Results 251 to 260 of about 129,829 (283)

[⁶⁸Ga]Ga-DOTATATE PET/CT and PET/MR enhances the detection of pituitary ACTH-secreting adenomas in cushing's disease. [PDF]

Front Endocrinol (Lausanne)
Zhang Z, Xu S, Li X, Liu Y, Liu C, Zhou J, Zhang Y.   +6 more
europepmc   +1 more source

Ectopic Cushing Syndrome Due to a Large Mediastinal Neuroendocrine Tumor. [PDF]

JCEM Case Rep
Ramírez-García JA, Garza-García G, Mehta R, Reza-Albarrán AA, De La Peña-López R, Iñiguez-Ariza NM.   +5 more
europepmc   +1 more source

A rare case report of familial glucocorticoid deficiency type 4 (GCCD4) with dilated cardiomyopathy: a 3-year follow-up study. [PDF]

Transl Pediatr
Xun Z, Du Y, Zhao T, Wang Z.
europepmc   +1 more source

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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, I M, Holdaway, R A, Donald, H K, Ibbertson   +3 more
openaire   +2 more sources

ACTH precursors characterize the ectopic ACTH syndrome

Clinical Endocrinology, 1994
SummaryOBJECTIVE ACTH is secreted by the pituitary following processing of larger molecular weight precursors, proopiomelanocortin and pro‐ACTH. Ectopic ACTH syndrome refers to the secretion of ACTH by non‐pituitary tumours, but the predominant circulating form of proopiomelano‐cortin‐related peptides remains unclear.PATIENTS Fifteen patients with ...
Stewart, P. M., Gibson, S., Crosby, S. R., Penn, R., Holder, R., Ferry, D., Thatcher, N., Phillips, P., London, D. R., White, A.   +9 more
openaire   +3 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, A.G. Ambrogio, L. Pagliardini, M. De Martin, V. Barresi, F. Cavagnini, F. Pecori Giraldi   +6 more
openaire   +5 more sources

Acth Dependent Hypertension

Clinical and Experimental Hypertension. Part A: Theory and Practice, 1984
(1984). Acth Dependent Hypertension. Clinical and Experimental Hypertension. Part A: Theory and Practice: Vol. 6, No. 3, pp. 599-646.
B A, Scoggins, D A, Denton, J A, Whitworth, J P, Coghlan   +3 more
openaire   +2 more sources

Isolated ACTH deficiency

Clinical Endocrinology, 1991
Summary. Isolated ACTH deficiency is a rare disorder. We report four cases of this disease which presented to the Department of Endocrinology at Leeds General Infirmary over a one‐year period. The diagnostic clinical and biochemical features of each case are discussed and the pertinent literature is reviewed.
S M, Orme, P E, Belchetz
openaire   +2 more sources

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