Results 61 to 70 of about 354,714 (311)
Arthritis Care &Research, EarlyView.Objective A leading cause of death among patients with scleroderma (SSc), interstitial lung disease (ILD) remains challenging to prognosticate. The discovery of biomarkers that accurately determine which patients would benefit from close monitoring and aggressive therapy would be an essential clinical tool.
Cristina M. Padilla +13 more
wiley +1 more source
A Noninvasive Circulating Signature of Combined Right Ventricular Pressure and Volume Overload in Tetralogy of Fallot/Pulmonary Atresia/Major Aortopulmonary Collateral Arteries [PDF]
, 2023 Katie L. Clouthier +6 more
openalex +1 more source
Pulmonary Arterial Hypertension
Journal of the American College of Cardiology, 2008 Significant advances in the treatment of pulmonary arterial hypertension (PAH) have occurred over the last 10 years, starting with the approval of epoprostenol in 1998. Subsequently, multiple additional medications have received approval, including a subcutaneous prostacyclin, an inhaled prostacyclin, and oral medications in 2 separate classes.
Chin, Kelly M., Rubin, Lewis J.
openaire +2 more sources
Arthritis Care &Research, Accepted Article.Aims We investigated whether a diagnosis of rheumatoid arthritis (RA) affects the quality of inpatient acute myocardial infarction (AMI) care and long‐term mortality post‐AMI. Methods We analysed data from 784,091 adults, 6,047 with a diagnosis of RA, from England and Wales hospitalised with AMI between 2005 and 2019 from the MINAP registry, linked ...
Megan Butler +8 more
wiley +1 more source
Annals of Pediatric Cardiology, 2014 Congenital coronary-pulmonary artery fistula is a rare condition and is usually associated with pulmonary atresia. We present a 10-year-old girl with circumflex coronary artery to pulmonary artery (PA) fistula with a giant dilated circumflex coronary ...
P S Seetharama Bhat +3 more
doaj +1 more source
The Journal of Thoracic and Cardiovascular Surgery, 1984 Two hundred nine children with congenital heart defects characterized by excessive pulmonary blood flow underwent pulmonary artery banding at The Hospital for Sick Children from January, 1972, through December, 1982. The indications for banding, rather than complete repair, varied with the type of cardiac defect as well as with the year of presentation
R A, Albus +3 more
openaire +2 more sources
Arthritis Care &Research, Accepted Article.Objective Mycophenolate Mofetil (MMF) use in limited cutaneous systemic sclerosis (lcSSc) is relatively uncommon due to the lower fibrotic burden and the predominance of the vascular complications. In vitro observations and clinical data from transplanted patients suggest a protective effect of MMF on endothelial function.
Enrico De Lorenzis +77 more
wiley +1 more source
Pulmonary artery xanthogranuloma [PDF]
European Heart Journal - Cardiovascular Imaging, 2012 A 36-year-old woman with a 6-month history of exertional fatigue was referred for echocardiography. In physical examination, a low-pitched systolic murmur (Grade III/VI) was heard best in the left upper sternal border. Transthoracic echocardiography revealed dilated right cardiac chambers with severe tricuspid regurgitation.
Ali Reza, Moaref +4 more
openaire +2 more sources
Arthritis Care &Research, Accepted Article.Objective Somatic items used in depression assessments can potentially overlap with symptoms related to physical illness, including systemic sclerosis (SSc). No studies have looked at whether somatic depression items may be influenced by diffuse versus limited SSc disease subtypes, which are associated with varying degrees of symptom presentation.
Sophie Hu +109 more
wiley +1 more source
When a pulmonary embolism is not a pulmonary embolism: a rare case of primary pulmonary leiomyosarcoma [PDF]
Journal of Community Hospital Internal Medicine Perspectives, 2015 Arterial leiomyosarcomas account for up to 21% of vascular leiomyosarcomas, with 56% of arterial leiomyosarcomas occurring in the pulmonary artery. While isolated cases of primary pulmonary artery leiomyosarcoma document survival up to 36 months after ...
Nargiz Muganlinskaya +3 more
doaj +1 more source