Results 141 to 150 of about 37,714 (296)
Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience
Emine Çamtosun +4 more
openalex +1 more source
A unique case of adrenal insufficiency coexisting with two primary malignancies
Hilal Bektaş Uysal +4 more
openalex +2 more sources
MON-164 Determinants of Quality of Life in Primary and Secondary Adrenal Insufficiency from Two Large Tertiary Care Centers in the United States [PDF]
Dingfeng Li +6 more
openalex +1 more source
ABSTRACT Objective The effect of transsphenoidal surgery (TSS) on the hypothalamic‐pituitary‐gonadal (HPG) axis in patients with non‐functioning pituitary adenomas (NFPA) is underexplored, especially in women. Our aim was to investigate the HPG axis function before and after TSS, its association with quality of life (QoL), and to identify factors that ...
Victor Hantelius +6 more
wiley +1 more source
Adrenal Insufficiency due to Total Primary Empty Sella Syndrome
Monika Sharma +2 more
openalex +2 more sources
ABSTRACT Objective Growth hormone deficiency (GHD) diagnosis typically requires the performance of two sequential stimulation tests. Glucagon stimulation test (GST) and arginine stimulation test (AST) are widely used. This study aimed to determine the most suitable order of tests.
David Shaki +6 more
wiley +1 more source
Lígia M. Ferreira +5 more
openaire +1 more source
Case report: Primary empty Sella causing secondary adrenal insufficiency and severe yet asymptomatic hyponatremia [PDF]
Siehoon Lah, Almas Wahab, Ammar Wakil
openalex +1 more source
Obesity in Classic Congenital Adrenal Hyperplasia: Mechanisms, Complications and Management
ABSTRACT Classic congenital adrenal hyperplasia (CCAH) is an autosomal recessive genetic disorder primarily caused by 21‐hydroxylase deficiency. Although the survival rate of patients has significantly improved with glucocorticoid replacement therapy, long‐term use of supraphysiological doses and multiple factors inherent to the disease itself have led
Jialin Mu +5 more
wiley +1 more source
ABSTRACT T‐cell/histiocyte‐rich large B‐cell lymphoma (THRLBCL) is a rare subtype of large B‐cell lymphoma (LBCL) for which central nervous system (CNS) relapse remains a devastating complication. The CNS International Prognostic Index (IPI) is usually used to predict the risk of CNS relapse. However, the overall risk of CNS relapse among patients with
Atte Karhu +22 more
wiley +1 more source

