Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Shin Yamashiro"'
Publikováno v:
Medicina, Vol 57, Iss 10, p 1121 (2021)
Background and Objectives: Idiopathic pulmonary fibrosis (IPF) has a variable clinical course, which ranges from being asymptomatic to progressive respiratory failure. The purpose of this study was to evaluate the novel clinical parameters of IPF pat
Externí odkaz:
https://doaj.org/article/0cf0ea08088f45c391aa1ee1976cd9a1
Publikováno v:
PLoS ONE, Vol 12, Iss 6, p e0179795 (2017)
Management of severe central airway obstruction due to advanced cancer is a medical and technical challenge. The impact of airway stenting on the clinical outcome of such patients is unclear.This single-center, retrospective study evaluated 21 patien
Externí odkaz:
https://doaj.org/article/2ca97262cd1b40048ca1b8c039ae8cd9
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0186826 (2017)
Nontuberculous mycobacteria (NTM) lung disease is increasing globally. Although the etiological epidemiology of NTM is different across regions, Mycobacterium avium complex (MAC) is the leading cause of NTM lung disease in most countries, including m
Externí odkaz:
https://doaj.org/article/b657a18e6e9e43b884182e7eea684f54
Publikováno v:
Medicina, Vol 57, Iss 1121, p 1121 (2021)
Medicina
Volume 57
Issue 10
Medicina
Volume 57
Issue 10
Background and Objectives: Idiopathic pulmonary fibrosis (IPF) has a variable clinical course, which ranges from being asymptomatic to progressive respiratory failure. The purpose of this study was to evaluate the novel clinical parameters of IPF pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e16a15e693252e7d90dbc8c822dbf7c7
https://www.mdpi.com/1648-9144/57/10/1121
https://www.mdpi.com/1648-9144/57/10/1121
Publikováno v:
The Eurasian Journal of Medicine. 50:6-10
Objective Idiopathic pulmonary fibrosis (IPF) is the most common parenchymal lung disease. Patients with IPF sometimes develop acute exacerbation (AE), which predicts a poor prognosis. To evaluate the predictors of 90-day mortality of AE in patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddd2bdfcd113719374c724955b1f36d7
https://doi.org/10.5152/eurasianjmed.2018.17330
https://doi.org/10.5152/eurasianjmed.2018.17330
Clinical characteristics of idiopathic pulmonary fibrosis patients according to their smoking status
Publikováno v:
Journal of Thoracic Disease. 8:1112-1120
Idiopathic pulmonary fibrosis (IPF) is the most common form of idiopathic interstitial pneumonias (IIPs) of unknown etiology that often affects male, elderly smokers. However, it is sometimes observed in never smokers. This study aimed to clarify the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14d0474b6cdee310201148d72e1390b2
https://doi.org/10.21037/jtd.2016.03.89
https://doi.org/10.21037/jtd.2016.03.89
Autor:
Hiroaki Nagano, Yuichiro Nei, Tomoo Kishaba, Rita L. McGill, Masashi Momose, kenta Nishiyama, Shin Yamashiro, Sachi Ibuki
Publikováno v:
The journal of medical investigation : JMI. 65(3.4)
BACKGROUND Dermatomyositis (DM) and polymyositis (PM) often have association with interstitial lung disease (ILD) which have disease specific autoantibody. METHODOLOGY We reviewed medical records of DM/PM associated ILD from January 2000 to December
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5951b00cdcdaeec1b967181c46d1ccbe
https://pubmed.ncbi.nlm.nih.gov/30282869
https://pubmed.ncbi.nlm.nih.gov/30282869
Publikováno v:
Chest. 154(3)
Case Presentation A 47-year-old man was admitted to the ICU with acute hypercapnic respiratory failure caused by a severe asthma attack. He had a history of asthma, atrial septal defect, chronic heart failure, and atrial fibrillation. He underwent su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a66bf4b38f9bac4a4ac5f5ae69cfea68
https://pubmed.ncbi.nlm.nih.gov/30195374
https://pubmed.ncbi.nlm.nih.gov/30195374
Autor:
Hajime Fukuyama1 fukuyama.hajime.55@gmail.com, Shin Yamashiro1, Kiyoshi Kinjo2, Hitoshi Tamaki1, Tomoo Kishaba1
Publikováno v:
BMC Infectious Diseases. 2014, Vol. 14, p1-8. 8p. 2 Diagrams, 5 Charts.
Autor:
Tomoo Kishaba, Yuichiro Nei, Hiroaki Nagano, Shin Yamashiro, Fumihito Kunishima, Junya Fukuoka
Aims: Fibrotic sarcoidosis is not common presentation and it is not easy to diagnose for many differential diagnosis. We herein report an interesting fibrotic sarcoidosis who shows atypical presentation such as progressive dyspnea with fibrotic imagi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78664f83449847e7c08af94e208f3614
https://zenodo.org/record/821323
https://zenodo.org/record/821323
