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1. The COPD assessment test and St George's Respiratory Questionnaire: are they equivalent in subjects with COPD?

2. Using Imaging to Predict, Identify, and Monitor Progression of Interstitial Lung Disease: Consensus Findings From a Modified Delphi Study

4. Analysis of Early Intervention of Nintedanib After Antiinflammatory Treatment in Patients With Non-idiopathic Pulmonary Fibrosis Fibrotic Interstitial Lung Disease: A Single Center Retrospective Study in Japan

5. How Should Patients With Progressive Pulmonary Fibrosis Be Identified? Consensus Findings From a Modified Delphi Study

6. Nintedanib in patients with progressive fibrosing interstitial lung diseases—subgroup analyses by interstitial lung disease diagnosis in the INBUILD trial: a randomised, double-blind, placebo-controlled, parallel-group trial

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

10. Nationwide prospective registry of idiopathic interstitial pneumonias with central multidisciplinary diagnosis in Japan (JIPS Registry): Analysis of disease progression

14. Nintedanib for Systemic Sclerosis-Associated Interstitial Lung Disease

16. Analysis of Serum Angiopoietin-1 and -2 Concentrations in Patients with Pulmonary Hypertension

17. The Local Structure and Metal-Insulator Transition in a Ba 3 Nb 5−x Ti x O 15 System.

18. Acute exacerbation of idiopathic pulmonary fibrosis: International survey and call for harmonisation

19. Acute exacerbation of idiopathic pulmonary fibrosis

20. Nintedanib in patients with progressive fibrosing interstitial lung diseases—subgroup analyses by interstitial lung disease diagnosis in the INBUILD trial: a randomised, double-blind, placebo-controlled, parallel-group trial

22. Efficacité et tolérance du nintédanib chez des patients atteints de pneumopathie interstitielle diffuse associée à la sclérodermie systémique (SSc-PID) en fonction de l’indice de masse corporelle (IMC) à l’inclusion : analyse en sous-groupes de l’étude SENSCIS

24. Le taux de déclin de la fonction pulmonaire est-il le même chez les patients atteints d’une pneumopathie interstitielle diffuse associée à la sclérodermie systémique (PID-ScS) qui présentent une perte de poids ? Données de l’étude SENSCIS

25. Thermochemical hydrogen production by a redox system of Zr[O.sub.2]-supported Co(II)-ferrite

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

29. SAT0329 IS THE RATE OF LUNG FUNCTION DECLINE THE SAME IN PATIENTS WITH SYSTEMIC SCLEROSIS-ASSOCIATED ILD (SSC-ILD) WHO EXPERIENCE WEIGHT LOSS? DATA FROM THE SENSCIS TRIAL

30. Pirfenidone Delays the Prescription of Concomitant Drugs in Patients with Idiopathic Pulmonary Fibrosis: Post-Hoc Analysis of Japanese Phase III Clinical Trial

31. Nintedanib in patients with progressive fibrosing interstitial lung diseases—subgroup analyses by interstitial lung disease diagnosis in the INBUILD trial: a randomised, double-blind, placebo-controlled, parallel-group trial

32. Prognostic Heterogeneity in Patients with Idiopathic Pulmonary Fibrosis Based on Disease Behavior

33. The Relationship Between Single-Nucleotide Polymorphisms Within Tollip and the Efficacy of Inhaled N-Acetylcysteine Therapy in Idiopathic Pulmonary Fibrosis.

34. A Prospective Randomized, Multicenter Trial Evaluating the Efficacy and Safety of Combined Therapy with Pirfenidone and Inhaled N-Acetylcysteine for Idiopathic Pulmonary Fibrosis

41. Identification of a chemical modulator of EZH2-mediated silencing by cell-based high-throughput screening assay

45. Diagnostic likelihood thresholds that define a working diagnosis of idiopathic pulmonary fibrosis

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