Zobrazeno 1 - 10
of 294
pro vyhledávání: '"Joanna Pepke-Zaba"'
Publikováno v:
International Journal of Cardiology Congenital Heart Disease, Vol 17, Iss , Pp 100536- (2024)
Chronic thromboembolic pulmonary disease (CTEPD) with or without pulmonary hypertension (PH) occurs when thromboemboli in pulmonary arteries fail to resolve completely. Pulmonary artery obstructions due to chronic thrombi and secondary microvasculopa
Externí odkaz:
https://doaj.org/article/6231922bd00344ec910c9f65ed66560e
Autor:
Anna Ulrich, Yukyee Wu, Harmen Draisma, John Wharton, Emilia M. Swietlik, Inês Cebola, Eleni Vasilaki, Zhanna Balkhiyarova, Marjo-Riitta Jarvelin, Juha Auvinen, Karl-Heinz Herzig, J. Gerry Coghlan, James Lordan, Colin Church, Luke S. Howard, Joanna Pepke-Zaba, Mark Toshner, Stephen J. Wort, David G. Kiely, Robin Condliffe, Allan Lawrie, Stefan Gräf, Nicholas W. Morrell, Martin R. Wilkins, Inga Prokopenko, Christopher J. Rhodes
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-13 (2024)
Abstract Pulmonary arterial hypertension (PAH) is characterised by pulmonary vascular remodelling causing premature death from right heart failure. Established DNA variants influence PAH risk, but susceptibility from epigenetic changes is unknown. We
Externí odkaz:
https://doaj.org/article/8e50277bf2c448aa930fb3478374f053
Publikováno v:
Advances in Respiratory Medicine, Vol 92, Iss 1, Pp 45-57 (2024)
Chronic thromboembolic pulmonary disease (CTEPD) is a complication of pulmonary embolism (PE). We conducted an online survey of UK PE-treating physicians to understand practices in the follow-up of PE and awareness of CTEPD. The physicians surveyed (
Externí odkaz:
https://doaj.org/article/983e2587edd7415b80f43adc16493724
Autor:
Louise C. Kirkby, Matthew S. Rodgers, Liliana Amaral‐Almeida, Karen Sheares, Mark Toshner, Katherine Bunclark, Aleksandra Bartnik, Dolores Taboada, Choo Ng, Fouad J. Taghavi, Steven Tsui, John E. Cannon, Jonathan R. Weir‐McCall, John G. Coghlan, David P. Jenkins, Joanna Pepke‐Zaba, Stephen P. Hoole
Publikováno v:
Pulmonary Circulation, Vol 13, Iss 3, Pp n/a-n/a (2023)
Abstract Pulmonary endarterectomy (PEA) may not achieve full clearance of vascular obstructions in patients with more distal chronic thromboembolic pulmonary hypertension (CTEPH). Balloon pulmonary angioplasty (BPA) may be indicated to treat these re
Externí odkaz:
https://doaj.org/article/dabd800258ff4bfdb17ac8fc534df12c
Autor:
Hakim Ghani, Joanna Pepke-Zaba
Publikováno v:
Biomedicines, Vol 12, Iss 1, p 46 (2023)
Chronic thromboembolic pulmonary disease results from the incomplete resolution of thrombi, leading to fibrotic obstructions. These vascular obstructions and additional microvasculopathy may lead to chronic thromboembolic pulmonary hypertension (CTEP
Externí odkaz:
https://doaj.org/article/e050eec464144f92b47adc85e0086fb9
Autor:
Sokratis Kariotis, Emmanuel Jammeh, Emilia M. Swietlik, Josephine A. Pickworth, Christopher J. Rhodes, Pablo Otero, John Wharton, James Iremonger, Mark J. Dunning, Divya Pandya, Thomas S. Mascarenhas, Niamh Errington, A. A. Roger Thompson, Casey E. Romanoski, Franz Rischard, Joe G. N. Garcia, Jason X.-J. Yuan, Tae-Hwi Schwantes An, Ankit A. Desai, Gerry Coghlan, Jim Lordan, Paul A. Corris, Luke S. Howard, Robin Condliffe, David G. Kiely, Colin Church, Joanna Pepke-Zaba, Mark Toshner, Stephen Wort, Stefan Gräf, Nicholas W. Morrell, Martin R. Wilkins, Allan Lawrie, Dennis Wang, UK National PAH Cohort Study Consortium
