User profiles for Imre Noth

Imre Noth

Verified email at hscmail.mcc.virginia.edu
Cited by 14110

Acute exacerbations of idiopathic pulmonary fibrosis

…, TE King Jr, JA Lasky, JE Loyd, I Noth… - American journal of …, 2007 - atsjournals.org
The natural history of idiopathic pulmonary fibrosis (IPF) has been characterized as a steady,
predictable decline in lung function over time. Recent evidence suggests that some …

An official European Respiratory Society/American Thoracic Society research statement: interstitial pneumonia with autoimmune features

…, EL Matteson, M Mosca, I Noth… - European …, 2015 - Eur Respiratory Soc
Many patients with an idiopathic interstitial pneumonia (IIP) have clinical features that suggest
an underlying autoimmune process but do not meet established criteria for a connective …

Lung microbiome and disease progression in idiopathic pulmonary fibrosis: an analysis of the COMET study

MLK Han, Y Zhou, S Murray, N Tayob, I Noth… - The Lancet …, 2014 - thelancet.com
Background The role of the lung microbiome in the pathogenesis of idiopathic pulmonary
fibrosis is unknown. We investigated whether unique microbial signatures were associated …

TOLLIP, MUC5B, and the Response to N-Acetylcysteine among Individuals with Idiopathic Pulmonary Fibrosis

…, C Lee, R Vij, Y Huang, ME Strek, I Noth - American journal of …, 2015 - atsjournals.org
Rationale: Idiopathic pulmonary fibrosis (IPF) is a devastating lung disease of unknown
etiology. The genes TOLLIP and MUC5B play important roles in lung host defense, which is an …

Peripheral blood mononuclear cell gene expression profiles predict poor outcome in idiopathic pulmonary fibrosis

JD Herazo-Maya, I Noth, SR Duncan, SH Kim… - Science translational …, 2013 - science.org
We aimed to identify peripheral blood mononuclear cell (PBMC) gene expression profiles
predictive of poor outcomes in idiopathic pulmonary fibrosis (IPF) by performing microarray …

Genome-wide association study of susceptibility to idiopathic pulmonary fibrosis

…, PL Molyneaux, C Flores, I Noth… - American journal of …, 2020 - atsjournals.org
Rationale: Idiopathic pulmonary fibrosis (IPF) is a complex lung disease characterized by
scarring of the lung that is believed to result from an atypical response to injury of the …

Circulating plasma biomarkers of survival in antifibrotic-treated patients with idiopathic pulmonary fibrosis

…, SF Ma, A Haczku, A Sperling, ME Strek, I Noth… - Chest, 2020 - Elsevier
Background A number of circulating plasma biomarkers have been shown to predict survival
in patients with idiopathic pulmonary fibrosis (IPF), but most were identified before the use …

Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study

I Noth, Y Zhang, SF Ma, C Flores, M Barber… - The Lancet respiratory …, 2013 - thelancet.com
Background Idiopathic pulmonary fibrosis (IPF) is a devastating disease that probably
involves several genetic loci. Several rare genetic variants and one common single nucleotide …

A placebo-controlled randomized trial of warfarin in idiopathic pulmonary fibrosis

I Noth, KJ Anstrom, SB Calvert… - American journal of …, 2012 - atsjournals.org
Rationale: Animal and human studies support the importance of the coagulation cascade in
pulmonary fibrosis. Objectives: In a cohort of subjects with progressive idiopathic pulmonary …

Churg-strauss syndrome

I Noth, ME Strek, AR Leff - The Lancet, 2003 - thelancet.com
Churg-Strauss syndrome is a rare diffuse vasculitis that is almost invariably accompanied by
severe asthma. Although overall prognosis is good, and treatment with prednisone alone or …