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pro vyhledávání: ''
Autor:
Marilyn K. Glassberg, Neil A. Ettinger, Hunter Gillies, Jeffrey J. Swigris, Ganesh Raghu, Roger A. Alvarez, Lisa Lancaster, Kevin R. Flaherty, Steven D. Nathan, Peter Fernandes, James E. Loyd, Parag Shah
Publikováno v:
Chest. 156:A2273-A2275
Autor:
Lisa Lancaster, Peter Fernandes, Parag Shah, Ganesh Raghu, Hunter Gillies, Bo Kim, J.E. Loyd, Kevin R. Flaherty, Roger A. Alvarez, Jeffrey J. Swigris, Neil A. Ettinger, Steven D. Nathan, Marilyn K. Glassberg
Publikováno v:
Chest. 158(2)
Background The interstitial lung diseases include a variety of disorders, many of which are characterized by fibrotic changes (fILD). Of the fILDs, Idiopathic pulmonary fibrosis is the most common. Pulmonary hypertension (PH) frequently complicates f
Autor:
Anders Heiervang Tennøe, Cathrine Brunborg, Øyvind Midtvedt, Trond Mogens Aaløkken, Øyvind Molberg, Thor Ueland, Pål Aukrust, May Britt Lund, Anna-Maria Hoffmann-Vold, Torhild Garen, Aurelija Abraityte
Publikováno v:
Chest. 150:299-306
Markers for early identification of progressive interstitial lung disease (ILD) in systemic sclerosis (SSc) are in demand. Chemokine CCL18, which has been linked to pulmonary inflammation, is an interesting candidate, but data have not been consisten
INTRAPULMONARY SHUNTING IN END-STAGE PULMONARY FIBROSIS COMPLICATED BY SEVERE PULMONARY HYPERTENSION
Autor:
Ariss Derhovanessian, Adrian Mayo, Rajeev Saggar, Richard N. Channick, Zafia Anklesaria, Eric H. Yang, Faisal Shaikh, Rajan Saggar
Publikováno v:
Chest. 156:A173-A174
Autor:
Geertje M. de Boer, Leon M. van den Toorn, Peter Th. W. van Hal, Carla E. M. Hollak, Rogier A.S. Hoek, Michael A. den Bakker, Dennis A. Hesselink, Laura van Dussen
Publikováno v:
Chest. 149:e1-e5
Gaucher disease (GD), a lysosomal storage disorder, may result in end-stage lung disease. We report successful bilateral lung transplantation in a 49-year-old woman with GD complicated by severe pulmonary hypertension and fibrotic changes in the lung
Publikováno v:
Chest. 142:200-207
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, and usually fatal disease, based on a multifaceted and incompletely understood pathogenesis. Some of the cellular and molecular mechanisms of vascular remodeling have been experimentally
Autor:
Thomas K. Waddell, Marco Mura, Shaf Keshavjee, Lianne G. Singer, Mingyao Liu, John Granton, Karen McRae, Masaki Anraku, Zhihong Yun, Marc de Perrot
Publikováno v:
Chest. 141:661-673
Background Pulmonary hypertension (PH) associated with pulmonary fibrosis (PF) is a severe condition with poor outcome. It is unknown whether patients with PF with associated PH (APH) represent a distinct phenotype of the disease. We hypothesized tha
Autor:
Matthew D. Jankowich, Sharon Rounds
Publikováno v:
Chest. 141:222-231
There is increasing clinical, radiologic, and pathologic recognition of the coexistence of emphysema and pulmonary fibrosis in the same patient, resulting in a clinical syndrome known as combined pulmonary fibrosis and emphysema (CPFE) that is charac
Autor:
Clifford S. Deutschman, Jonathan B. Orens, Maria Crespo, Jason D. Christie, Adam Fang, Keith M. Wille, Scarlett L. Bellamy, James C. Lee, Scott M. Palmer, Ann Weinacker, David J. Lederer, Steven M. Kawut, Benjamin A. Kohl, Vivek N. Ahya, Vibha N. Lama, Lorraine B. Ware, Ejigayehu Demissie, Sean Studer
Publikováno v:
Chest. 139:782-787
Background Idiopathic pulmonary fibrosis (IPF) is often associated with elevations in pulmonary artery pressures. Although primary pulmonary arterial hypertension (PAH) has been associated with primary graft dysfunction (PGD), the role of secondary P
Autor:
Olivier Sitbon, Marc Humbert, Eric Hachulla, Pierre-Yves Hatron, Gérald Simonneau, Alice Bérezné, Loïc Guillevin, Pierre Clerson, Luc Mouthon, David Launay
Publikováno v:
Chest. 136:1211-1219
Background Pulmonary arterial hypertension (PAH) is a frequent cause of morbidity and mortality in patients with systemic sclerosis (SSc). PAH is generally considered to be a late complication of limited cutaneous SSc. This study identified and inves