Results 231 to 240 of about 106,036 (288)
Ethnic differences in plasma aldosterone concentration and regulatory mechanisms of aldosterone: protocol for a systematic review and meta-analysis. [PDF]
Sharma A +3 more
europepmc +1 more source
Abstract A 5‐year‐old male neutered standard poodle, presented with recurrent gingival margin haemorrhage and associated prolongations in prothrombin time and activated partial thromboplastin time, with repeatable demonstration of clinical (bleeding) and laboratory (prothrombin time, activated partial thromboplastin time) resolution with, and relapse ...
Jenny Reeve, Aiden Pang
wiley +1 more source
Occurrence and Patient Characteristics of Aldosterone Dysregulation in Routine Clinical Care: A Population-Based Study. [PDF]
Ljungberg C +9 more
europepmc +1 more source
Hemodynamic changes in pregnancies with impaired fetal growth: A systematic review and meta‐analysis
Maternal cardiovascular adaptation is altered in pregnancies complicated by impaired fetal growth. From the second trimester onwards, lower cardiac output and increased total peripheral vascular resistance emerge, highlighting the need for early hemodynamic monitoring and potential interventions in at‐risk pregnancies.
Britt M. J. G. Kempener +9 more
wiley +1 more source
Malignant hypertension and pseudohyperaldosteronism associated with rifampicin therapy. [PDF]
Szedleski A +4 more
europepmc +1 more source
A Retrospective Study on the Impact of Primary Aldosteronism in Pregnancy (H.A.P.P.I. Study Group)
ABSTRACT Objective Primary aldosteronism (PA) is a common cause of hypertension in young women. However, there is a paucity of data regarding its impact during pregnancy. The primary objective of this study was to describe the occurrence of hypertensive disorders of pregnancy (HDP) in PA.
Diana Oprea +7 more
wiley +1 more source
Quarterly injectable hormonal contraceptive does not increase the activity of the renin-angiotensin-aldosterone system in women without cardiovascular risk factors. [PDF]
de Oliveira AM +6 more
europepmc +1 more source
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

