Results 11 to 20 of about 8,113 (209)

Wound, pressure ulcer, and burn guidelines (2023)-4: Guidelines for the management of connective tissue disease/vasculitis-associated skin ulcers, third edition. [PDF]

open access: yesJ Dermatol
The Journal of Dermatology, Volume 52, Issue 6, Page e430-e480, June 2025.
Asano Y   +27 more
europepmc   +2 more sources

Portopulmonary hypertension practice patterns after liver transplantation

open access: yesLiver Transplantation, EarlyView., 2022
Abstract Portopulmonary hypertension (POPH) is a type of pulmonary arterial hypertension occurring exclusively in those with portal hypertensive liver disease. Liver transplantation (LT) can significantly improve outcomes. Current guidelines counsel against immediate adjustments to targeted therapy after LT and suggest routine echocardiography as ...
Arun Jose   +3 more
wiley   +1 more source

CAQ Corner: Basic concepts of transplant immunology

open access: yes, 2022
Liver Transplantation, EarlyView.
Amanda Cheung, Josh Levitsky
wiley   +1 more source

Co-inhibition of Angiotensin II Receptor and Endothelin-1 Attenuates Renal Injury in Unilateral Ureteral Obstructed Mice

open access: yesKidney & Blood Pressure Research, 2016
Background/Aims: Both endothelin-1 (ET-1) and the renin-angiotensin system (RAS) may play important roles in renal fibrosis in the obstructed kidney.
Yoon-Kyung Chang   +5 more
doaj   +1 more source

Distinct ETA receptor binding mode of macitentan as determined by site directed mutagenesis. [PDF]

open access: yesPLoS ONE, 2014
The competitive endothelin receptor antagonists (ERA) bosentan and ambrisentan, which have long been approved for the treatment of pulmonary arterial hypertension, are characterized by very short (1 min) occupancy half-lives at the ET(A) receptor.
John Gatfield   +4 more
doaj   +1 more source

Effect of bosentan therapy in persistent pulmonary hypertension of the newborn

open access: yesPediatrics and Neonatology, 2018
Background: Persistent pulmonary hypertension of the newborn (PPHN) contributes to neonatal hypoxemia and is associated with a high mortality. Some PPHN patients are unresponsive to inhaled nitric oxide (iNO).
Gunlawadee Maneenil   +3 more
doaj   +1 more source

Efficacy and safety of novel-targeted drugs in the treatment of pulmonary arterial hypertension: a Bayesian network meta-analysis

open access: yesDrug Delivery, 2021
Background: Pulmonary arterial hypertension (PAH) is a severe and fatal clinical syndrome characterized by high blood pressure and vascular remodeling in the pulmonary arterioles, which is also a rapidly progressing disease of the lung vasculature with a
Wenhai Fu   +16 more
doaj   +1 more source

Case Report: Bosentan and Sildenafil Exposure in Human Milk - A Contribution From the ConcePTION Project

open access: yesFrontiers in Pharmacology, 2022
Introduction: Quantitative information on disposition of maternal medicines in human milk remains a major knowledge gap. This case report presents the clinical and pharmacokinetic data of a single mother-infant pair exposed to bosentan and sildenafil for
Nina Nauwelaerts   +19 more
doaj   +1 more source

Bosentan and oral anticoagulants in HIV patients: what we can learn of cases reported so far

open access: yesHematology Reports, 2011
Pulmonary arterial hypertension is an infrequent but nevertheless serious life-threatening severe complication of HIV infection. It can be treated with bosentan and oral anticoagulants.
José Antonio Morales-Molina   +3 more
doaj   +1 more source

Cost Effectiveness of Bosentan for Pulmonary Arterial Hypertension: A Systematic Review

open access: yesCanadian Respiratory Journal, 2018
Objectives. Although many studies have reported on the cost-effectiveness of bosentan for treating pulmonary arterial hypertension (PAH), a systematic review of economic evaluations of bosentan is currently lacking.
Ruxu You   +7 more
doaj   +1 more source

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