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Lung cancer and interstitial lung disease: a literature review
JM Naccache, Q Gibiot, I Monnet… - Journal of thoracic …, 2018 - pmc.ncbi.nlm.nih.gov
The association between lung cancer (LC) and interstitial lung disease (ILD) can be
explained by the shared risk factors like smoking and physiopathology of fibrogenesis and …
explained by the shared risk factors like smoking and physiopathology of fibrogenesis and …
Lung cancer in patients with idiopathic pulmonary fibrosis
T Karampitsakos, V Tzilas, R Tringidou… - Pulmonary …, 2017 - Elsevier
Idiopathic pulmonary fibrosis (IPF) is a chronic fibrotic lung disease of unknown etiology.
With a gradually increasing worldwide prevalence and a mortality rate exceeding that of …
With a gradually increasing worldwide prevalence and a mortality rate exceeding that of …
[HTML][HTML] Definition and assessment of high risk in patients considered for lobectomy for stage I non–small cell lung cancer: The American Association for Thoracic …
Objective Lobectomy is a standard treatment for stage I non–small cell lung cancer, but a
significant proportion of patients are considered at high risk for complications, including …
significant proportion of patients are considered at high risk for complications, including …
Effect of perioperative pirfenidone treatment in lung cancer patients with idiopathic pulmonary fibrosis
T Iwata, S Yoshida, T Fujiwara, H Wada… - The Annals of thoracic …, 2016 - Elsevier
Background Acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF) is a life-
threatening complication of lung cancer operation for patients with IPF, and no effective …
threatening complication of lung cancer operation for patients with IPF, and no effective …
Japanese guidelines for the treatment of idiopathic pulmonary fibrosis 2023: Revised edition
M Bando, S Homma, H Date, K Kishi, H Yamauchi… - Respiratory …, 2024 - Elsevier
Idiopathic pulmonary fibrosis (IPF) is an interstitial lung disease with a poor prognosis and
an unknown cause that generally progresses to pulmonary fibrosis and leads to irreversible …
an unknown cause that generally progresses to pulmonary fibrosis and leads to irreversible …
[HTML][HTML] Lung cancer in patients with fibrosing interstitial lung diseases: an overview of current knowledge and challenges
N Kewalramani, C Machahua, V Poletti… - ERJ open …, 2022 - publications.ersnet.org
Patients with progressive fibrosing interstitial lung diseases (fILD) have increased morbidity
and mortality. Lung fibrosis can be associated with lung cancer. The pathogenesis of both …
and mortality. Lung fibrosis can be associated with lung cancer. The pathogenesis of both …
Recent lessons learned in the management of acute exacerbation of idiopathic pulmonary fibrosis
Y Kondoh, V Cottin, KK Brown - European Respiratory …, 2017 - publications.ersnet.org
Recognising recent advances, the definition and diagnostic criteria for acute exacerbation of
idiopathic pulmonary fibrosis (AE-IPF) have been updated by an international working …
idiopathic pulmonary fibrosis (AE-IPF) have been updated by an international working …
The oncogenic landscape of the idiopathic pulmonary fibrosis: a narrative review
GM Stella, V D'Agnano, D Piloni… - Translational Lung …, 2022 - pmc.ncbi.nlm.nih.gov
Background and Objective Translational research is a source of continuous innovation in
medicine, more particularly for clinical research on new treatment modalities in idiopathic …
medicine, more particularly for clinical research on new treatment modalities in idiopathic …
Management of patients with idiopathic pulmonary fibrosis and lung cancer: challenges in clinical practice
Current Opinion in Pulmonary Medicine Log in or Register Subscribe to journalSubscribe Get
new issue alertsGet alerts Secondary Logo Journal Logo Advanced Search Toggle navigation …
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The clinical impact of major comorbidities on idiopathic pulmonary fibrosis
A Suzuki, Y Kondoh - Respiratory Investigation, 2017 - Elsevier
Idiopathic pulmonary fibrosis (IPF) is a progressive and devastating disease with a median
survival time of 2–3 years after diagnosis. Patients with IPF exhibit distinct patterns of …
survival time of 2–3 years after diagnosis. Patients with IPF exhibit distinct patterns of …