Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Evans R. Fernandez Perez"'
Autor:
Jessica Galant-Swafford, Jason Catanzaro, Rosane Duarte Achcar, Carlyne Cool, Tilman Koelsch, Tami J. Bang, David A. Lynch, Rafeul Alam, Rohit K. Katial, Evans R. Fernández Pérez
Publikováno v:
EClinicalMedicine, Vol 75, Iss , Pp 102749- (2024)
Summary: Granulomatous-lymphocytic interstitial lung disease (GLILD) is a lymphoproliferative and granulomatous pulmonary manifestation of primary immune deficiency diseases, notably common variable immunodeficiency (CVID), and is an important contri
Externí odkaz:
https://doaj.org/article/36d7f43c3a694e39af50381f1a7dce69
Publikováno v:
CHEST Pulmonary, Vol 2, Iss 3, Pp 100039- (2024)
Externí odkaz:
https://doaj.org/article/03d6864fac514fd1837e68d91e654d22
Publikováno v:
BMC Pulmonary Medicine, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background Dyspnea impairs quality of life (QOL) in patients with fibrotic hypersensitivity pneumonitis (FHP). The Living with Pulmonary Fibrosis questionnaire (L-PF) assesses symptoms, their impacts and PF-related QOL in patients with any f
Externí odkaz:
https://doaj.org/article/5014256a048c4f8f8f5d9fbcfc7124a7
Autor:
Evans R. Fernandez-Perez, Swati Phalke, Briana Barkes, Kira Rubtsova, Linda S. Powers, James L. Crooks, Lisa A. Maier, Anatoly V. Rubtsov, Katja Aviszus, Philippa Marrack, John W. Kappler, Nabeel Hamzeh, Brenda Warner
Publikováno v:
American journal of respiratory and critical care medicine. 202(7)
Rationale: A subpopulation of B cells (age-associated B cells [ABCs]) is increased in mice and humans with infections or autoimmune diseases. Because depletion of these cells might be valuable in patients with certain lung diseases, the goal was to f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a2447661380ad4896b73d17d8a84523
https://pubmed.ncbi.nlm.nih.gov/32603192
https://pubmed.ncbi.nlm.nih.gov/32603192
Autor:
Julie Morisset, Kerri A. Johannson, Kirk D. Jones, Paul J. Wolters, Harold R. Collard, Simon L. F. Walsh, Brett Ley, Katerina M. Antoniou, Deborah Assayag, Juergen Behr, Francesco Bonella, Kevin K. Brown, Bridget F. Collins, Yvon Cormier, Tamera J. Corte, Ulrich Costabel, Sonye K. Danoff, Kaïssa de Boer, Evans R. Fernandez Perez, Kevin R. Flaherty, Nicole S. L. Goh, Ian Glaspole, Mark G. Jones, Yasuhiro Kondoh, Michael Kreuter, Yves Lacasse, Lisa H. Lancaster, David J. Lederer, Joyce S. Lee, Toby M. Maher, Fernando J. Martinez, Keith C. Meyer, Joshua J. Mooney, Xavier Muñoz Gall, Paul W. Noble, Imre Noth, Justin M. Oldham, Carlos Alberto de Castro Pereira, Venerino Poletti, Moises Selman, Paolo Spagnolo, Elisabetta Renzoni, Luca Richeldi, Christopher J. Ryerson, Jay H. Ryu, Margaret L. Salisbury, Mary E. Strek, Sara Tomassetti, Dominique Valeyre, Carlo Vancheri, Marlies S. Wijsenbeek, Wim Wuyts
Publikováno v:
American Journal of Respiratory and Critical Care Medicine, 197(8), 1036-1044. American Thoracic Society
Rationale: Current diagnosis of chronic hypersensitivity pneumonitis (cHP) involves considering a combination of clinical, radiological, and pathological information in multidisciplinary team discussions. However, this approach is highly variable wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25e11ae02ccf885415e3251ce502835f
https://pure.eur.nl/en/publications/abb44bc7-7b4e-47af-aa28-528f145c8d90
https://pure.eur.nl/en/publications/abb44bc7-7b4e-47af-aa28-528f145c8d90
Autor:
Kevin K. Brown, Zulma X. Yunt, Jeffrey J. Swigris, Tristan J. Huie, David A. Lynch, Barbara L. Goldstein, Rebecca C. Keith, Amy L. Olson, Joshua J. Solomon, Jonathan H. Chung, Stephen B. Hobbs, William J. Janssen, Evans R. Fernandez-Perez
Publikováno v:
Respiratory Medicine. 126:100-104
Purpose Interstitial lung disease is a common extra-articular manifestation of rheumatoid arthritis (RA-ILD) and is associated with significant morbidity and mortality. However, limited data exist regarding predictors of mortality. We sought to exami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c6d8b8121e3a7f7dd63534e86f40da4
https://doi.org/10.1016/j.rmed.2017.03.027
https://doi.org/10.1016/j.rmed.2017.03.027
Publikováno v:
Respiratory Research, Vol 25, Iss 1, Pp 1-2 (2024)
Externí odkaz:
https://doaj.org/article/596d491a24a24d96b2029a3ba60b8f11
Publikováno v:
ERJ Open Research, Vol 10, Iss 1 (2024)
Hypersensitivity pneumonitis is an immunologically mediated form of lung disease, resulting from inhalational exposure to a large variety of antigens. A subgroup of patients with fibrotic hypersensitivity pneumonitis (FHP) develop symptomatic, functi
Externí odkaz:
https://doaj.org/article/db6e020697584ddbae36b6930d8631be
Autor:
Gregory P. Cosgrove, Tristan J. Huie, Kevin K. Brown, Amy L. Olson, Evans R. Fernandez-Perez, Stephen K. Frankel, David Sprunger, Jeffrey J. Swigris, Joshua J. Solomon, Matthew Strand
Publikováno v:
Chest. 146:775-785
BACKGROUND The usual interstitial pneumonia (UIP) pattern of lung injury may occur in the setting of connective tissue disease (CTD), but it is most commonly found in the absence of a known cause, in the clinical context of idiopathic pulmonary fibro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb322cf6930ac24d436fcc8a6058ee0e
https://doi.org/10.1378/chest.13-2388
https://doi.org/10.1378/chest.13-2388
Publikováno v:
Current Respiratory Care Reports. 2:241-247
Over the past decade, it has been increasingly recognized that patients with idiopathic pulmonary fibrosis (IPF) are at risk of both venous thromboembolic disease (VTE) and coronary artery disease (CAD). When present, these co-morbid conditions negat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2f86ff1b602f6d5a5ccebc46b185014
https://doi.org/10.1007/s13665-013-0067-8
https://doi.org/10.1007/s13665-013-0067-8