Results 31 to 40 of about 40,901 (342)

Chromogranin A: From Laboratory to Clinical Aspects of Patients with Neuroendocrine Tumors [PDF]

open access: yes, 2018
Background. Neuroendocrine tumors (NETs) are characterized by having behavior and prognosis that depend upon tumor histology, primary site, staging, and proliferative index.
Baldelli, Roberto   +8 more
core   +1 more source

Clinical and radiological features of pituitary stalk lesions in children and adolescents [PDF]

open access: yesAnnals of Pediatric Endocrinology & Metabolism, 2014
PurposeThe diagnosis of pituitary stalk lesion has been based on clinical feature, radiologic assessment for its critical location and role. This study aimed to investigate clinical symptoms, endocrine disturbance, magnetic resonance imaging (MRI ...
Sung Chul Yoon   +3 more
doaj   +1 more source

Trophic and neurotrophic factors in human pituitary adenomas (Review) [PDF]

open access: yes, 2017
The pituitary gland is an organ that functionally connects the hypothalamus with the peripheral organs. The pituitary gland is an important regulator of body homeostasis during development, stress, and other processes.
Agostinelli, Enzo   +11 more
core   +1 more source

Features of anesthesiological management for transnasal surgical in pituitary adenomas: literature review

open access: yesUkrainian Neurosurgical Journal, 2017
Tumors of the pituitary gland make up about 10% of all neoplasms of the brain, mainly represented by adenomas. A feature of a larger number of adenomas is the symptoms of hypersecretion of the pituitary hormones, which leads to typical changes
Lesia Y. Pechera   +2 more
doaj   +1 more source

Diagnosis and Treatment of Pituitary Adenomas

open access: yesКреативная хирургия и онкология, 2020
Pituitary adenomas are among the most common primary intracranial tumours. They are predominantly benign and account for 10–15 % of all intracranial neoplasms. These tumours are divided into two subgroups: macroadenomas (> 1 cm) and microadenomas (<
O. A. Beylerli   +3 more
doaj   +1 more source

Pituitary tumor-transforming gene in endocrine and other neoplasms: a review and update [PDF]

open access: bronzeEndocrine Related Cancer, 2008
Pituitary tumor-transforming gene (PTTG) was only recently discovered. Its overexpression occurs in a wide variety of endocrine and non-endocrine tumors, including ones of pituitary, thyroid, ovary, breast, prostate, lung, esophagus, colon, and the central nervous system.
Fateme Salehi   +4 more
openalex   +3 more sources

Succinate dehydrogenase (SDH)-deficient renal carcinoma:a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients [PDF]

open access: yes, 2014
Succinate dehydrogenase (SDH)-deficient renal carcinoma has been accepted as a provisional entity in the 2013 International Society of Urological Pathology Vancouver Classification.
Belinsky   +46 more
core   +3 more sources

ACTH-producing carcinoma of the pituitary with refractory Cushing's Disease and hepatic metastases: a case report and review of the literature

open access: yesWorld Journal of Surgical Oncology, 2009
Background Pituitary carcinomas are rare neuroendocrine tumors affecting the adenohypophysis. The hallmark of these lesions is the demonstration of distant metastatic spread. To date, few well-documented cases have been reported in the literature.
Sippel Rebecca   +2 more
doaj   +1 more source

A rare cause of recurrent spontaneous pneumothorax: Birt-hogg-dube syndrome [PDF]

open access: yes, 2018
Birt-Hogg-Dube (BHD) syndrome is an unusual disorder characterized by the triad of cutaneous lesions, renal tumors and lung cysts. In cases with BHD syndrome, the frequency of recurrent pneumothorax is increased due to presence of multiple lung cysts. It
Demirci, M.   +3 more
core   +1 more source

Pituitary metastases as a rare variant of intracranial metastasis

open access: yesБюллетень сибирской медицины, 2008
Metastatiс spread of neoplasms to the pituitary gland is a relatively common finding in autopsy series of cancer patients. The majority of these patients were asymptomatic.
A. V. Osnitskaya, V. Ye. Olyushin
doaj   +1 more source

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