Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Lisa, Parfitt"'
Autor:
Brett Heasman, Lisa Parfitt
Publikováno v:
Journal for the Theory of Social Behaviour.
Publikováno v:
Journal of Congenital Cardiology, Vol 1, Iss 1, Pp 1-9 (2017)
Congenital heart disease (CHD) is one of the most common causes of pulmonary arterial hypertension (PAH), with a prevalence nearing that of idiopathic PAH in registries. Despite similarities in pulmonary vascular pathology, PAH-CHD differs from idiop
Autor:
Michael A. Gatzoulis, Heba Nashat, Laura C. Price, Lisa Parfitt, Konstantinos Dimopoulos, Carl Harries, Stephen J. Wort, Emily Shaw, Aleksander Kempny
Publikováno v:
Pulmonary hypertension.
Autor:
Benjamin E, Garfield, Alexi, Crosby, Dongmin, Shao, Peiran, Yang, Cai, Read, Steven, Sawiak, Stephen, Moore, Lisa, Parfitt, Carl, Harries, Martin, Rice, Richard, Paul, Mark L, Ormiston, Nicholas W, Morrell, Michael I, Polkey, Stephen John, Wort, Paul R, Kemp
Publikováno v:
Thorax. 74(2)
Skeletal muscle dysfunction is a clinically important complication of pulmonary arterial hypertension (PAH). Growth/differentiation factor 15 (GDF-15), a prognostic marker in PAH, has been associated with muscle loss in other conditions. We aimed to
Autor:
Konstantinos Dimopoulos, Aleksander Kempny, Rafael Alonso-Gonzalez, Stephen J. Wort, Gerhard-Paul Diller, Philip Marino, Lisa Parfitt, Carl Harries, Chiehyang Koo, Michael A. Gatzoulis, Lorna Swan, Maria Alvarez-Barredo, Anselm Uebing
Publikováno v:
International Journal of Cardiology. 167:840-847
Objectives To examine long-term efficacy of disease targeting therapies (DTT) in patients with Eisenmenger syndrome. Methods All adult patients with Eisenmenger syndrome treated with DTT at our institution were included. Functional class (FC), oxygen
Autor:
Kostas Dimopoulos, John Wort, Laura C. Price, Michael A. Gatzoulis, Arif Khokhar, Rafa Alonso, Ann Sturdy, Carl Harries, Lisa Parfitt, Sara Tyebally
Publikováno v:
4.3 Pulmonary Circulation and Pulmonary Vascular Diseases.
Introduction: Intravenous (IV) prostacyclin therapy in patients with severe pulmonary arterial hypertension can be associated with life-threatening complications. Patient education and confidence in local healthcare services is critical to ensuring p
Autor:
Carl Harries, Michael A. Gatzoulis, Lisa Parfitt, Tamera J. Corte, Athol U. Wells, S. John Wort
Publikováno v:
Respirology. 15:1226-1232
Background and objective: Limited data suggest a benefit following sildenafil treatment in patients with pulmonary hypertension (PH) and interstitial lung disease (ILD). The role of sildenafil in the management of PH in ILD is not clear. We report ou
Autor:
Lisa Parfitt, Carl Harries, Laura C. Price, John Wort, Kostantinos Dimopoulos, Martin Carby, Aleksander Kempny, Raphael Alonso, Athol U. Wells, Anna Reed, Andre R. Simon
Publikováno v:
4.3 Pulmonary Circulation and Pulmonary Vascular Disease.
Aims and objectives: Pulmonary hypertension (PH) is a feature of patients with lung disease undergoing lung transplantation (LTx). Sildenafil use in these patients with 9group 39 PH is not routine, although it appears to benefit some patients. In add
Autor:
Nicholas W. Morrell, Lee Jen, Dongmin Shao, S. John Wort, Alexi Crosby, Yang Pieran, Lisa Parfitt, Paul R. Kemp, Carl Harries, Michael I. Polkey, Benjamin Garfield
Publikováno v:
1.2 Rehabilitation and Chronic Care.
Introduction: Skeletal muscle wasting is emerging as an important complication of PAH. GDF-15, a TGFbeta ligand, has been implicated in the development of muscle wasting and is a marker of prognosis in PAH. It may be a potential target for therapeuti
Autor:
Marina Revilla-Martinez, Aleksander Kempny, Lisa Parfitt, John Wort, Laura C. Price, Rafael Alonso-Gonzalez, Beatriz García-Aranda, Carl Harries, K Dimopoulos
Publikováno v:
4.3 Pulmonary Circulation and Pulmonary Vascular Disease.
Background EMPHASIS10 is a novel, easy to use quality of life questionnaire designed for patients with pulmonary hypertension (PH) 1 . We report our experience in using this score and its relation to markers of disease severity. Methods and Results I