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2. A prospective cohort study of periostin as a serum biomarker in patients with idiopathic pulmonary fibrosis treated with nintedanib

4. Clinical efficacy and safety of multipotent adult progenitor cells (invimestrocel) for acute respiratory distress syndrome (ARDS) caused by pneumonia: a randomized, open-label, standard therapy–controlled, phase 2 multicenter study (ONE-BRIDGE)

8. Validation of a computed tomography diagnostic model for differentiating fibrotic hypersensitivity pneumonitis from idiopathic pulmonary fibrosis

10. High-resolution CT phenotypes in pulmonary sarcoidosis: a multinational Delphi consensus study

14. Updated guidance on the management of COVID-19: from an American Thoracic Society/European Respiratory Society coordinated International Task Force (29 July 2020)

16. Idiopathic Pulmonary Fibrosis Incidentally Detected by CT Scan as Interstitial Lung Abnormalities

18. Sensitivity of transbronchial lung cryobiopsy in the diagnosis of different interstitial lung diseases

21. Presence of focal usual interstitial pneumonia is a key prognostic factor in progressive pulmonary fibrosis.

22. 2020 guide for the diagnosis and treatment of interstitial lung disease associated with connective tissue disease

25. Progression of traction bronchiectasis/bronchiolectasis in interstitial lung abnormalities is associated with increased all-cause mortality: Age Gene/Environment Susceptibility-Reykjavik Study

28. Interstitial lung abnormalities detected incidentally on CT: a Position Paper from the Fleischner Society

33. Periostin Is a Biomarker of Rheumatoid Arthritis-Associated Interstitial Lung Disease

35. “Bull’s-Eye” Sign and Its Longitudinal Change on HRCT in Pulmonary Sarcoidosis

37. Diagnostic Criteria Arrangement in Nationwide All ILD Registry with Central MDD in Japan; PROMISE study

38. Preclinical idiopathic pulmonary fibrosis (IPF): a retrospective cohort study

39. Early intervention of antifibrotics along with anti-inflammatory treatment in rapidly progressive interstitial lung disease (RP-ILD) with anti-MDA5 antibody-positive dermatomyositis (MDA5-DM)

40. Idiopathic Pulmonary Fibrosis Incidentally Detected by Computed Tomography Scan as Interstitial Lung Abnormalities.

42. High-resolution CT features distinguishing usual interstitial pneumonia pattern in chronic hypersensitivity pneumonitis from those with idiopathic pulmonary fibrosis

45. Changes in patient-reported outcomes in patients with non-idiopathic pulmonary fibrosis fibrotic interstitial lung disease and progressive pulmonary fibrosis

47. An Official American Thoracic Society/European Respiratory Society Statement: Update of the International Multidisciplinary Classification of the Idiopathic Interstitial Pneumonias

49. Japanese guideline for the treatment of idiopathic pulmonary fibrosis

50. Radiologic–Pathologic Correlation of Solid Portions on Thin-section CT Images in Lung Adenocarcinoma: A Multicenter Study

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