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2. Biological Age, Chronological Age, and Survival in Pulmonary Fibrosis: A Causal Mediation Analysis

6. Identification of Molecular Endotypes With Differential Anti-fibrotic Response in Idiopathic Pulmonary Fibrosis: A Latent Class Analysis of Two Multi-center Observational Cohorts

7. Suspected acute exacerbation of idiopathic pulmonary fibrosis as an outcome measure in clinical trials

9. Forced vital capacity trajectories in patients with idiopathic pulmonary fibrosis: a secondary analysis of a multicentre, prospective, observational cohort

10. Effects of interferon-gamma 1b on biomarker expression in patients with idiopathic pulmonary fibrosis

12. Proteomic Determinants of Idiopathic Pulmonary Fibrosis Survival

15. Machine Learning of Plasma Proteomics for Differential Diagnosis of Interstitial Lung Disease

17. Introduction of Home Spirometry in Tracking Disease Progression in Patients With IPF: Baseline Data From the Prospective Treatment Efficacy in IPF Using Genotype for NAC Selection (PRECISIONS) Clinical Trial

19. S109 Genome-wide analysis of longitudinal lung function and gas transfer in individuals with idiopathic pulmonary fibrosis

22. Integrating Gene Expression with Genome-Wide Association Summary Statistics to Identify Genes Associated with Idiopathic Pulmonary Fibrosis Survival

23. Analysis of Forced Vital Capacity (FVC) Trajectories in Idiopathic Pulmonary Fibrosis (IPF) Identifies Four Distinct Clusters of Disease Behaviour

24. Phage Immunoprecipitation Sequencing Defines CDHR5 and GIMAP1 as Novel Biomarkers for a Subset of Fibrotic Pulmonary Disorders

25. Longitudinal lung function and gas transfer in individuals with idiopathic pulmonary fibrosis: a genome-wide association study

26. Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics

27. S63 Genome-wide sex-by-SNP interaction analysis of susceptibility to idiopathic pulmonary fibrosis

28. S65 Genome-wide association study of survival times after diagnosis of idiopathic pulmonary fibrosis

29. The MUC5B rs35705950 Allele Associates with Increased Honeycombing Risk in Individuals of Diverse Ancestry with Pulmonary Fibrosis

34. Detection and Early Referral of Patients With Interstitial Lung Abnormalities: An Expert Survey Initiative

35. Proportion of idiopathic pulmonary fibrosis risk explained by known genetic loci

36. Einleitung - Gleichgeschlechtliche Liebe und die Kirchen : Zum Umgang mit homosexuellen Partnerschaften

37. Ehe und Familie im Wandel – Entwicklungen in Recht und Politik

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

39. Gene Expression Profiling in Patients with Idiopathic Pulmonary Fibrosis (IPF) in the INMARK Trial

41. Association of Circulating Proteins with Death or Lung Transplant in the IPF-PRO Registry Cohort

48. Effect of nintedanib on biomarkers of extracellular matrix (ECM) turnover and FVC decline in patients with IPF: results from the INMARK study*

49. Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis

50. T1 Meta-analysis of idiopathic pulmonary fibrosis genome-wide analyses identifies three novel genetic signals associated with disease susceptibility

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