绕着哥哥问
发表于 2025-3-23 11:29:55
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Limousine
发表于 2025-3-23 16:08:55
Integrable Hierarchies and Modern Physical Theories978-94-010-0720-7Series ISSN 1568-2609
Intend
发表于 2025-3-23 19:51:52
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Keshan-disease
发表于 2025-3-23 23:14:41
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PET-scan
发表于 2025-3-24 06:04:53
A. Marshakovderlying genetic disorders, especially multiple endocrine neoplasia type I and von Hippel-Lindau syndrome, are at an increased risk for developing PNETs. Surgical resection is the primary treatment for functional PNETs. However, the decision for surgery depends on multiple factors, including patient
nonradioactive
发表于 2025-3-24 06:40:23
J. D. Edelstein,M. Gómez-Reinoderlying genetic disorders, especially multiple endocrine neoplasia type I and von Hippel-Lindau syndrome, are at an increased risk for developing PNETs. Surgical resection is the primary treatment for functional PNETs. However, the decision for surgery depends on multiple factors, including patient
古董
发表于 2025-3-24 10:56:01
A. Gorsky,A. Mironova benign monomorphic pituitary corticotroph adenoma that secretes excessive adrenocorticotropic hormone (ACTH). Increased ACTH stimulates secretion of cortisol by the adrenal glands, resulting in supraphysiological levels of endogenous steroid resulting in the combination of symptomatology and findi
radiograph
发表于 2025-3-24 16:02:58
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Confirm
发表于 2025-3-24 21:34:19
V. A. Fateeveral endogenous conditions that result in cortisol excess. Endogenous etiologies are uncommon, but clinicians must recognize the constellation of signs and symptoms to prevent significant morbidity and mortality from the diseases. Clinical suspicion of endogenous hypercortisolism leads to screening
我邪恶
发表于 2025-3-25 00:22:38
Y. Nutkuof intracranial mass such as dulled affect, lethargy, hemiparesis, seizures or failing vision . Their goal of therapy is total removal of the intracranial mass which has arisen from the sellar region and restoration of brain function. Ophthalmologists refer patients with specific visual disturban