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Titlebook: Endocrinology and Diabetes; A Problem-Oriented A Francisco Bandeira,Hossein Gharib,Manuel Faria Book 2014 Springer Science+Business Media N

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樓主: microbe
21#
發(fā)表于 2025-3-25 07:56:49 | 只看該作者
Endocrine Hypertension,y 15 % of hypertensive individuals have secondary hypertension, including renal and endocrine causes..Endocrine hypertension arises mainly from adrenal diseases, such as pheochromocytoma, primary aldosteronism, hyperdeoxycorticosteronism, and Cushing’s syndrome, but it can also be related to acromeg
22#
發(fā)表于 2025-3-25 12:35:03 | 只看該作者
Hirsutism and Virilization,3) or classic congenital adrenal hyperplasia (CCAH) (White and Speiser, Endocr Rev 21:245–291, 2000; New, Mol Cell Endocrinol 211:75–83, 2003). Hirsutism commonly results from relatively benign functional disorders. Sometimes, however, it is the presentation of a more severe disorder, and it may be
23#
發(fā)表于 2025-3-25 19:16:30 | 只看該作者
24#
發(fā)表于 2025-3-25 23:55:55 | 只看該作者
25#
發(fā)表于 2025-3-26 00:32:52 | 只看該作者
26#
發(fā)表于 2025-3-26 06:49:01 | 只看該作者
Tatjana Reichhart,Claudia Pusche endocrine neoplasia type 1, McCune Albright syndrome, familial acromegaly and Carney’s syndrome. Mutations in the aryl hydrocarbon receptor interacting protein (AIP) gene have recently been associated with a predisposition to familial pituitary adenoma, and in particular acromegaly..Acromegaly res
27#
發(fā)表于 2025-3-26 09:40:49 | 只看該作者
Entwicklungspsychologische Grundlagen,p. Later on, a specific management targeting to the aetiology or the symptoms of CS may follow..This chapter will first describe the aetiology of CS, review certain epidemiological data and clinical features, followed by a suggested diagnostic and therapeutic management paradigm.
28#
發(fā)表于 2025-3-26 16:40:59 | 只看該作者
Known applications of RTM processing,y 15 % of hypertensive individuals have secondary hypertension, including renal and endocrine causes..Endocrine hypertension arises mainly from adrenal diseases, such as pheochromocytoma, primary aldosteronism, hyperdeoxycorticosteronism, and Cushing’s syndrome, but it can also be related to acromeg
29#
發(fā)表于 2025-3-26 18:50:00 | 只看該作者
Michael Bannister,Israel Herszberg3) or classic congenital adrenal hyperplasia (CCAH) (White and Speiser, Endocr Rev 21:245–291, 2000; New, Mol Cell Endocrinol 211:75–83, 2003). Hirsutism commonly results from relatively benign functional disorders. Sometimes, however, it is the presentation of a more severe disorder, and it may be
30#
發(fā)表于 2025-3-26 20:59:40 | 只看該作者
Sarah H. Awad,Brady Wagoner,Vlad Glaveanutor begins secreting brief nocturnal pulses of GnRH from the hypothalamic arcuate nucleus that subsequently stimulate the pituitary to release luteinizing hormone (LH) and follicle-stimulating hormone (FSH) (Palmert and Dunkel, N Engl J Med 366:443–453, 2012). A recently discovered hormone, kisspept
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