Zobrazeno 1 - 10
of 862
pro vyhledávání: '"nonspecific interstitial pneumonia"'
Akademický článek
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Autor:
Naoko Arakawa, Yuno Shiota, Fumi Onizawa, Fumi Miyata, Azusa Miyoshi, Tomohiro Akaba, Mayoko Tsuji, Ken Arimura, Osamitsu Yagi, Mitsuko Kondo, Hideki Katsura, Etsuko Tagaya
Publikováno v:
Respirology Case Reports, Vol 12, Iss 6, Pp n/a-n/a (2024)
Abstract A 46‐year‐old male was treated with corticosteroids for nonspecific interstitial pneumonia (NSIP). He was referred to our hospital and admitted for worsening dyspnea and diffuse ground‐glass opacity on chest computed tomography (CT) du
Externí odkaz:
https://doaj.org/article/fb7a3d654b0145849fb1cf777563714a
Autor:
Malik A. Althobiani, Anne-Marie Russell, Joseph Jacob, Yatharth Ranjan, Amos A. Folarin, John R. Hurst, Joanna C. Porter
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
Interstitial lung diseases (ILDs) refer to a heterogeneous and complex group of conditions characterized by inflammation, fibrosis, or both, in the interstitium of the lungs. This results in impaired gas exchange, leading to a worsening of respirator
Externí odkaz:
https://doaj.org/article/f28a88a69cf94dfda5f04eac6270adb6
Publikováno v:
Lung India, Vol 41, Iss 3, Pp 172-175 (2023)
Rationale: Nonspecific interstitial pneumonia (NSIP) is a subtype of interstitial lung disease which can either be idiopathic or secondary to other conditions. Idiopathic NSIP is a relatively rare entity and diagnosis should be considered carefully a
Externí odkaz:
https://doaj.org/article/414ae955216b4732a2ab0d3b35a8f9b4
Autor:
Stefano Lucà, Francesca Pagliuca, Fabio Perrotta, Andrea Ronchi, Domenica Francesca Mariniello, Giovanni Natale, Andrea Bianco, Alfonso Fiorelli, Marina Accardo, Renato Franco
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 7, p 3618 (2024)
Idiopathic Interstitial Pneumonias (IIPs) are a heterogeneous group of the broader category of Interstitial Lung Diseases (ILDs), pathologically characterized by the distortion of lung parenchyma by interstitial inflammation and/or fibrosis. The Amer
Externí odkaz:
https://doaj.org/article/26f16d556c1f471cb33bf669c70229f3
Autor:
Raju S. R. Adduri, Kai Cai, Karen Velasco‐Alzate, Ravikiran Vasireddy, Jeffrey W. Miller, Sergio Poli deFrías, Fernando Poli deFrías, Yasushi Horimasu, Hiroshi Iwamoto, Noboru Hattori, Yingze Zhang, Kevin F. Gibson, Anoop K. Pal, Zhe Chen, Daniela Nicastro, Li Li, Sujith Cherian, Lynette M. Sholl, Sreerama Shetty, Harrison Ndetan, Anthony H. Maeda, Maria A. Planchart Ferretto, Gary M. Hunninghake, David A. Schwartz, Daniel J. Kass, Ivan O. Rosas, Nagarjun V. Konduru
Publikováno v:
Journal of Extracellular Biology, Vol 2, Iss 7, Pp n/a-n/a (2023)
Abstract High‐resolution computed tomography (HRCT) imaging is critical for diagnostic evaluation of Idiopathic Pulmonary Fibrosis (IPF). However, several other interstitial lung diseases (ILDs) often exhibit radiologic pattern similar to IPF on HR
Externí odkaz:
https://doaj.org/article/e69d46450fac495195f0f07fb72f96a3
Publikováno v:
Journal of Advanced Lung Health, Vol 3, Iss 3, Pp 117-119 (2023)
Bronchiolocentric interstitial pneumonia is a unique entity with few cases reported in the literature. It is characterized by the pattern of bronchiolocentric injury to the lung in the absence of known causes and its clinical presentation may mimic n
Externí odkaz:
https://doaj.org/article/9841e46564874815b168ce484e13422b
Autor:
Anastasia D. Strutynskaya, Maria A. Karnaushkina, Dmitriy Y. Ovsyannikov, Sergey A. Filippov, Igor E. Tyurin
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 50, Iss 2, Pp 127-132 (2022)
Adult Still's disease is a rare systemic disorder of unknown etiology. Its course is often complicated by interstitial pneumonia and fulminant hepatitis. Published data have indicated some common mechanisms of systemic inflammation in patients with a
Externí odkaz:
https://doaj.org/article/e00c5dc4db584604a103ac00fe11cabf
Autor:
Takashi Higuchi, Shomi Oka, Hiroshi Furukawa, Kota Shimada, Shinichiro Tsunoda, Satoshi Ito, Akira Okamoto, Misuzu Fujimori, Tadashi Nakamura, Masao Katayama, Koichiro Saisho, Satoshi Shinohara, Toshihiro Matsui, Kiyoshi Migita, Shouhei Nagaoka, Shigeto Tohma
Publikováno v:
Genes, Vol 14, Iss 11, p 2084 (2023)
Interstitial lung disease and airway disease (AD) are often complicated with rheumatoid arthritis (RA) and have a poor prognosis. Several studies reported genetic associations with interstitial lung disease in RA. However, few genetic studies have ex
Externí odkaz:
https://doaj.org/article/ad30d7b2a6464206b3771edbb065322a
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.