Results 71 to 80 of about 12,329 (213)

Clinical Practice Patterns in Bone Health Assessment and Management in Endogenous Cushing's Syndrome

open access: yesClinical Endocrinology, Volume 104, Issue 4, Page 302-311, April 2026.
ABSTRACT Objective Skeletal fragility is a common complication of endogenous Cushing's Syndrome (CS), although specific guidelines for managing bone health are lacking. This study aimed to assess clinicians' current engagement with bone health assessment and management in patients with endogenous CS. Design Retrospective‐cohort design. Patients Seventy‐
Preeshila Behary   +10 more
wiley   +1 more source

Adrenocortical neoplasms in children: Treatment and outcomes

open access: yesJournal of Indian Association of Pediatric Surgeons, 2022
Background: Adrenocortical tumors are rare tumors in children with a paucity of outcome data, especially in a resource-challenged setting. Materials and Methods: A retrospective study was conducted to evaluate the presentation, management, and outcomes ...
Vishesh Jain   +9 more
doaj   +1 more source

Ovarian steroid cell tumor with biallelic adenomatous polyposis coli inactivation in a patient with familial adenomatous polyposis [PDF]

open access: yes, 2012
Familial adenomatous polyposis (FAP) is an autosomal dominant cancer predisposition syndrome that accounts for approximately 0.5–1% of all colorectal cancer cases.
Abraham   +36 more
core   +1 more source

NR3C1 Modulates Wnt Signalling to Influence the Invasiveness and Immune Features of Nonfunctioning Invasive Pituitary Adenomas

open access: yesJournal of Cellular and Molecular Medicine, Volume 30, Issue 7, April 2026.
ABSTRACT Pituitary adenomas (PAs) are common intracranial tumours, and invasiveness in nonfunctioning invasive pituitary adenomas (NIPAs) predicts poor prognosis. The molecular mechanisms driving this phenotype remain unclear. This study explored the role of nuclear receptor subfamily 3 group C member 1 (NR3C1) in NIPA invasiveness and its regulation ...
Xiaoping Wang   +6 more
wiley   +1 more source

Adrenal gland tumours. Different clinical presentations in three dogs: a case report

open access: yesVeterinární Medicína, 2013
Three dogs were evaluated due to the presence of unilateral adrenal gland masses with or without clinical signs. Case 1 showed a unilateral non-functional adrenocortical adenoma, discovered accidentally while Case 2 presented a unilateral cortisol ...
A. Loste   +6 more
doaj   +1 more source

O espectro das síndromes de hipertensão esteróide na infância e adolescência [PDF]

open access: yes, 2001
Arterial hypertension is not a privilege of adults. Besides renal and vascular causes, adrenocortical and correlated diseases must be considered when investigating a hypertensive child or adolescent.
Costa-Santos, Marivânia   +1 more
core   +3 more sources

Pure oestrogen-secreting feminizing adrenocortical adenoma. [PDF]

open access: yesArchives of Disease in Childhood, 1977
A 6-year-old boy presented with gynaecomastia. There was no clinical or biochemical evidence of excessive androgenic or glucorticoid activity, but urinary oestrogen levels were raised. An adrenocortical adenoma, demonstrated by x-ray, was surgically removed. Oestrogen levels fell immediately.
E, Bhettay, F, Bonnici
openaire   +2 more sources

Physiological significance of autocrine orexinergic signaling in extra‐hypothalamic tissues

open access: yesPhysiological Reports, Volume 14, Issue 8, April 2026.
Mechanisms of autocrine orexinergic effects in extra‐hypothalamic tissues. Abstract Orexin‐A and orexin‐B, originally discovered as hypothalamic neuropeptides, have been detected in extra‐hypothalamic tissues together with their receptors (OX1R and OX2R) since the early 2000s.
Jean Claude Hakizimana   +2 more
wiley   +1 more source

Aldosterone-secreting adrenocortical adenoma in children

open access: yesJournal of Indian Association of Pediatric Surgeons, 2007
Aldosterone-secreting adrenocortical adenoma is an unusual cause of secondary hypertension in childhood. We describe an eight year-old female child who presented clinically with weakness of lower limbs, headache and hypertension.
Gupta Vipul, Sharma Shyam
doaj  

Infantile virilisation caused by an androstenedione-producing adrenal adenoma

open access: yesJournal of Pediatric Surgery Case Reports, 2019
A previously well fifteen-month-old female infant presented to a district general hospital in the United Kingdom with a three-month history of virilisation developing facial acne, coarse pubic hair, labia majora hypertrophy, menstruation, and clitoral ...
Oliver McCallion   +4 more
doaj   +1 more source

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