Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Evans R Fernández Pérez"'
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:
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
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
Publikováno v:
BMC Pulmonary Medicine, Vol 20, Iss 1, Pp 1-11 (2020)
Abstract Background Idiopathic pulmonary fibrosis (IPF) is a devastating condition characterized by progressive lung function decline and early mortality. While early accurate diagnosis is essential for IPF treatment, data evaluating the impact of ho
Externí odkaz:
https://doaj.org/article/97a52bc00d3448069c246698ba0f35f4
Autor:
Evans R. Fernández Pérez, James L. Crooks, Jeffrey J. Swigris, Joshua J. Solomon, Michael P. Mohning, Tristan J. Huie, Matthew Koslow, David A. Lynch, Steve D. Groshong, Kaitlin Fier
Publikováno v:
ERJ Open Research, Vol 7, Iss 2 (2021)
Hypersensitivity pneumonitis (HP) is an immunologically mediated form of lung disease resulting from inhalational exposure to any of a large variety of antigens. A subgroup of patients with HP develops pulmonary fibrosis (fibrotic HP; FHP), a signifi
Externí odkaz:
https://doaj.org/article/8b2a2e3a430240638b520ad9129b5e1a
Autor:
Michael P. Mohning, Isabelle Amigues, M. Kristen Demoruelle, Evans R. Fernández Pérez, Tristan J. Huie, Rebecca K. Keith, Amy L. Olson, Zulma X. Yunt, Jonathan H. Chung, Stephen Hobbs, Jeffrey J. Swigris, Joshua J. Solomon
Publikováno v:
ERJ Open Research, Vol 7, Iss 1 (2021)
Externí odkaz:
https://doaj.org/article/b90214532cd74f2d8888596605f36e96
Autor:
Pailin Ratanawatkul, Joshua J. Solomon, Darlene Kim, Marjorie P. George, Lia R. Matarrese McGibbon, M. Kristen Demoruelle, Mehrnaz Maleki-Fischbach, Isabelle Amigues, Liudmila Kastsianok, Evans R. Fernández Pérez
Publikováno v:
ERJ Open Research, Vol 6, Iss 2 (2020)
There are limited data nationwide on the burden of systemic sclerosis (SSc)-related mortality. We aimed to determine recent trends in SSc and SSc-related pulmonary arterial hypertension (PAH) mortality overall and across population subgroups. Using d
Externí odkaz:
https://doaj.org/article/66121d9e104f4f5bae7933140e59ba02
Autor:
Daniel-Costin Marinescu, Ganesh Raghu, Martine Remy-Jardin, William D. Travis, Ayodeji Adegunsoye, Mary Beth Beasley, Jonathan H. Chung, Andrew Churg, Vincent Cottin, Ryoko Egashira, Evans R. Fernández Pérez, Yoshikazu Inoue, Kerri A. Johannson, Ella A. Kazerooni, Yet H. Khor, David A. Lynch, Nestor L. Müller, Jeffrey L. Myers, Andrew G. Nicholson, Sujeet Rajan, Ryoko Saito-Koyama, Lauren Troy, Simon L.F. Walsh, Athol U. Wells, Marlies S. Wijsenbeek, Joanne L. Wright, Christopher J. Ryerson
Publikováno v:
Chest. 162(3):614-629
Recent clinical practice guidelines have addressed the diagnosis of idiopathic pulmonary fibrosis (IPF) and fibrotic hypersensitivity pneumonitis (fHP). These disease-specific guidelines were developed independently, without clear direction on how to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::488490ea0509d3d3440723c7f50ca279
https://doi.org/10.1016/j.chest.2022.06.013
https://doi.org/10.1016/j.chest.2022.06.013
Publikováno v:
European Respiratory Review, Vol 27, Iss 150 (2018)
The availability of epidemiological data relating to interstitial lung diseases (ILDs) has increased over recent years, but information on the prevalence and incidence of ILDs of different aetiologies remains limited. Despite global distribution, the
Externí odkaz:
https://doaj.org/article/4914808166a245638ac40bd84aef8e9f