Results 171 to 180 of about 9,797 (224)
Rapid Adrenal Atrophy Following Excision of an Ectopic Adrenocorticotropin-Secreting Lung Carcinoid Tumor. [PDF]
Mohamed E +4 more
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Severe Cushing Syndrome From Ectopic Adrenocorticotropin Secretion In Metastatic Prostate Cancer Treated With Osilodrostat. [PDF]
Ji B, Lynch LK, Wardlaw SL.
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Large-scale comparison of two immunoassays for adrenocorticotropic hormone in human plasma. [PDF]
Li Y +4 more
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Ultrasound-Guided Jugular Vein Access for Inferior Petrosal Sinus Sampling: A Safe and Feasible Technique. [PDF]
Páez-Granda D +3 more
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Paraneoplastic Cushing Syndrome Unmasking Small Cell Lung Cancer: A Rare Presentation. [PDF]
Malik J, Arshad L.
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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
openaire +2 more sources
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
ACTH precursors characterize the ectopic ACTH syndrome
Clinical Endocrinology, 1994SummaryOBJECTIVE 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. +9 more
openaire +3 more sources
The Lancet, 2001
A 38-year-old male was diagnosed with Cushing's syndrome. Biochemical tests showed hypokalaemia and hypercortisolaemia, with failure of suppression following high dose dexamethasone, suggesting an ectopic or adrenal source. Adrenocorticotrophic hormone levels were >100 IU/L (normal 3–14 IU/L).
DJR Cuthbertson +2 more
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A 38-year-old male was diagnosed with Cushing's syndrome. Biochemical tests showed hypokalaemia and hypercortisolaemia, with failure of suppression following high dose dexamethasone, suggesting an ectopic or adrenal source. Adrenocorticotrophic hormone levels were >100 IU/L (normal 3–14 IU/L).
DJR Cuthbertson +2 more
openaire +1 more source

