Results 261 to 270 of about 129,829 (283)
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The Journal of Steroid Biochemistry and Molecular Biology, 1995
Ectopic ACTH syndrome represents a cancer-induced amplification of a property [proopiomelanocortin (POMC) peptides production] normally present in the cells from which the cancer originated but with aberrant posttranslational processing of POMC resulting in a greatly elevated secretion of ACTH precursors.
B L, Wajchenberg +5 more
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Ectopic ACTH syndrome represents a cancer-induced amplification of a property [proopiomelanocortin (POMC) peptides production] normally present in the cells from which the cancer originated but with aberrant posttranslational processing of POMC resulting in a greatly elevated secretion of ACTH precursors.
B L, Wajchenberg +5 more
openaire +2 more sources
Hormone Research in Paediatrics, 1998
Isolated ACTH is a rare cause of secondary adrenocortical insufficiency. The diagnosis is made by the demonstration of low cortisol production with low plasma ACTH, absent adrenal responses to stimulation for pituitary or hypothalamus with intact adrenal response to exogenous ACTH, and normal secretory indices of other pituitary hormones.
D A, de Luis, R, Aller, E, Romero
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Isolated ACTH is a rare cause of secondary adrenocortical insufficiency. The diagnosis is made by the demonstration of low cortisol production with low plasma ACTH, absent adrenal responses to stimulation for pituitary or hypothalamus with intact adrenal response to exogenous ACTH, and normal secretory indices of other pituitary hormones.
D A, de Luis, R, Aller, E, Romero
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The Journal of Pediatrics, 1980
A 9 1/2-year-old girl is presented who had cyclical attacks of abdominal pain, vomiting, emotional disturbance, and marked weight change for two years. Associated findings were facial plethora, hypertension, transient hyperglycemia and glycosuria, elevated plasma ACTH, cortisol, and urinary 17-OHCS excretion, and low plasma osmolality with hyponatremia.
T, Sato +5 more
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A 9 1/2-year-old girl is presented who had cyclical attacks of abdominal pain, vomiting, emotional disturbance, and marked weight change for two years. Associated findings were facial plethora, hypertension, transient hyperglycemia and glycosuria, elevated plasma ACTH, cortisol, and urinary 17-OHCS excretion, and low plasma osmolality with hyponatremia.
T, Sato +5 more
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
2015
ACTH-producing pancreatic neuroendocrine tumors (PanNETs) are rare neoplasms, accounting for a minority of all PanNETs. Nevertheless, they are one of the leading non-pulmonary causes of the so-called ectopic ACTH-dependent Cushing’s syndrome (ECS). The first ECS-associated PanNET was described in 1950 by Del Castillo and coworkers.
Uccella, Silvia +2 more
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ACTH-producing pancreatic neuroendocrine tumors (PanNETs) are rare neoplasms, accounting for a minority of all PanNETs. Nevertheless, they are one of the leading non-pulmonary causes of the so-called ectopic ACTH-dependent Cushing’s syndrome (ECS). The first ECS-associated PanNET was described in 1950 by Del Castillo and coworkers.
Uccella, Silvia +2 more
openaire +1 more source
Nihon rinsho. Japanese journal of clinical medicine, 1972
S, Matsukura +4 more
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S, Matsukura +4 more
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