Browsing Centre for Endocrinology by Title
Now showing items 40-59 of 556
-
Beware of epistaxis: fatal pseudoaneurysm rupture 30 years after treatment of acromegaly.
(BMJ Publishing Group, 2024-04-19)We present a fatal complication of treatment in a patient with early-onset acromegaly, treated with two transsphenoidal operations, radiotherapy, radiosurgery and pegvisomant. He was diagnosed in his 30s, and controlled ... -
Bone mineral density, turnover, and microarchitecture assessed by second-generation high-resolution peripheral quantitative computed tomography in patients with Sheehan's syndrome.
(2024-03-20)UNLABELLED: Sheehan's syndrome (SS) is a rare but well-characterized cause of hypopituitarism. Data on skeletal health is limited and on microarchitecture is lacking in SS patients. PURPOSE: We aimed to explore skeletal ... -
Can subunit-specific phenotypes guide surveillance imaging decisions in asymptomatic SDH mutation carriers?
(John Wiley & Sons Ltd, 2019-11-28)Objective With the discovery that familial phaeochromocytoma and paraganglioma syndrome can be caused by mutations in each subunit of the succinate dehydrogenase enzyme (SDH), has come the recognition that mutations in ... -
Cantú syndrome with coexisting familial pituitary adenoma.
(2018-03)CONTEXT: Pseudoacromegaly describes conditions with an acromegaly related physical appearance without abnormalities in the growth hormone (GH) axis. Acromegaloid facies, together with hypertrichosis, are typical manifestations ...