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

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

7. 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)

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)

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

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

21. 2020 guide for the diagnosis and treatment of interstitial lung disease associated with connective tissue disease

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

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

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

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

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

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

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

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

42. 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)

45. Japanese guideline for the treatment of idiopathic pulmonary fibrosis

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

47. Distinctive characteristics and prognostic significance of interstitial pneumonia with autoimmune features in patients with chronic fibrosing interstitial pneumonia

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

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

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