273 results on '"Johkoh, Takeshi"'
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2. Variability of radiological and clinical features in cases with usual interstitial pneumonia without honeycombing
3. Validation of a computed tomography diagnostic model for differentiating fibrotic hypersensitivity pneumonitis from idiopathic pulmonary fibrosis
4. Squamous metaplasia is an indicator of acute exacerbation in patients with usual interstitial pneumonia / idiopathic pulmonary fibrosis
5. A prospective cohort study of periostin as a serum biomarker in patients with idiopathic pulmonary fibrosis treated with nintedanib
6. 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)
7. Japanese guidelines for the treatment of idiopathic pulmonary fibrosis 2023:Revised edition
8. High-resolution CT phenotypes in pulmonary sarcoidosis: a multinational Delphi consensus study
9. Central Bronchial Deformity in Pulmonary Sarcoidosis: A Finding Suggestive of an Upper Lobe Fibrotic Phenotype on Chest Images
10. Japanese clinical practice guide 2022 for hypersensitivity pneumonitis
11. Skeletal muscle atrophy and short-term mortality in patients with acute exacerbation of idiopathic pulmonary fibrosis: an observational cohort study
12. MIXTURE of human expertise and deep learning—developing an explainable model for predicting pathological diagnosis and survival in patients with interstitial lung disease
13. Factors associated with gravity-dependent distribution on chest CT in elderly patients with community-acquired pneumonia: a retrospective observational study
14. Sensitivity of transbronchial lung cryobiopsy in the diagnosis of different interstitial lung diseases
15. Early corticosteroid dose tapering in patients with acute exacerbation of idiopathic pulmonary fibrosis
16. 2020 guide for the diagnosis and treatment of interstitial lung disease associated with connective tissue disease
17. Serial 6-month change in forced vital capacity predicts subsequent decline and mortality in Japanese patients with newly diagnosed idiopathic pulmonary fibrosis
18. Progression of traction bronchiectasis/bronchiolectasis in interstitial lung abnormalities is associated with increased all-cause mortality: Age Gene/Environment Susceptibility-Reykjavik Study
19. Intractable diffuse pulmonary diseases: Manual for diagnosis and treatment
20. Presence of focal usual interstitial pneumonia is a key prognostic factor in progressive pulmonary fibrosis.
21. Interstitial lung abnormalities detected incidentally on CT: a Position Paper from the Fleischner Society
22. Predictive factors for the recurrence of anti-aminoacyl-tRNA synthetase antibody-associated interstitial lung disease
23. Pleuroparenchymal fibroelastosis-like lesions in patients with interstitial pneumonia diagnosed by multidisciplinary discussion with surgical lung biopsy
24. Influenza H1N1 virus-associated pneumonia often resembles rapidly progressive interstitial lung disease seen in collagen vascular diseases and COVID-19 pneumonia; CT-pathologic correlation in 24 patients
25. Usefulness of new diagnostic criteria for chronic hypersensitivity pneumonitis established on the basis of a Delphi survey: A Japanese cohort study
26. Clinical phenotypes from fatal cases of acute respiratory distress syndrome caused by pneumonia
27. High-resolution CT features distinguishing usual interstitial pneumonia pattern in chronic hypersensitivity pneumonitis from those with idiopathic pulmonary fibrosis
28. Prognostic factors for primary Sjögren's syndrome-associated interstitial lung diseases
29. Criteria for the diagnosis of idiopathic pleuroparenchymal fibroelastosis: A proposal
30. Pleuroparenchymal fibroelastosis diagnosed by multidisciplinary discussions in Japan
31. Japanese guideline for the treatment of idiopathic pulmonary fibrosis
32. Radiologic–Pathologic Correlation of Solid Portions on Thin-section CT Images in Lung Adenocarcinoma: A Multicenter Study
33. Distinctive characteristics and prognostic significance of interstitial pneumonia with autoimmune features in patients with chronic fibrosing interstitial pneumonia
34. Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper
35. Idiopathic Pulmonary Fibrosis Incidentally Detected by Computed Tomography Scan as Interstitial Lung Abnormalities.
36. Pleuroparenchymal fibroelastosis-like lesions on chest computed tomography in routine clinical practice
37. Clinical diagnosis of idiopathic pleuroparenchymal fibroelastosis: A retrospective multicenter study
38. Remodeling of the pulmonary artery in idiopathic pleuroparenchymal fibroelastosis
39. Comprehensive assessment of myositis-specific autoantibodies in polymyositis/dermatomyositis-associated interstitial lung disease
40. Pulmonary alveolar proteinosis-like change: A fairly common reaction associated with the severity of idiopathic pulmonary fibrosis
41. Multicentre evaluation of multidisciplinary team meeting agreement on diagnosis in diffuse parenchymal lung disease: a case-cohort study
42. Periostin Is a Biomarker of Rheumatoid Arthritis-Associated Interstitial Lung Disease.
43. Stepwise diagnostic algorithm for high-attenuation pulmonary abnormalities on CT.
44. Pleuroparenchymal fibroelastosis: Distinct pulmonary physiological features in nine patients
45. Broader criteria of undifferentiated connective tissue disease in idiopathic interstitial pneumonias
46. Serum level of periostin can predict long-term outcome of idiopathic pulmonary fibrosis
47. Computed tomographic features of lymphangioleiomyomatosis: Evaluation in 138 patients
48. Rare idiopathic intestinal pneumonias (IIPs) and histologic patterns in new ATS/ERS multidisciplinary classification of the IIPs
49. Clinical Significance of Forced Oscillation Technique for Evaluation of Small Airway Disease in Interstitial Lung Diseases
50. Association Between Baseline Pulmonary Status and Interstitial Lung Disease in Patients With Non–Small-Cell Lung Cancer Treated With Erlotinib—A Cohort Study
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