Results 91 to 100 of about 69,540 (312)
Clinical characteristics, treatment, and outcomes of hypoadrenocorticism in dogs
Journal of Small Animal Practice, EarlyView.Objectives To determine the long‐term survival of dogs with hypoadrenocorticism during the period that desoxycorticosterone pivalate has become widely used. Secondary goals were to compare age at diagnosis, median survival times, and age at death for dogs with hyponatraemic and/or hyperkalaemic hypoadrenocorticism and eunatraemic eukalaemic ...
T. N. Sherrod, E. Lashnits, K. F. Lunn
wiley +1 more source
The Novel Use of Stereotactic Radiotherapy for Remnant Adrenal Tissue in Nelson Syndrome
AACE Clinical Case Reports, 2020 : Objective: Recurrent Cushing disease (CD) is a rare complication that occurs in patients who have undergone bilateral adrenalectomy (BLA). We report a case of recurrent CD in a patient with Nelson syndrome and adrenalectomy due to remnant adrenal ...
Alexandra N. Martirossian, MD +4 more
doaj
BMC Endocrine Disorders, 2017 BackgroundThe hypertension cure rate of unilateral adrenalectomy in primary aldosteronism (PA) patients varies widely in existing studies.MethodsWe conducted an observational meta-analysis to summarize the pooled hypertension cure rate of unilateral ...
Yu Zhou, Meilian Zhang, Su Ke, Libin Liu
semanticscholar +1 more source
Wilms Tumor in Children With AMER1/WTX Germline Pathogenic Variants: A Multicenter Case Series
Pediatric Blood &Cancer, Volume 72, Issue 8, August 2025.ABSTRACT Background 10–15% of children with Wilms tumor (WT) have predisposing genetic syndromes. Somatic mutations are frequently identified; however, germline pathogenic variants in AMER1 are much less prevalent and are associated with osteopathia striata with cranial sclerosis (OSCS).
Insiyah Campwala +9 more
wiley +1 more source
Journal of Pharmacological Sciences, 2009 .: The organotin trimethyltin (TMT) is known to cause neuronal degeneration in the murine brain. Earlier studies indicate that TMT-induced neuronal degeneration is enhanced by adrenalectomy.
Makoto Shuto +7 more
doaj
Genetic Testing Referral Rates for Pheochromocytoma and Paraganglioma in an Academic Tertiary Centre
Clinical Endocrinology, Volume 103, Issue 2, Page 147-156, August 2025.ABSTRACT Background Clinical guidelines recommend genetic counselling for all patients with pheochromocytoma or paraganglioma (PPGL). Barriers to accessing genetics evaluation are incompletely understood. The objective of this study was to identify individual‐ and provider‐level barriers to genetic testing.
Brian Ruhle +8 more
wiley +1 more source
Cytological Assessment of Adrenal Tumours: Insights From 22‐Years Single Centre Experience
Clinical Endocrinology, Volume 103, Issue 2, Page 157-166, August 2025.ABSTRACT Objective The incidence of adrenal tumours has increased in the last decades, mainly due to increased use of imaging. The diagnostic evaluation of adrenal masses can be complex and, in some cases, necessitates cytological evaluation. However, concerns remain regarding the potential complications associated with adrenal gland biopsy.
Ana Carasel +3 more
wiley +1 more source
Changes in adenosine 5'-monophosphate-activated protein kinase as a mechanism of visceral obesity in Cushing's syndrome [PDF]
, 2008 OBJECTIVE: Features of the metabolic syndrome such as central obesity with insulin resistance and dyslipidemia are typical signs of Cushing's syndrome and common side effects of prolonged glucocorticoid treatment.
Blerina Kola +31 more
core +1 more source
Bilateral adrenalectomy in the 21st century: when to use it for hypercortisolism?
Endocrine-Related Cancer, 2016 Therapeutic options available for the treatment of Cushing's syndrome (CS) have expanded over the last 5 years. For instance, the efficient management of severe hypercortisolism using a combination of fast-acting steroidogenesis inhibitors has been ...
Carole Guerin +6 more
semanticscholar +1 more source