Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Peter J. Engel"'
Autor:
Rohit Gupta, Steven D. Nathan, Oksana A. Shlobin, Jeffrey I. Stewart, Robert P. Baughman, Franck Rahaghi, Elyse E. Lower, Joyce Zeigler, Peter J. Engel
Publikováno v:
Chest. 161:448-457
Background Riociguat is effective in delaying the time to clinical worsening (TCW) in patients with groups 1 and 4 pulmonary hypertension. Research Question Is riociguat more effective than placebo in prolonging TCW in sarcoidosis-associated pulmonar
Autor:
Eva M. Carmona, Laura C. Price, Marlies S. Wijsenbeek, Athol U. Wells, John Wort, Vasilis Kouranos, Joseph Barney, Elyse E. Lower, Oksana A. Shlobin, Peter J. Engel, Esam H. Alhamad, Steven D. Nathan, Scott D. Barnett, Daniel A. Culver, Robert P. Baughman, Sivagini Ganesh, Mary Beth Scholand, Francis Cordova
Publikováno v:
European Respiratory Journal, 55(5):1901747. European Respiratory Society
IntroductionSarcoidosis-associated pulmonary hypertension (SAPH) is associated with reduced survival in single-centre studies. The international Registry for SAPH (ReSAPH) with long-term follow-up was established to enrich our knowledge of this compl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f17bfac43b8ad4a0f2ed11f48d41f2c4
https://pure.eur.nl/en/publications/9fdc0569-bf4a-472b-a140-3a7289a28d86
https://pure.eur.nl/en/publications/9fdc0569-bf4a-472b-a140-3a7289a28d86
Autor:
Robert P. Baughman, Steven D. Nathan, Joseph Barney, Francis Cordova, Daniel A. Culver, Vasilis Kouranos, Joseph G Cal, Elyse E. Lower, Mary Beth Scholand, JoAnne Baran, Marlies S. Wijsenbeek, Oksana A. Shlobin, Sivagini Ganesh, Surinder S. Birring, Athol U. Wells, Peter J. Engel, Eva M. Carmona, Esam H. Alhamad, Lanier O'Hare
Publikováno v:
Respiratory Medicine, 139, 72-78. W.B. Saunders
Baughman, R P, Shlobin, O A, Wells, A U, Alhamad, E H, Culver, D A, Barney, J, Cordova, F C, Carmona, E M, Scholand, M B, Wijsenbeek, M, Ganesh, S, Birring, S S, Kouranos, V, O'Hare, L, Baran, J M, Cal, J G, Lower, E E, Engel, P J & Nathan, S D 2018, ' Clinical features of sarcoidosis associated pulmonary hypertension : Results of a multi-national registry ', Respiratory Medicine, pp. 72-78 . https://doi.org/10.1016/j.rmed.2018.04.015
Baughman, R P, Shlobin, O A, Wells, A U, Alhamad, E H, Culver, D A, Barney, J, Cordova, F C, Carmona, E M, Scholand, M B, Wijsenbeek, M, Ganesh, S, Birring, S S, Kouranos, V, O'Hare, L, Baran, J M, Cal, J G, Lower, E E, Engel, P J & Nathan, S D 2018, ' Clinical features of sarcoidosis associated pulmonary hypertension : Results of a multi-national registry ', Respiratory Medicine, pp. 72-78 . https://doi.org/10.1016/j.rmed.2018.04.015
Background Pulmonary hypertension (PH) is a significant cause of morbidity and mortality in sarcoidosis. We established a multi-national registry of sarcoidosis associated PH (SAPH) patients. Methods Sarcoidosis patients with PH confirmed by right he
Autor:
V. Kouranos, Jan C. Grutters, Joseph Barney, E.M. Carmona Porquera, Peter J. Engel, Marlies S. Wijsenbeek, S. Ganesh, M. Post, A.U. Wells, Mary Beth Scholand, Rohit Gupta, O.A. Shlobin, Esam H. Alhamad, S.D. Nathan, Robert P. Baughman, Daniel A. Culver, M. Huitema, Elyse E. Lower
Publikováno v:
Publons
Publikováno v:
Clinics in Chest Medicine. 36:703-714
Pulmonary hypertension is a complication of sarcoidosis leading to dyspnea and associated with increased morbidity and mortality. Sarcoidosis-associated pulmonary hypertension (SAPH) can be due to several factors, including vascular involvement by th
Autor:
Robert P. Baughman, Peter J. Engel
Publikováno v:
Advances in Pulmonary Hypertension. 14:138-144
Sarcoidosis-associated pulmonary hypertension (SAPH) has been reported in 10% of all sarcoidosis patients. In the United States, the prevalence is similar to that reported for scleroderma. There are several possible mechanisms for SAPH, including vas
Autor:
Peter J. Engel
Publikováno v:
Pulmonary Hypertension and Interstitial Lung Disease ISBN: 9783319499161
During the past two decades, there has been significant progress in the diagnosis and treatment of pulmonary hypertension. As a result of several World Symposia, the definition and classification of PH has been revised and refined. PH is now consider
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f2479ba5880ed6b43650115a1b72ef4
https://doi.org/10.1007/978-3-319-49918-5_2
https://doi.org/10.1007/978-3-319-49918-5_2
Autor:
Robert P. Baughman, Daniel A. Culver, Peter J. Engel, Maria Padilla, Kevin F. Gibson, Elyse E. Lower, Francis Cordova
Publikováno v:
Chest. 145:810-817
Background Sarcoidosis-associated pulmonary hypertension (SAPH) is a common problem in patients with persistent dyspneic sarcoidosis. The objective of this study was to determine the effect of bosentan therapy on pulmonary arterial hemodynamics in pa
Publikováno v:
Chest. 138:1078-1085
Objective: Pulmonary hypertension (PH) has been associated with increased mortality in patients with advanced pulmonary sarcoidosis. Sarcoidosis-associated PH may be the result of left ventricular dysfunction (LVD) or isolated pulmonary vasculature a
Autor:
Robert P. Baughman, Peter J. Engel
Publikováno v:
Medical Hypotheses. 73:448-452
Significant progress has been made in the medical therapy of pulmonary hypertension in recent years, but long term results are still disappointing. We describe the theoretical underpinnings of a surgical procedure which we suggest might prevent or de