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Challenging the known: unusual case report of acromegaly and subclinical Cushing's disease combination. [PDF]
He X, Li H, Wu T, Xu M, Li M, Deng J.
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Autoimmune adrenalitis and an adrenal tumor: a rare cause of elevated 17-hydroxyprogesterone and secondary amenorrhea. [PDF]
Walfish L, Feldman L, Ajise O, Rivera J.
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Paraneoplastic Endocrine Changes in Gastrointestinal Tumors: A Clinical and Mechanistic Review. [PDF]
Forțofoiu D +8 more
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Small-cell carcinoma of the cervix with acute-onset psychotic symptoms associated with clinically diagnosed ectopic ACTH production: a case report. [PDF]
Ozaki K +13 more
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Androgen loss accelerates brain tumour growth via HPA axis activation. [PDF]
Lee J +30 more
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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
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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
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
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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, 1980A 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
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ACTH-Secreting Pheochromocytoma with False-Negative ACTH Immunohistochemistry
Endocrine Pathology, 2012Since 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
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