Results 41 to 50 of about 27,650 (185)

Idiopathic Pulmonary Arterial Hypertension Unmasked by Pregnancy

open access: yesAcute Medicine Journal, 2020
A 31-year old woman presented to the acute medical unit 9 days post-partum with shortness of breath and peripheral oedema. Initially suspected to have either a pulmonary embolism or post-partum cardiomyopathy, she proceeded to have imaging including a CT Pulmonary angiogram and echocardiogram, which were suggestive of pulmonary hypertension and severe ...
A, Maxwell, T, Holman, T, Novak
openaire   +3 more sources

Human Herpesvirus 8 and Pulmonary Hypertension

open access: yesEmerging Infectious Diseases, 2005
Human herpesvirus 8 (HHV-8) antibodies were detected in 1 of 33 patients with pulmonary hypertension (including in 1 of 16 with idiopathic pulmonary arterial hypertension), 5 of 29 with cystic fibrosis, and 3 of 13 with interstitial lung disease.
Emanuele Nicastri   +8 more
doaj   +1 more source

Long-Term Survival in Idiopathic Pulmonary Arterial Hypertension Associated with Massive Pulmonary Artery Dilation

open access: yesCanadian Respiratory Journal, 2011
The present report describes two patients with long-term survival after being diagnosed with idiopathic pulmonary arterial hypertension more than 20 years earlier.
Vanja Petrovic   +2 more
doaj   +1 more source

Pulmonary Hypertension Registry: a single-center experience in Egypt

open access: yesEgyptian Journal of Chest Disease and Tuberculosis, 2020
Introduction Pulmonary hypertension is a life-threatening progressive disease that eventually leads to disability and death. Aim To establish the first single-center registry for pulmonary hypertension in Egypt, Kasr Al-Ainy Hospitals, Cairo University ...
Youssef A Soliman   +11 more
doaj   +1 more source

Pulmonary Artery Pulse Wave Velocity in Idiopathic Pulmonary Arterial Hypertension

open access: yesCanadian Journal of Cardiology, 2013
Idiopathic pulmonary artery (PA) hypertension (IPAH) is associated with severe PA remodelling. Although the resulting increase in pulse wave velocity (PWV) might be of major pathophysiological relevance, little is known about PA-PWV in IPAH. The aim of this study was to characterize PA-PWV and its predictors in patients with IPAH.We studied 26 ...
Kopeć, Grzegorz   +5 more
openaire   +3 more sources

Review of the Molecular and Developmental Basis of Myhre Syndrome, Bench Research

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MS) is a connective‐tissue disorder within the acromelic dysplasia spectrum. It is characterized by congenital craniofacial, skeletal, cutaneous anomalies, respiratory, cardiovascular along with intellectual disability, deafness, and progressive fibrosis.
Camille Viaut, Valerie Cormier‐Daire
wiley   +1 more source

Autoimmunity Is a Significant Feature of Idiopathic Pulmonary Arterial Hypertension

open access: yesAmerican Journal of Respiratory and Critical Care Medicine, 2021
Abstract Rationale Autoimmunity is believed to play a role in idiopathic pulmonary arterial hypertension (IPAH). It is not clear whether this is causative or a bystander of disease and if it carries any prognostic or treatment significance.
Jones R. J.   +77 more
openaire   +4 more sources

Cytokine Pathways Driving Diverse Tissue Pathologies in Rheumatoid Arthritis

open access: yesArthritis &Rheumatology, EarlyView.
Rheumatoid arthritis (RA) is a complex systemic disorder characterized primarily by articular inflammation and destruction with associated functional loss and reduced quality of life. RA is also associated with extra‐articular disease, such as that of the lung, with potentially devastating clinical consequences. The critical importance of comorbidities,
Aurelie Najm   +2 more
wiley   +1 more source

A pilot study to examine association of BMI with functional class and 6 min walk distance in idiopathic and heritable PAH: Possible association with estrogen metabolism

open access: yesPulmonary Circulation, 2022
The hypothesis that a relationship exists between body mass index (BMI), functional class, and 6 min walk distance (6MWD) in Group 1‐pulmonary arterial hypertension (PAH) was examined.
Margaret R. MacLean   +7 more
doaj   +1 more source

Pulmonary artery dissection in long standing idiopathic pulmonary arterial hypertension: A case report

open access: yesRadiology Case Reports, 2022
Pulmonary arterial dissection (PAD) is a rare and often lethal complication of chronic pulmonary arterial hypertension (PAH), which may occurs in patients with idiopathic pulmonary arterial hypertension (IPAH) and potentially in those with connective ...
Luis Regalado, BS, MSc   +5 more
doaj   +1 more source

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