Search Results - "TOSHNER, Mark R"
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The pulmonary endothelium in acute respiratory distress syndrome: insights and therapeutic opportunities
Published in Thorax (01-05-2016)“…The pulmonary endothelium is a dynamic, metabolically active layer of squamous endothelial cells ideally placed to mediate key processes involved in lung…”
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Plasma Metabolomics Implicates Modified Transfer RNAs and Altered Bioenergetics in the Outcomes of Pulmonary Arterial Hypertension
Published in Circulation (New York, N.Y.) (31-01-2017)“…Pulmonary arterial hypertension (PAH) is a heterogeneous disorder with high mortality. We conducted a comprehensive study of plasma metabolites using…”
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Long-term use of sildenafil in inoperable chronic thromboembolic pulmonary hypertension
Published in Chest (01-08-2008)“…There are currently no licensed medical therapies for inoperable chronic thromboembolic pulmonary hypertension (CTEPH). In this double-blind,…”
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Decreased time constant of the pulmonary circulation in chronic thromboembolic pulmonary hypertension
Published in American journal of physiology. Heart and circulatory physiology (15-07-2013)“…This study analyzed the relationship between pulmonary vascular resistance (PVR) and pulmonary arterial compliance (Ca) in patients with idiopathic pulmonary…”
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StratosPHere 2: study protocol for a response-adaptive randomised placebo-controlled phase II trial to evaluate hydroxychloroquine and phenylbutyrate in pulmonary arterial hypertension caused by mutations in BMPR2
Published in Current controlled trials in cardiovascular medicine (15-10-2024)“…Pulmonary arterial hypertension is a life-threatening progressive disorder characterised by high blood pressure (hypertension) in the arteries of the lungs…”
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Limitations of resting haemodynamics in chronic thromboembolic disease without pulmonary hypertension
Published in The European respiratory journal (01-01-2019)Get full text
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Impaired Natural Killer Cell Phenotype and Function in Idiopathic and Heritable Pulmonary Arterial Hypertension
Published in Circulation (New York, N.Y.) (28-08-2012)“…Beyond their role as innate immune effectors, natural killer (NK) cells are emerging as important regulators of angiogenesis and vascular remodeling. Pulmonary…”
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Approaches to treat pulmonary arterial hypertension by targeting BMPR2: from cell membrane to nucleus
Published in Cardiovascular research (28-09-2021)“…Abstract Pulmonary arterial hypertension (PAH) is estimated to affect between 10 and 50 people per million worldwide. The lack of cure and devastating nature…”
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Pulmonary arterial size and response to sildenafil in chronic thromboembolic pulmonary hypertension
Published in The Journal of heart and lung transplantation (01-06-2010)“…Background Relative area change (RAC) of the proximal pulmonary artery is a measurement of pulmonary artery distensibility and has been shown to correlate with…”
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Prevalence and clinical significance of conduction disease in patients with idiopathic pulmonary arterial hypertension
Published in The Journal of heart and lung transplantation (01-07-2022)“…Anatomical and physiological changes in the right heart as a direct consequence of the upstream pressure overload characteristic of idiopathic pulmonary…”
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Natural history of chronic thromboembolic pulmonary disease with no or mild pulmonary hypertension
Published in The Journal of heart and lung transplantation (01-09-2023)“…We describe baseline characteristics, disease progression and mortality in chronic thromboembolic pulmonary disease patients as a function of mean pulmonary…”
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The lysosomal inhibitor, chloroquine, increases cell surface BMPR-II levels and restores BMP9 signalling in endothelial cells harbouring BMPR-II mutations
Published in Human molecular genetics (15-09-2013)“…Pulmonary arterial hypertension (PAH) is characterized by dysregulated pulmonary artery endothelial cell (PAEC) proliferation, apoptosis and permeability…”
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Joint patient and clinician priority setting to identify 10 key research questions regarding the long-term sequelae of COVID-19
Published in Thorax (01-07-2022)“…Given the large numbers of people infected and high rates of ongoing morbidity, research is clearly required to address the needs of adult survivors of…”
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EmPHasis-10 health-related quality of life score predicts outcomes in patients with idiopathic and connective tissue disease-associated pulmonary arterial hypertension: results from a UK multicentre study
Published in The European respiratory journal (01-02-2021)“…Health-related quality of life (HRQoL) scores assess symptom burden in pulmonary arterial hypertension (PAH) but data regarding their role in prognostication…”
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Traffic exposures, air pollution and outcomes in pulmonary arterial hypertension: a UK cohort study analysis
Published in The European respiratory journal (01-05-2019)“…While traffic and air pollution exposure is associated with increased mortality in numerous diseases, its association with disease severity and outcomes in…”
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Deprivation and prognosis in patients with pulmonary arterial hypertension: missing the effect of deprivation on a rare disease?
Published in The European respiratory journal (01-08-2020)“…In this journal, P ellino et al. [1] presented a survival analysis to assess how deprivation affects prognosis in patients with pulmonary arterial hypertension…”
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Generation and Culture of Blood Outgrowth Endothelial Cells from Human Peripheral Blood
Published in Journal of visualized experiments (23-12-2015)“…Historically, the limited availability of primary endothelial cells from patients with vascular disorders has hindered the study of the molecular mechanisms…”
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Hepatic Shunting of Eggs and Pulmonary Vascular Remodeling in Bmpr2(+/-) Mice with Schistosomiasis
Published in American journal of respiratory and critical care medicine (01-12-2015)“…Schistosomiasis is a major cause of pulmonary arterial hypertension (PAH). Mutations in the bone morphogenetic protein type-II receptor (BMPR-II) are the…”
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Unexplained iron deficiency in idiopathic and heritable pulmonary arterial hypertension
Published in Thorax (01-04-2011)“…Anaemia is common in left heart failure and is associated with a poorer outcome. Many patients with pulmonary arterial hypertension (PAH) are anaemic or…”
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