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Respiratory Medicine|July 9, 2013
CCL18 in serum, BAL fluid and alveolar macrophage culture supernatant in interstitial lung diseasesMiaotian Cai, Francesco Bonella, Xuan He, et al.Journal of Clinical Medicine|February 11, 2023
Serum KL-6 as a Biomarker of Progression at Any Time in Fibrotic Interstitial Lung DiseaseLutz B Jehn, Ulrich Costabel, Eda Boerner, et al.Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG|April 9, 2016
Pulmonary alveolar proteinosis: another autoimmune disease associated with sarcoidosis?Eda Burcu Boerner, Ulrich Costabel, Thomas Ernst Wessendorf, et al.Orphanet Journal of Rare Diseases|February 28, 2021
Potential clinical utility of MUC5B und TOLLIP single nucleotide polymorphisms (SNPs) in the management of patients with IPFFrancesco Bonella, Ilaria Campo, Michele Zorzetto, et al.Immunobiology|August 23, 2022
IL-9 and IL-9 receptor expression in lymphocytes from bronchoalveolar lavage fluid of patients with interstitial lung diseaseLutz B Jehn, Ulrich Costabel, Eda Boerner, et al.The European Respiratory Journal|November 13, 2016
Serum YKL-40 as predictor of outcome in hypersensitivity pneumonitisXiaoping Long, Xuan He, Shinichiro Ohshimo, et al.Orphanet Journal of Rare Diseases|April 25, 2016
MUC1 gene polymorphisms are associated with serum KL-6 levels and pulmonary dysfunction in pulmonary alveolar proteinosisFrancesco Bonella, Xiaoping Long, Shinichiro Ohshimo, et al.Respirology (Carlton, Vic.)|January 13, 2015
MUC5B promoter polymorphism in Japanese patients with idiopathic pulmonary fibrosisYasushi Horimasu, Shinichiro Ohshimo, Francesco Bonella, et al.Respiratory Medicine|May 22, 2025
Recurrent pulmonary alveolar proteinosis after lung transplantation: a case seriesDirk Westhölter, Marcel Opitz, Josefine Rawitzer, et al.Thorax|October 7, 2016
Effect of statins on disease-related outcomes in patients with idiopathic pulmonary fibrosisMichael Kreuter, Francesco Bonella, Toby M Maher, et al.Pageof 28