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
Idiopathic pulmonary arterial hypertension is a rare and fatal disease with a heterogeneous treatment response. Here the authors show that unsupervised machine learning of whole blood transcriptomes from 359 patients with idiopathic pulmonary arteria
Externí odkaz:
https://doaj.org/article/f8e37550b75b47d2a53cbd19d4302aa9
Autor:
Matthew S. Rodgers, Louise C. Kirkby, Liliana Amaral‐Almeida, Karen Sheares, Mark Toshner, Dolores Taboada, Choo Ng, John E. Cannon, Luigia D'Errico, Alessandro Ruggiero, Nicholas Screaton, David Jenkins, John G. Coghlan, Joanna Pepke‐Zaba, Stephen P. Hoole
Publikováno v:
Pulmonary Circulation, Vol 12, Iss 4, Pp n/a-n/a (2022)
Abstract Acute lung injury (ALI) is a common but poorly defined and understood complication of balloon pulmonary angioplasty (BPA) for chronic thromboembolic pulmonary hypertension (CTEPH). Little data are available on the medium term clinical outcom
Externí odkaz:
https://doaj.org/article/d5207a7ce6db4003b590a656726e1ecf
Autor:
Raphael W. Majeed, Martin R. Wilkins, Luke Howard, Paul M. Hassoun, Anastasia Anthi, Hector R. Cajigas, John Cannon, Stephen Y. Chan, Victoria Damonte, Jean Elwing, Kai Förster, Robert Frantz, Stefano Ghio, Imad Al Ghouleh, Anne Hilgendorff, Arun Jose, Ernesto Juaneda, David G. Kiely, Allan Lawrie, Stylianos E. Orfanos, Antonella Pepe, Joanna Pepke‐Zaba, Yuriy Sirenko, Andrew J. Swett, Olena Torbas, Roham T. Zamanian, Kurt Marquardt, Achim Michel‐Backofen, Tobiah Antoine, Jochen Wilhelm, Stephanie Barwick, Phillipp Krieb, Meike Fuenderich, Patrick Fischer, Henning Gall, Hossein‐Ardeschir Ghofrani, Friedrich Grimminger, Khodr Tello, Manuel J. Richter, Werner Seeger
Publikováno v:
Pulmonary Circulation, Vol 12, Iss 3, Pp n/a-n/a (2022)
Abstract The Pulmonary Vascular Research Institute GoDeep meta‐registry is a collaboration of pulmonary hypertension (PH) reference centers across the globe. Merging worldwide PH data in a central meta‐registry to allow advanced analysis of the h
Externí odkaz:
https://doaj.org/article/bf4c158677834cef86926affab97c786
Autor:
Laurent Godinas, Keerthana Iyer, Gergely Meszaros, Rozenn Quarck, Pilar Escribano-Subias, Anton Vonk Noordegraaf, Pavel Jansa, Michele D’Alto, Milan Luknar, Senka Milutinov Ilic, Catharina Belge, Olivier Sitbon, Abílio Reis, Stephan Rosenkranz, Joanna Pepke-Zaba, Marc Humbert, Marion Delcroix
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background During the COVID-19 pandemic, most of the health care systems suspended their non-urgent activities. This included the cancellation of consultations for patients with rare diseases, such as severe pulmonary hypertension (PH), resu
Externí odkaz:
https://doaj.org/article/e7151f016f564639a30ce8eab06920d0
Autor:
Sokratis Kariotis, Emmanuel Jammeh, Emilia M. Swietlik, Josephine A. Pickworth, Christopher J. Rhodes, Pablo Otero, John Wharton, James Iremonger, Mark J. Dunning, Divya Pandya, Thomas S. Mascarenhas, Niamh Errington, A. A. Roger Thompson, Casey E. Romanoski, Franz Rischard, Joe G. N. Garcia, Jason X.-J. Yuan, Tae-Hwi Schwantes An, Ankit A. Desai, Gerry Coghlan, Jim Lordan, Paul A. Corris, Luke S. Howard, Robin Condliffe, David G. Kiely, Colin Church, Joanna Pepke-Zaba, Mark Toshner, Stephen Wort, Stefan Gräf, Nicholas W. Morrell, Martin R. Wilkins, Allan Lawrie, Dennis Wang, UK National PAH Cohort Study Consortium
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/cc1c89b6164a4d8d9937f26685d4f667