Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Peter Dorfmuller"'
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:
Benoit Lechartier, Athénaïs Boucly, Sabina Solinas, Deepa Gopalan, Peter Dorfmüller, Teodora Radonic, Olivier Sitbon, David Montani
Publikováno v:
European Respiratory Review, Vol 33, Iss 171 (2024)
Pulmonary veno-occlusive disease (PVOD), also known as “pulmonary arterial hypertension (PAH) with overt features of venous/capillary involvement”, is a rare cause of PAH characterised by substantial small pulmonary vein and capillary involvement
Externí odkaz:
https://doaj.org/article/26126b5e7c2d47f48fd0ba3420c91a76
Publikováno v:
European Respiratory Review, Vol 32, Iss 170 (2023)
Ever since the second world symposium on pulmonary hypertension (PH) held in Evian, France, in 1998, PH has been classified into five major clinical groups. Group 5 PH includes a variety of distinct conditions with unclear and/or multifactorial under
Externí odkaz:
https://doaj.org/article/08be623335614fa0b383eb9f5e5148a1
Autor:
Tom Verbelen, Laurent Godinas, Peter Dorfmüller, Deepa Gopalan, Robin Condliffe, Marion Delcroix
Publikováno v:
European Respiratory Review, Vol 32, Iss 170 (2023)
Chronic thromboembolic pulmonary hypertension (CTEPH) is a rare and potentially life-threatening complication of acute pulmonary embolism. It is characterised by persistent fibro-thrombotic pulmonary vascular obstructions and elevated pulmonary arter
Externí odkaz:
https://doaj.org/article/49849cf8aa6e4edd8e2bf1c3d650151e
Autor:
Robin Condliffe, Charlotte Durrington, Abdul Hameed, Robert A. Lewis, Rajamiyer Venkateswaran, Deepa Gopalan, Peter Dorfmüller
Publikováno v:
European Respiratory Review, Vol 32, Iss 170 (2023)
Pulmonary hypertension (PH) is defined by the presence of a mean pulmonary arterial pressure >20 mmHg. Current guidelines describe five groups of PH with shared pathophysiological and clinical features. In this paper, the first of a series covering a
Externí odkaz:
https://doaj.org/article/f586a7368df846618fa1032ce20be894
Publikováno v:
European Respiratory Review, Vol 32, Iss 170 (2023)
Externí odkaz:
https://doaj.org/article/efca966edf3846a6aac3bb947a646232
Autor:
Jonas Münks, Athiththan Yogeswaran, Tobiah Kevin Antoine, Leonhard Anton Blumrich, Peter Dorfmüller, Hossein Ardeschir Ghofrani, Birgit Assmus, Ralph Theo Schermuly, Akylbek Sydykov
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 5, p 2827 (2024)
Pulmonary hypertension (PH) associated with left heart disease (PH-LHD) is the most common form of PH. In PH-LHD, changes in the pulmonary vasculature are assumed to be mainly caused by pulmonary venous congestion. However, the underlying mechanisms
Externí odkaz:
https://doaj.org/article/621fb10a5a3b47e5a9f9def86d301ff7
Autor:
Julien Caliez, Marianne Riou, Grégoire Manaud, Morad K. Nakhleh, Marceau Quatredeniers, Catherine Rucker-Martin, Peter Dorfmüller, Florence Lecerf, Maria C. Vinhas, Salam Khatib, Hossam Haick, Sylvia Cohen-Kaminsky, Marc Humbert, David Montani, Frédéric Perros
Publikováno v:
Pulmonary Circulation, Vol 10 (2020)
Trichloroethylene exposure is a major risk factor for pulmonary veno-occlusive disease. We demonstrated that trichloroethylene alters the endothelial barrier integrity, at least in part, through vascular endothelial (VE)-Cadherin internalisation, and
Externí odkaz:
https://doaj.org/article/8bc2fb78089d4348807a024be756516a
Autor:
Jason Weatherald, Peter Dorfmüller, Frédéric Perros, Maria-Rosa Ghigna, Barbara Girerd, Marc Humbert, David Montani
Publikováno v:
European Respiratory Review, Vol 29, Iss 156 (2020)
Pulmonary capillary haemangiomatosis (PCH) is a rare and incompletely understood histopathological finding characterised by abnormal capillary proliferation within the alveolar interstitium, which has long been noted to share many overlapping feature
Externí odkaz:
https://doaj.org/article/991f45984aa0470abb975b95e82b21be
Autor:
Morgane Faure, MD, Emmanuel Gomez, MD, Peter Dorfmüller, MD, PhD, Damien Mandry, MD, PhD, Matthieu Canuet, Romain Kessler, François Chabot, Ari Chaouat, MD, PhD
Publikováno v:
Respiratory Medicine Case Reports, Vol 21, Iss C, Pp 74-77 (2017)
Pulmonary veno-occlusive disease is characterized by remodeling of pulmonary arteries, capillaries and venules. We report a case of diffuse lung emphysema and pulmonary veno-occlusive disease with the characteristic of having no airflow limitation. A
Externí odkaz:
https://doaj.org/article/4165ff9aec344b2a9308adb4d72d2700