Results 121 to 130 of about 2,227,855 (320)
A Case of Cushing's Syndrome in an Infant [PDF]
, 1958 E. Goldblatt, A H Snaith
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Managing Cushing's disease: the state of the art. [PDF]
, 2014 Cushing's disease is a rare chronic disease caused by a pituitary adenoma, which leads to excess secretion of adrenocorticotropic hormone (ACTH). The over-production of ACTH leads to hyperstimulation of the adrenal glands and a chronic excess of cortisol,
Boscaro M +3 more
core +1 more source
Cushing's Disease in Children: Report of Three Cases
Pediatrics and Neonatology, 2010 Cushing's disease is rare in children and adolescents. We report the clinical presentations of three children with Cushing's disease. All three exhibited the typical symptoms and signs of weight gain and growth retardation.
Ping-Yi Hsu +6 more
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Cushing’s syndrome in pregnancy
Gynecological Endocrinology, 2014 Cushing's syndrome is a rare condition in the general population and is even less common during pregnancy with only a few cases reported in literature. The diagnosis of Cushing's syndrome may be difficult during pregnancy because the typical features of the disorder and pregnancy may overlap.
Nassi, Rossella +3 more
openaire +3 more sources
Equine Veterinary Journal, EarlyView.Abstract Background Clinical signs of pituitary pars intermedia dysfunction (PPID) are frequently mistaken for ‘normal’ ageing and may not be optimally assessed. Objective quality of life (QoL) assessment could improve clinical decision‐making. Objectives To develop an owner‐reported health‐related quality‐of‐life (HRQoL) assessment tool for equines ...
Aline Bouquet +4 more
wiley +1 more source
STUDIES IN CUSHING'S SYNDROME. III. URINARY 17-KETOSTEROIDS IN PATIENTS WITH BILATERAL ADRENAL CORTICAL HYPERPLASIA* [PDF]
, 1959 Joseph W. Jailer +3 more
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Protein kinase A: a quirky prototype
The FEBS Journal, EarlyView.Protein kinase A (PKA) has served as a prototype for establishing kinase fundamentals, including sequence, structure and catalytic mechanism. However, PKA is quirky in some respects. Its regulatory elements are expressed separately, including type I (RI) regulatory subunits that contain unusual disulphide‐linked dimerization and docking domains ...
Matthew G. Gold
wiley +1 more source
Orphanet Journal of Rare Diseases, 2006 The Carney complex (CNC) is a dominantly inherited syndrome characterized by spotty skin pigmentation, endocrine overactivity and myxomas. Skin pigmentation anomalies include lentigines and blue naevi.
Bertherat Jérôme
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Exophthalmos in Cushing's Syndrome [PDF]
, 1958 D. C. Morgan, A. Stuart Mason
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