Pulmonary function testing in idiopathic interstitial pneumonias
about
Classification and natural history of the idiopathic interstitial pneumoniasState of the art in the diagnosis and management of interstitial lung diseasePersonalized medicine: applying 'omics' to lung fibrosisEvolving genomic approaches to idiopathic pulmonary fibrosis: moving beyond genesAltered upper airway and soft tissue structures in the New Zealand Obese mouse.Texture analysis using proton density and T2 relaxation in patients with histological usual interstitial pneumonia (UIP) or nonspecific interstitial pneumonia (NSIP).Influence of sex and disease severity on gene expression profiles in individuals with idiopathic pulmonary fibrosis.Genetics and early detection in idiopathic pulmonary fibrosisPirfenidone treatment of idiopathic pulmonary fibrosis.Micro-mechanical characterization of lung tissue using atomic force microscopy.Quantitative computerized two-point correlation analysis of lung CT scans correlates with pulmonary function in pulmonary sarcoidosisComplex regulation of pulmonary inflammation and fibrosis by CCL18Intersession variability in single-breath diffusing capacity in diabetics without overt lung disease.A Systematic Review of the Role of Dysfunctional Wound Healing in the Pathogenesis and Treatment of Idiopathic Pulmonary Fibrosis.Clinical expert panel on monitoring potential lung toxicity of inhaled oligonucleotides: consensus points and recommendations.Perfusion- and pattern-based quantitative CT indexes using contrast-enhanced dual-energy computed tomography in diffuse interstitial lung disease: relationships with physiologic impairment and prediction of prognosis.Infant pulmonary function testing in chronic pneumonitis of infancy due to surfactant protein C mutation.Epigenetic mechanisms through which Toll-like receptor-9 drives idiopathic pulmonary fibrosis progression.Stretch-induced Activation of Transforming Growth Factor-β1 in Pulmonary Fibrosis.T2 mapping of CT remodelling patterns in interstitial lung disease.Global impairment of CD4+CD25+FOXP3+ regulatory T cells in idiopathic pulmonary fibrosis.
P2860
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P2860
Pulmonary function testing in idiopathic interstitial pneumonias
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Pulmonary function testing in idiopathic interstitial pneumonias
@ast
Pulmonary function testing in idiopathic interstitial pneumonias
@en
type
label
Pulmonary function testing in idiopathic interstitial pneumonias
@ast
Pulmonary function testing in idiopathic interstitial pneumonias
@en
prefLabel
Pulmonary function testing in idiopathic interstitial pneumonias
@ast
Pulmonary function testing in idiopathic interstitial pneumonias
@en
P2860
P1476
Pulmonary function testing in idiopathic interstitial pneumonias
@en
P2093
Fernando J Martinez
Kevin Flaherty
P2860
P304
P356
10.1513/PATS.200602-022TK
P577
2006-06-01T00:00:00Z