Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Rafael L. Perez"'
Publikováno v:
Respiratory Medicine Case Reports, Vol 22, Iss C, Pp 109-112 (2017)
Scleroderma-related interstitial lung disease (SSc-ILD) is a pulmonary fibrosing disorder characterized by systemic inflammation and progressive scarring of the lungs that leads to respiratory failure. Although certain immunosuppressive therapies may
Externí odkaz:
https://doaj.org/article/82e89f58f8524ec4accdf12831d69060
Autor:
Joshua J. Mooney, Daniel A. Culver, Sachin Chaudhary, Murali Ramaswamy, Gregory P. Cosgrove, Alpa G. Desai, Sonye K. Danoff, Amy Case, Stephen Weight, Rodeo Abrencillo, Joseph D. Zibrak, Srihari Veeraraghavan, Barry S. Shea, Nitin Y. Bhatt, Maryl Kreider, Doug Moore, Mary Beth Scholand, Shelley L. Schmidt, Thomas H. Schaumberg, Christopher S. King, Borna Mehrad, Justin M. Oldham, Bridget A. Graney, Adrian Shifren, Christophe He, Nathan Sandbo, Nishant Gupta, Michael Marll, Daniel F. Dilling, Tracy Luckhardt, Mridu Gulati, Tristan J. Huie, Craig S. Glazer, Nevins W. Todd, Peter Lacamera, Hyun Koo Kim, Mohamed Saad, Pauline Bianchi, James R. McCormick, Mark Hamblin, Yolanda N. Mageto, Robert Matthew Kottman, Teng Moua, Anna J. Podolanczuk, Scott Matson, Divya Patel, David Roe, Mary E. Strek, Lisa Lancaster, Krishna Thavarajah, Paul J. Wolters, Joyce S. Lee, Sydney B. Montesi, Rafael L. Perez, Rebecca Bascom, Nabeel Hamzeh, Tessy K. Paul, Anoop M. Nambiar, Prema Menon
Publikováno v:
Chest. 159:1517-1530
Background Management of patients with interstitial lung disease (ILD) requires subspecialized, comprehensive, multidisciplinary care. The Pulmonary Fibrosis Foundation established the Care Center Network (CCN) in 2013 with identified criteria to bec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3abc585286feefe6a3c7e92c4e7fac0
https://doi.org/10.1016/j.chest.2020.09.256
https://doi.org/10.1016/j.chest.2020.09.256
Autor:
Rafael L. Perez, Ross Summer
Publikováno v:
The American Journal of the Medical Sciences
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0e4cfe80e3aed8da68741dc2d3d7f40
http://europepmc.org/articles/PMC7357512
http://europepmc.org/articles/PMC7357512
Publikováno v:
The American Journal of the Medical Sciences
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::174e672623194acedb3c08fe9f2b9528
https://pubmed.ncbi.nlm.nih.gov/32690272
https://pubmed.ncbi.nlm.nih.gov/32690272
Publikováno v:
The American journal of the medical sciences. 360(5)
Interstitial lung diseases comprise a family of progressive pulmonary disorders that are often idiopathic or associated with various systemic diseases and that is characterized by bilateral lung involvement with inflammation and tissue remodeling or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2fe8e4b96f187f50ddd258dfc1e7c73
https://pubmed.ncbi.nlm.nih.gov/32487327
https://pubmed.ncbi.nlm.nih.gov/32487327
Publikováno v:
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports, Vol 22, Iss C, Pp 109-112 (2017)
Respiratory Medicine Case Reports, Vol 22, Iss C, Pp 109-112 (2017)
Scleroderma-related interstitial lung disease (SSc-ILD) is a pulmonary fibrosing disorder characterized by systemic inflammation and progressive scarring of the lungs that leads to respiratory failure. Although certain immunosuppressive therapies may
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00b7011fd0fdbf60223f220dba09f2b2
http://europepmc.org/articles/PMC5524221
http://europepmc.org/articles/PMC5524221
Autor:
Jesse Roman, Rafael L. Perez
Publikováno v:
The American Journal of the Medical Sciences
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e439cb5319e8fd60e5791b12696437f
https://doi.org/10.1016/j.amjms.2020.06.001
https://doi.org/10.1016/j.amjms.2020.06.001
Autor:
Charles F. Moore, Rafael L. Perez
Publikováno v:
Current Respiratory Medicine Reviews. 11:83-89
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e372c3b3acea3c352fec98955e6ef76c
https://doi.org/10.2174/1573398x11666150619181948
https://doi.org/10.2174/1573398x11666150619181948
Autor:
Rafael L. Perez, Jesse Roman
Publikováno v:
BioEssays. 41:1900167
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5d4c25a29b63dc5bf3996ddc61de902
https://doi.org/10.1002/bies.201900167
https://doi.org/10.1002/bies.201900167
Publikováno v:
The American Journal of the Medical Sciences. 341:450-453
Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing lung disorder characterized by progressive dyspnea, exercise intolerance and, ultimately, respiratory failure and death. The incidence of IPF seems to be increasing, whereas its etiology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8aa9b47f55114b311bb063ae5daee432
https://doi.org/10.1097/maj.0b013e31821fbdbc
https://doi.org/10.1097/maj.0b013e31821fbdbc