Results 241 to 250 of about 35,928 (280)
ABSTRACT Background Clinical outcome studies of 21‐hydroxylase deficiency congenital adrenal hyperplasia (21OHD CAH) may be subject to selection bias due to incomplete case ascertainment. This study aimed to develop a methodology for identifying existing CAH cases and explore its utility to study clinical outcomes. Methods 17‐hydroxyprogesterone assays
Joseph McElvaney +7 more
wiley +1 more source
Abstract Background Metformin and glucagon‐like peptide‐1 receptor agonists (GLP‐1 RAs) may reduce the risk of adiposity‐related cancers in patients with type 2 diabetes (T2D). The potential synergistic effects of these treatments on cancer incidence remain unclear, considering their distinct biological mechanisms and their associated effects on body ...
Alex E. Henney +6 more
wiley +1 more source
Too Dry for Primary Adrenal Insufficiency (PAI): PAI Masked by Volume Depletion. [PDF]
Bathla JS +4 more
europepmc +1 more source
Pembrolizumab-Induced Primary Adrenal Insufficiency: A Rare But Life-Threatening Endocrine irAE
Syeda Sarah Raza +2 more
openalex +1 more source
Regulatory T cells in autoimmune primary adrenal insufficiency. [PDF]
Sjøgren T +4 more
europepmc +1 more source
Dual-release hydrocortisone treatment improves serum and peripheral blood mononuclear cell inflammatory and immune profiles in patients with autoimmune primary adrenal insufficiency. [PDF]
Tomasello L +5 more
europepmc +1 more source

