Results 231 to 240 of about 71,688 (285)

Paraneoplastic Endocrine Changes in Gastrointestinal Tumors: A Clinical and Mechanistic Review. [PDF]

open access: yesInt J Mol Sci
Forțofoiu D   +8 more
europepmc   +1 more source

Small-cell carcinoma of the cervix with acute-onset psychotic symptoms associated with clinically diagnosed ectopic ACTH production: a case report. [PDF]

open access: yesFront Oncol
Ozaki K   +13 more
europepmc   +1 more source

Androgen loss accelerates brain tumour growth via HPA axis activation. [PDF]

open access: yesNature
Lee J   +30 more
europepmc   +1 more source
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The ACTH receptor

Baillière's Clinical Endocrinology and Metabolism, 1996
The ACTH-R is a receptor that has a prominent role in mammalian physiology, but which has been notoriously difficulty to study. The cloning of the gene encoding this receptor in 1992 should permit significant advances in the understanding of the physiology, pharmacology and pathophysiology of ACTH.
A J, Clark, F M, Cammas
openaire   +2 more sources

Dependence on ACTH

Annals of Internal Medicine, 1972
Excerpt To the editor: After reading the recent article by Dr. Kimball (1), we had an opportunity to observe a 40-year-old physician who had been dependent on adrenocorticotrophin (ACTH) for 3 year...
U, Ehrig, J G, Rankin
openaire   +2 more sources

Isolated ACTH deficiency confirmed by ACTH radioimmunoassay

Journal of Endocrinological Investigation, 1980
A 28 year old woman presented with symptoms and biochemical findings suggesting hypoglycemia. Detailed endocrine investigations indicated secondary adrenocortical insufficiency with no rise in plasma ACTH or plasma cortisol following insulin-induced hypoglycemia or vasopressin infusion.
T C, Ooi   +3 more
openaire   +2 more sources

ACTH-Secreting Pheochromocytoma with False-Negative ACTH Immunohistochemistry

Endocrine Pathology, 2012
Since 1955, when Roux published the first association between pheochromocytoma and Cushing’s syndrome, we have come to appreciate the unique features of this unusual clinical entity. Pheochromocytoma represents a rare cause of hypercortisolism, accounting for less than 5 % of ectopic Cushing’s syndrome while less than 1 % of pheochromocytomas is ...
M. F. Cassarino   +6 more
openaire   +5 more sources

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