Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Ipf-Pro Registry investigators"'
Autor:
Joao A. de Andrade, Tejaswini Kulkarni, Megan L. Neely, Anne S. Hellkamp, Amy Hajari Case, Daniel A. Culver, Kalpalatha Guntupalli, Shaun Bender, Craig S. Conoscenti, Laurie D. Snyder, the IPF-PRO Registry Investigators
Publikováno v:
Respiratory Research, Vol 23, Iss 1, Pp 1-9 (2022)
Abstract Background Performance benchmarks for the management of idiopathic pulmonary fibrosis (IPF) have not been established. We used data from the IPF-PRO Registry, an observational registry of patients with IPF managed at sites across the US, to
Externí odkaz:
https://doaj.org/article/d9cb1522f4b141099d73e79e8b59d74e
Autor:
Hyun J. Kim, Laurie D. Snyder, Ayodeji Adegunsoye, Megan L. Neely, Shaun Bender, Eric S. White, Craig S. Conoscenti, Mary E. Strek, The IPF-PRO Registry Investigators
Publikováno v:
Respiratory Research, Vol 22, Iss 1, Pp 1-9 (2021)
Abstract Background Hospitalizations are common among patients with idiopathic pulmonary fibrosis (IPF). We investigated the impact of hospitalizations on outcomes in patients with IPF. Methods The IPF-PRO Registry is an observational US registry tha
Externí odkaz:
https://doaj.org/article/14977bb188b74aeda3d88b1022eb8c36
Autor:
Jamie L. Todd, Richard Vinisko, Yi Liu, Megan L. Neely, Robert Overton, Kevin R. Flaherty, Imre Noth, L. Kristin Newby, Joseph A. Lasky, Mitchell A. Olman, Christian Hesslinger, Thomas B. Leonard, Scott M. Palmer, John A. Belperio, on behalf of the IPF-PRO Registry investigators
Publikováno v:
BMC Pulmonary Medicine, Vol 20, Iss 1, Pp 1-12 (2020)
Abstract Background Matrix metalloproteinases (MMPs) and tissue inhibitors of MMPs (TIMPs) play important roles in the turnover of extracellular matrix and in the pathogenesis of idiopathic pulmonary fibrosis (IPF). This study aimed to determine the
Externí odkaz:
https://doaj.org/article/e7f3bff0a88945d383d884e06a0c2594
Autor:
Jamie L. Todd, Megan L. Neely, Robert Overton, Katey Durham, Mridu Gulati, Howard Huang, Jesse Roman, L. Kristin Newby, Kevin R. Flaherty, Richard Vinisko, Yi Liu, Janine Roy, Ramona Schmid, Benjamin Strobel, Christian Hesslinger, Thomas B. Leonard, Imre Noth, John A. Belperio, Scott M. Palmer, on behalf of the IPF-PRO Registry investigators
Publikováno v:
Respiratory Research, Vol 20, Iss 1, Pp 1-13 (2019)
Abstract Background Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease for which diagnosis and management remain challenging. Defining the circulating proteome in IPF may identify targets for biomarker development. We sought to quantif
Externí odkaz:
https://doaj.org/article/e7e9aa1e37874cbe8ab7871c8f6fedf1
Autor:
Laurie Snyder, Megan L. Neely, Anne S. Hellkamp, Emily O’Brien, Joao de Andrade, Craig S. Conoscenti, Thomas Leonard, Shaun Bender, Mridu Gulati, Daniel A. Culver, Robert J. Kaner, Scott Palmer, Hyun Joo Kim, on behalf of the IPF-PRO™ Registry investigators
Publikováno v:
Respiratory Research, Vol 20, Iss 1, Pp 1-10 (2019)
Abstract Background Idiopathic pulmonary fibrosis (IPF) is a progressive disease with a variable clinical course and high mortality. We used data from a large national US registry of patients with IPF to investigate relationships between patient char
Externí odkaz:
https://doaj.org/article/220745ba1bec4eea82f942d3f9caea4e
Akademický článek
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Akademický článek
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Autor:
J. Oldham, M.L. Neely, H. Mulder, J.A. Belperio, N.M. Patel, C. Hesslinger, J.L. Todd, null on behalf of the IPF-PRO Registry investigators
Publikováno v:
B103. OUTCOMES AND BIOMARKERS IN ILD.
Autor:
M. Neely, S. Bender, A.S. Hellkamp, J.L. Todd, T. Liesching, T.R. Luckhardt, J.M. Oldham, R. Raj, E.S. White, S.M. Palmer, null on behalf of the IPF-PRO Registry investigators
Publikováno v:
B103. OUTCOMES AND BIOMARKERS IN ILD.
Autor:
G. Povysil, J.L. Todd, A.S. Allen, D.F. Dilling, H.J. Kim, M.L. Neely, I. Noth, Z. Ren, L.D. Snyder, M.E. Strek, A. Swaminathan, D. Zhang, C. Hesslinger, T.B. Leonard, D.B. Goldstein, S.M. Palmer, null on behalf of the IPF-PRO Registry investigators
Publikováno v:
D30. THE INJURED LUNG: MECHANISMS AND THERAPEUTIC TARGETS.