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1. Artificial Intelligence-based Decision Support for HRCT Stratification in Fibrotic Lung Disease: An International Study of 195 Observers From 43 Countries

3. Usability of a Smartphone Application for Patients With Interstitial Lung Disease (ILD): Early Results From the Registry for Better Understanding of ILD (RE-BUILD) Pilot Study

4. Mapping EQ5D Utilities From Forced Vital Capacity and Diffusing Capacity in Fibrotic Interstitial Lung Disease

5. Ziritaxestat, a novel autotaxin inhibitor, and lung function in idiopathic pulmonary fibrosis

6. Quantitative computed tomography predicts outcomes in idiopathic pulmonary fibrosis

9. The impact of stapling technique and surgeon specialism on anastomotic failure after right-sided colorectal resection: an international multicentre, prospective audit

11. Patients with Crohn's disease have longer post-operative in-hospital stay than patients with colon cancer but no difference in complications' rate

12. Effect of nintedanib in patients with limited and extensive systemic sclerosis-associated interstitial lung disease (SSc-ILD): data from the SENSCIS trial

14. Peer Connect Service for people with pulmonary fibrosis in Australia: Participants' experiences and process evaluation

15. Investigation burden for patients with fibrotic interstitial lung disease at the end of life

16. Diagnostic accuracy of a clinical diagnosis of idiopathic pulmonary fibrosis: an international case-cohort study

19. A Unique Biomarker Signature for Progressive Idiopathic Pulmonary Fibrosis

20. Validation of Deep Learning-Based Diagnostic Likelihoods of Usual Interstitial Pneumonia on Baseline Computed Tomography in the Australian IPF Registry

22. A Unique Biomarker Signature for Progressive Idiopathic Pulmonary Fibrosis

23. Deep Learning-Based Prediction of Progressive Fibrotic Lung Disease on Baseline Computed Tomography in the Australian IPF Registry

24. Quantitative Assessment of Baseline Computed Tomography in the Australian IPF Registry

25. Risk factors for unfavourable postoperative outcome in patients with Crohn's disease undergoing right hemicolectomy or ileocaecal resection. An international audit by ESCP and S-ECCO

29. PD-L1- and calcitriol-dependent liposomal antigen-specific regulation of systemic inflammatory autoimmune disease.

30. Implications of the diagnostic criteria of idiopathic pulmonary fibrosis in clinical practice: Analysis from the Australian Idiopathic Pulmonary Fibrosis Registry

33. Relationship between method of anastomosis and anastomotic failure after right hemicolectomy and ileo-caecal resection : an international snapshot audit

36. Blood Monocyte Count as a Prognostic Marker in Idiopathic Pulmonary Fibrosis: An Australian IPF Registry Analysis

38. Effectiveness of Ultrasound-guided versus Anatomical Landmark-guided Genicular Nerve Block to Treat Chronic Knee Osteoarthritis: A Retrospective Cohort Study

39. 'Baseline characteristics of idiopathic pulmonary fibrosis: analysis from the Australian Idiopathic Pulmonary Fibrosis Registry.' Helen E. Jo, Ian Glaspole, Christopher Grainge, Nicole Goh, Peter M.A. Hopkins, Yuben Moodley, Paul N. Reynolds, Sally Chapman, E. Haydn Walters, Christopher Zappala, Heather Allan, Gregory J. Keir, Andrew Hayen, Wendy A. Cooper, Annabelle M. Mahar, Samantha Ellis, Sacha Macansh and Tamera J. Corte. Eur Respir J 2017; 49: 1651592

40. Baseline characteristics of idiopathic pulmonary fibrosis: Analysis from the Australian Idiopathic Pulmonary Fibrosis Registry

41. Baseline characteristics of idiopathic pulmonary fibrosis: Analysis from the Australian Idiopathic Pulmonary Fibrosis Registry

43. Macitentan for the treatment of idiopathic pulmonary fibrosis: the randomised controlled MUSIC trial

45. Serial change in PFTS is predictive of outcome in systemic sclerosis associated interstitial lung disease.

46. Quantifying change in pulmonary function as a prognostic marker in systemic sclerosis-related interstitial lung disease.

47. Use of Modified Laboratory Instruction for Improving Science Process Skills Acquisition.

49. Quantifying change in pulmonary function as a prognostic marker in systemic sclerosis-related interstitial lung disease.

50. Extent of disease on high-resolution CT lung is a predictor of decline and mortality in systemic sclerosis-related interstitial lung disease.

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