Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Pia Trip"'
Autor:
Marielle C. van de Veerdonk, Lize Roosma, Pia Trip, Deepa Gopalan, Anton Vonk Noordegraaf, Peter Dorfmüller, Esther J. Nossent
Publikováno v:
European Respiratory Review, Vol 33, Iss 171 (2024)
Pulmonary hypertension (PH) is highly prevalent in patients with left heart disease (LHD) and negatively impacts prognosis. The most common causes of PH associated with LHD (PH-LHD) are left heart failure and valvular heart disease. In LHD, passive b
Externí odkaz:
https://doaj.org/article/b7c58598f6664e63b343dc3efdd2976f
Autor:
Bart Boerrigter, Pia Trip, Harm Jan Bogaard, Herman Groepenhoff, Frank Oosterveer, Nico Westerhof, Anton Vonk Noordegraaf
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e30208 (2012)
INTRODUCTION: It is generally known that positive pressure ventilation is associated with impaired venous return and decreased right ventricular output, in particular in patients with a low right atrial pressure and relative hypovolaemia. Altered lun
Externí odkaz:
https://doaj.org/article/32de4f3f46b54a35ae4be355d7202a08
Autor:
Berend E. Westerhof, Nico Westerhof, Pia Trip, J. A. Groeneveldt, Cathelijne E. E. van der Bruggen, Frances S. de Man, Anton Vonk-Noordergraaf
Publikováno v:
Right ventricle.
Background: Gender is known to play a role in right ventricular (RV) adaption in pulmonary arterial hypertension (PAH). Sex hormone levels change with aging both in males and females. However effect of aging on RV function within sexes has not been e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4930b931398abec9828052695c415a76
https://doi.org/10.1183/13993003.congress-2018.oa1637
https://doi.org/10.1183/13993003.congress-2018.oa1637
Autor:
David Montani, Barbara Girerd, Anco Boonstra, Gilles Garcia, Pia Trip, Herman J Bogaard, Marc Humbert, F.S. de Man, Anton Vonk-Noordegraaf
Publikováno v:
Trip, P, Girerd, B, Bogaard, H J, de Man, F S, Boonstra, A, Garcia, G, Humbert, M, Montani, D & Vonk-Noordegraaf, A 2014, ' Diffusion capacity and BMPR2 mutations in pulmonary arterial hypertension ', European Respiratory Journal, vol. 43, no. 4, pp. 1195-1198 . https://doi.org/10.1183/09031936.00136413
European Respiratory Journal, 43(4), 1195-1198. European Respiratory Society
European Respiratory Journal, 43(4), 1195-1198. European Respiratory Society
To the Editor: Pulmonary arterial hypertension (PAH) is a disease in which remodelling of the small pulmonary arteries leads to an increase in pulmonary artery pressure (PAP). The most important genetic predisposing factor related to PAH is a mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8edd7b6611a199612e29b8d251af4e42
https://doi.org/10.1183/09031936.00136413
https://doi.org/10.1183/09031936.00136413
Autor:
Peter S. Macdonald, Frances S. de Man, C. Tji-Joong Gan, Coen A.C. Ottenheijm, M. Louis Handoko, Pia Trip, Nico Westerhof, Walter Paulus, Carlos Hidalgo, J. Tim Marcus, Chandra Saripalli, Henk Granzier, P E Postmus, Marc Humbert, Cris dos Remedios, Peter Dorfmüller, Jolanda van der Velden, Anton Vonk-Noordegraaf, Silvia Rain, Ger J.M. Stienen, Christophe Guignabert
Publikováno v:
Rain, S, Handoko, M L, Trip, P, Gan, C T, Westerhof, N, Stienen, G J M, Paulus, W J, Ottenheijm, C A C, Marcus, J T, Dorfmuller, P, Guignabert, C, Humbert, M, Macdonald, P, dos Remedios, C, Postmus, P E, Saripalli, C, Hidalgo, C G, Granzier, H L, Vonk-Noordegraaf, A, van der Velden, J & de Man, F S 2013, ' Right ventricular diastolic impairment in patients with pulmonary arterial hypertension ', Circulation, vol. 128, no. 18, pp. 2016-2025 . https://doi.org/10.1161/CIRCULATIONAHA.113.001873
Europe PubMed Central
Circulation, 128(18), 2016-2025. American Heart Association
Circulation, 128(18), 2016-2025. Lippincott Williams and Wilkins
Europe PubMed Central
Circulation, 128(18), 2016-2025. American Heart Association
Circulation, 128(18), 2016-2025. Lippincott Williams and Wilkins
Background— The role of right ventricular (RV) diastolic stiffness in pulmonary arterial hypertension (PAH) is not well established. Therefore, we investigated the presence and possible underlying mechanisms of RV diastolic stiffness in PAH patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3818d424fec346c08c9224db42df8d48
https://doi.org/10.1161/circulationaha.113.001873
https://doi.org/10.1161/circulationaha.113.001873
Autor:
J. Tim Marcus, Harm Jan Bogaard, Cathelijne E. E. van der Bruggen, Anton Vonk Noordegraaf, Esther J. Nossent, Pia Trip, Frances S. de Man, Onno A. Spruijt
Publikováno v:
Pulmonary Circulation
Pulmonary Circulation, 7(1), 137-144. University of Chicago Press
Van Der Bruggen, C E, Spruijt, O A, Nossent, E J, Trip, P, Marcus, J T, De Man, F S, Bogaard, H J & Noordegraaf, A V 2017, ' Treatment response in patients with idiopathic pulmonary arterial hypertension and a severely reduced diffusion capacity ', Pulmonary Circulation, vol. 7, no. 1, pp. 137-144 . https://doi.org/10.1086/690016
