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44 results on '"Morisset J"'

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1. Using Latent Class Analysis to Predict Outcomes and Inform Disease Classification in Fibrotic Interstitial Lung Disease

2. Significance of Cysts in the Diagnosis of Fibrotic Interstitial Lung Disease

3. POS0123 ASSOCIATION OF LUNG IMAGING PATTERN WITH PROGNOSIS AND IMMUNOSUPPRESSION RESPONSE IN CONNECTIVE TISSUE DISEASE ASSOCIATED INTERSTITIAL LUNG DISEASE

4. POS1242 COMPUTED TOMOGRAPHY FINDINGS IN CONNECTIVE TISSUE DISEASE RELATED INTERSTITIAL LUNG DISEASE

5. Clinical and Radiographic Characterization of Non-specific Interstitial Pneumonia on High-resolution CT Chest Imaging

7. Increasing Honeycombing and Traction Bronchiectasis on Computed Tomography Are Independent Predictors of Survival Across All Interstitial Lung Disease Subtypes

8. Bronchoalveolar Lavage Fluid and Radiographic Patterns in Patients With Fibrotic Interstitial Lung Disease

9. Organic and Inorganic Exposures Are Associated With Radiologic Features in Patients With Fibrotic Interstitial Lung Disease

10. Computed Tomography Features Influencing Guideline-defined Radiologic Patterns In Interstitial Lung Disease

11. Radiologic Patterns and Leading Clinical Diagnoses in Unclassifiable Interstitial Lung Disease

12. Clinical and Radiographic Predictors of Mortality or Transplant in Patients With Idiopathic Pulmonary Fibrosis

13. The Clinical Frailty Scale Is Associated With Mortality in Patients With Fibrotic Interstitial Lung Disease - A Multicenter Cohort Study

21. Understanding the Decision-Making Process of the Multidisciplinary Approach for the Diagnosis of Interstitial Lung Disease: A Qualitative Study

22. Inhalational Exposures and Fibrotic Interstitial Lung Disease: Presentation, Prevalence, and Survival in the Canadian Registry for Pulmonary Fibrosis

23. Effect of Smoking Status on Interstitial Lung Disease: Novel Insights from the Prospective Canadian Registry for Pulmonary Fibrosis

24. Prevalence and Characteristics of Progressive Fibrosing Interstitial Lung Disease: Results from the Prospective Canadian Registry for Pulmonary Fibrosis

25. Tolerability of Mycophenolate and Azathioprine in Patients with Fibrotic Interstitial Lung Disease: A Prospective Cohort Study Using Real-World Data

26. Sex Based Differences in the Treatment of Interstitial Lung Diseases in Canada

27. Malignancy Risk Associated with Mycophenolate Mofetil and Azathioprine in Patients with Fibrotic Interstitial Lung Disease

28. 'Real World' Therapeutic Approach and Associations with FVC Decline in IPF Patients Treated with Antifibrotics

29. Association of Body Mass Index and Change in Weight with Mortality in Patients with Fibrotic Interstitial Lung Disease

30. The Impact of Pulmonary Hypertension on Outcomes in Interstitial Lung Disease in a Large Canadian Cohort

31. Change in 6-Minute Walk Distance During in- and Outpatient Pulmonary Rehabilitation Is Associated with Improved Survival in Patients with Fibrotic Interstitial Lung Disease

32. Evaluating the Association of Comorbidity Clusters in Fibrotic Interstitial Lung Disease

34. Predicting New-Onset Exertional Hypoxemia in Interstitial Lung Disease

36. Differences in the Approach to Acute Exacerbation of Idiopathic Pulmonary Fibrosis (AE IPF) Between Expert Centres and General Pulmonologists: Results from an International Survey

37. Minimally Important Difference (MID) for the European Quality of Life - 5 Dimensions (EQ-5D) in Fibrotic Interstitial Lung Disease

39. Impact of a Regional Multidisciplinary Conference on the Diagnosis of Interstitial Lung Disease

41. Disparities in the Treatment of Patients with Interstitial Lung Disease in Canada

42. Derivation and Validation of a Diagnostic Prediction Model for Interstitial Lung Disease

44. Ein globaler Blick auf akute Exazerbationen der idiopathischen Lungenfibrose (AE-IPF): Ergebnisse einer internationalen Umfrage

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