Results 71 to 80 of about 28,410 (256)

Interpretation of HRCT Scans in the Diagnosis of IPF: Improving Communication Between Pulmonologists and Radiologists. [PDF]

, 2018
Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing interstitial lung disease (ILD). In this review, we describe the central role of high-resolution computed tomography (HRCT) in the diagnosis of IPF and discuss how communication between ...
Chung, Jonathan H, Goldin, Jonathan G
core  

Development and Validation of a Clinical Scoring System Predicting 30‐Day Mortality in Acute Exacerbation of Idiopathic Pulmonary Fibrosis

Respirology, EarlyView.
A scoring system using eight clinical variables was developed and validated to predict 30‐day mortality in acute exacerbation of idiopathic pulmonary fibrosis. The model showed good performance in both derivation and validation cohorts, providing a practical bedside tool for early risk stratification.
Joong‐Yub Kim, Jayoun Kim, Myeong Geun Choi, Min Jee Kim, Yun Hae Ahn, Nakwon Kwak, Jaeyoung Cho, Jinwoo Lee, Young Sik Park, Chang‐Hoon Lee, Sang‐Min Lee, Chul‐Gyu Yoo, Jin Woo Song, Sun Mi Choi   +13 more
wiley   +1 more source

Sequencing of idiopathic pulmonary fibrosis-related genes reveals independent single gene associations [PDF]

, 2014
BACKGROUND: Previous studies investigating a genetic basis for idiopathic pulmonary fibrosis (IPF) have focused on resequencing single genes in IPF kindreds or cohorts to determine the genetic contributions to IPF.
Coghlan, Meghan A, Cole, F. Sessions, Hamvas, Aaron, Huang, Howard J, Mitra, Robi D, Russell, Tonya D, Shifren, Adrian, Wegner, Daniel J, Zhang, Qunyuan   +8 more
core   +3 more sources

Comprehensive gene expression profiling identifies distinct and overlapping transcriptional profiles in non-specific interstitial pneumonia and idiopathic pulmonary fibrosis

Respiratory Research, 2018
Background The clinical-radiographic distinction between idiopathic pulmonary fibrosis (IPF) and non-specific interstitial pneumonia (NSIP) is challenging. We sought to investigate the gene expression profiles of IPF and NSIP vs. normal controls. Methods
Matthew J. Cecchini, Karishma Hosein, Christopher J. Howlett, Mariamma Joseph, Marco Mura   +4 more
doaj   +1 more source

Dyskeratosis Congenita Showing Usual Interstitial Pneumonia.

Internal Medicine, 1994
A 46-year-old man was admitted to our hospital with cough and dyspnea on exertion. A chest X-ray film showed diffuse interstitial shadows. He had hyperpigmentation forming a network pattern around his neck and dystrophy of the fingernails and toenails, and was diagnosed as having dyskeratosis congenita.
Takeshi Yagi, Mikio Toyoshima, Atsushi Yoshitomi, Shiro Imokawa, Hiroshi Hayakawa, Hideki Suganuma, Atsuhiko Sato, Takafumi Suda, Masatoshi Iwata, Kingo Chida, Ryoji Tamura   +10 more
openaire   +4 more sources

Comparison of three groups of patients with usual interstitial pneumonia [PDF]

Respiratory Medicine, 2012
To determine the clinical characteristics and outcomes of patients with lungdominant connective tissue disease (LD-CTD) with a usual interstitial pneumonia (UIP) who do not meet the criteria for any form of CTD, and to compare these parameters with those of patients with idiopathic pulmonary fibrosis (IPF/UIP) and CTD-associated-UIP.We conducted a ...
Ahmad A. Al-Boukai, Emad Raddaoui, Esam H. Alhamad, Shaffi Ahamed Shaik, Feisal A. Al-Kassimi, Waseem Hajjar, M.S. Al-Hajjaj   +6 more
openaire   +3 more sources

Microplastics in Human Bronchoalveolar Lavage Fluid

Respirology, EarlyView.
We established a microplastic detection method using bronchoalveolar lavage fluid. The method detected microplastics, particularly those under 10 μm, in all patients, linked to lung and systemic inflammation. The potential relationship between microplastics and lung and systemic inflammation provides a foundation for larger studies on their health ...
Takatomo Tokito, Takashi Kido, Osamu Nagafuchi, Koichi Tomoshige, Koyomi Nakazawa, Ken'ichi Shinozuka, Shuntaro Sato, Kumiko Kido, Yasuko Noguchi, Takamune Matsumoto, Satoshi Mizoguchi, Ritsuko Murakami, Hirokazu Yura, Hiroshi Ishimoto, Takahiro Takazono, Noriho Sakamoto, Yuji Ishimatsu, Yoshimasa Tanaka, Keitaro Matsumoto, Takeshi Nagayasu, Hiroshi Mukae   +20 more
wiley   +1 more source

Idiopathic pulmonary fibrosis: evaluation of progression and prognosis after the ATS/ERS/JRS/ALAT statement 2011 [PDF]

, 2012
Objectives The prediction of usual interstitial pneumonia (UIP) progression and prognosis by the a application of HRCT criteria pattern recommended by ATS/ERS/JALAT guidelines 2011 Materials and methods Two radiologists after assessing the baseline HRCT ...
ROMEI, CHIARA
core  

Usual interstitial pneumonia [PDF]

, 2019
El patrón histológico de neumonía intersticial usual (NIU) fue descrito por primera vez en 1969 por Averill Liebow como una forma común de fibrosis pulmonar en adultos mayores (1).
Arias Bello, Martha Liliana, Celis-Preciado, Carlos Andrés, Chevalier Chockee, Elena, Galindo, Javier Leonardo, Galindo, Javier Leonardo, Rodríguez Sarmiento, Jorge Luis   +5 more
core   +1 more source

A Case of Combined Sarcoidosis and Usual Interstitial Pneumonia

Internal Medicine, 2012
Sarcoidosis is a systemic granulomatous disease of unknown etiology with characteristic pulmonary lesions, which are often distributed in the upper lung fields. We describe a unique case of sarcoidosis with lower lung field-dominant reticular shadows. Three years after the diagnosis of sarcoidosis based on histologic findings of the mediastinal lymph ...
Tomoko Kagawa, Kazunobu Tachibana, Toru Arai, Masanori Kitaichi, Shojiro Minomo, Yoshikazu Inoue, Masanori Akira   +6 more
openaire   +3 more sources