2025-4-1 09:46
Treatment of DME with Steroids,cal MEN-I lesions almost invariably are benign but nevertheless may lead to considerable endocrine morbidity [6–10]. Early diagnosis and timely treatment instituted in order to avoid malignancy and endocrine morbidity comprise an increasing concern in MEN-I.作者: 進(jìn)取心 時(shí)間: 2025-4-1 10:56
Somatostatin analogs and receptors Diagnostic and therapeutic applications,作者: 存在主義 時(shí)間: 2025-4-1 14:26
Andrew Arnold (Chief, Associate Professor of Medic