Pulmonary Circulation, 7(1), 137-144. University of Chicago Press
Van Der Bruggen, C E, Spruijt, O A, Nossent, E J, Trip, P, Marcus, J T, De Man, F S, Bogaard, H J & Noordegraaf, A V 2017, ' Treatment response in patients with idiopathic pulmonary arterial hypertension and a severely reduced diffusion capacity ', Pulmonary Circulation, vol. 7, no. 1, pp. 137-144 . https://doi.org/10.1086/690016
Patients with idiopathic pulmonary arterial hypertension (IPAH) and a reduced diffusion capacity of the lung for carbon monoxide (DLCO) have a worse survival compared to IPAH patients with a preserved DLCO. Whether this poor survival can be explained
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d81d38958699610072045eb83449b41
https://pubmed.ncbi.nlm.nih.gov/28680573
https://pubmed.ncbi.nlm.nih.gov/28680573
Autor:
Herman Groepenhoff, Anton Vonk-Noordegraaf, Heleen Rietema, Sebastiaan Holverda, Pieter E. Postmus, Pia Trip, Harm Jan Bogaard, Nico Westerhof, Bart Boerrigter, Anco Boonstra
Publikováno v:
Chest. 142:1166-1174
Background Pulmonary hypertension (PH) is a well-recognized complication of COPD. The impact of PH on exercise tolerance is largely unknown. We evaluated and compared the circulatory and ventilatory profiles during exercise in patients with COPD with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82cf91a8a85d8c04e62824ef78024053
https://doi.org/10.1378/chest.11-2798
https://doi.org/10.1378/chest.11-2798
Autor:
Arjan C. Houweling, Cathelijne E. E. van der Bruggen, Harm Jan Bogaard, Marc Humbert, Pia Trip, Anton Vonk Noordegraaf, Frances S. de Man, Nina Rol, Chris Happé, Barbara Girerd, Louis M Handoko, Onno A. Spruijt, Marie-José Goumans, Olaf Mercier, Jolanda van der Velden, Peter Dorfmüller
Publikováno v:
Circulation. 132
Introduction: The effects of a mutation in the bone morphogenetic protein receptor 2 gene (BMPR2) gene on right ventricular (RV)adaptation are currently unknown. Therefore, we investigated RV function in PAH patients with and without BMPR2 mutation b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af5c43bbaad974c93069aeef2cc94746
https://doi.org/10.1161/circ.132.suppl_3.10300
https://doi.org/10.1161/circ.132.suppl_3.10300
Autor:
Frances S. de Man, Pia Trip, Harm Jan Bogaard, Anton Vonk Noordegraaf, Onno A. Spruijt, Cathelijne E. E. van der Bruggen
Publikováno v:
4.3 Pulmonary Circulation and Pulmonary Vascular Disease.
Background: In a subset of patients with idiopathic pulmonary arterial hypertension(IPAH),diffusion capacity for carbon monoxide(DLCO) is severely reduced,which is associated with worse survival and exercise performance.Aim:to compare baseline cardia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b00e9907d3ddbf16a442ffa13e0fc6c8
https://doi.org/10.1183/13993003.congress-2015.pa2465
https://doi.org/10.1183/13993003.congress-2015.pa2465
Autor:
Peter Dorfmüller, Anton Vonk Noordegraaf, Harm Jan Bogaard, M. Louis Handoko, Nina Rol, Barbara Girerd, Marc Humbert, Femke P. M. Hoevenaars, Frances S. de Man, Arjan C. Houweling, J.T. Marcus, Cathelijne E. E. van der Bruggen, Chris Happé, Onno A. Spruijt, Pia Trip, Marie-José Goumans, Olaf Mercier, Jolanda van der Velden
Publikováno v:
Circulation, 133(18), 1747-1760. Lippincott Williams and Wilkins
Circulation
Circulation, 133(18), 1747
van der Bruggen, C E, Happe, C M, Dorfmueller, P, Trip, P, Spruijt, O A, Rol, N, Hoevenaars, F P, Houweling, A C, Girerd, B, Marcus, J T, Mercier, O, Humbert, M, Handoko, M L, van der Velden, J, Noordegraaf, A V, Bogaard, H J, Goumans, M-J & de Man, F S 2016, ' Bone Morphogenetic Protein Receptor Type 2 Mutation in Pulmonary Arterial Hypertension A View on the Right Ventricle ', Circulation, vol. 133, no. 18, pp. 1747-1760 . https://doi.org/10.1161/CIRCULATIONAHA.115.020696
Circulation
Circulation, 133(18), 1747
van der Bruggen, C E, Happe, C M, Dorfmueller, P, Trip, P, Spruijt, O A, Rol, N, Hoevenaars, F P, Houweling, A C, Girerd, B, Marcus, J T, Mercier, O, Humbert, M, Handoko, M L, van der Velden, J, Noordegraaf, A V, Bogaard, H J, Goumans, M-J & de Man, F S 2016, ' Bone Morphogenetic Protein Receptor Type 2 Mutation in Pulmonary Arterial Hypertension A View on the Right Ventricle ', Circulation, vol. 133, no. 18, pp. 1747-1760 . https://doi.org/10.1161/CIRCULATIONAHA.115.020696
Background— The effect of a mutation in the bone morphogenetic protein receptor 2 ( BMPR2 ) gene on right ventricular (RV) pressure overload in patients with pulmonary arterial hypertension is unknown. Therefore, we investigated RV function in pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::980b0bf2ad74a937f2e4d0536ce0e72b
https://pubmed.ncbi.nlm.nih.gov/27572883
https://pubmed.ncbi.nlm.nih.gov/27572883