Reference health
An Official American Thoracic Society/European Respiratory Society Statement: Update of the International Multidisciplinary Classification of the Idiopathic Interstitial Pneumonias
158/158 checkable references clean · checked 2026-07-25
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
7 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 158 checked references that resolve
resolves10.1164/ajrccm.165.2.ats01
American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias
resolves10.1136/thx.2003.020396
HRCT diagnosis of diffuse parenchymal lung disease: inter-observer variation
resolves10.1136/thx.2003.011734
Inter-observer variation between pathologists in diffuse parenchymal lung disease
resolves10.1183/09031936.00063706
Multidisciplinary interobserver agreement in the diagnosis of idiopathic pulmonary fibrosis
resolves10.1164/rccm.2009-040GL
An Official ATS/ERS/JRS/ALAT Statement: Idiopathic Pulmonary Fibrosis: Evidence-based Guidelines for Diagnosis and Management
resolves10.2214/ajr.165.4.7676971
Can CT distinguish hypersensitivity pneumonitis from idiopathic pulmonary fibrosis?
resolves10.2214/AJR.05.1826
Hypersensitivity Pneumonitis: Spectrum of High-Resolution CT and Pathologic Findings
resolves10.1148/radiol.2453061881
Chronic Hypersensitivity Pneumonitis: Differentiation from Idiopathic Pulmonary Fibrosis and Nonspecific Interstitial Pneumonia by Using Thin-Section CT
resolves10.1309/AJCPNWX4SLZRP9SW
Histopathologic Analysis of Sixteen Autopsy Cases of Chronic Hypersensitivity Pneumonitis and Comparison With Idiopathic Pulmonary Fibrosis/Usual Interstitial Pneumonia
resolves10.1097/PAS.0b013e3181bb2538
Pathologic Patterns and Survival in Chronic Hypersensitivity Pneumonitis
resolves10.1016/S1081-1206(10)60573-X
Hypersensitivity pneumonitis as a cause of airway-centered interstitial fibrosis
resolves10.1148/radiol.2442060640
Chronic Hypersensitivity Pneumonitis: CT Features—Comparison with Pathologic Evidence of Fibrosis and Survival
resolves10.4065/82.7.812
Causes and Presenting Features in 85 Consecutive Patients With Hypersensitivity Pneumonitis
resolves10.1007/s00408-006-0104-2
Idiopathic and Collagen Vascular Disease Nonspecific Interstitial Pneumonia: Clinical Significance of Remodeling Process
resolves10.1097/RCT.0b013e318181d551
Computed Tomographic Features of Idiopathic Fibrosing Interstitial Pneumonia
resolves10.1378/chest.08-2572
Pathologic and Radiologic Differences Between Idiopathic and Collagen Vascular Disease-Related Usual Interstitial Pneumonia
resolves10.1183/09031936.00174910
Significance of connective tissue disease features in idiopathic interstitial pneumonia
resolves10.1016/j.rmed.2010.04.022
Distinct prognosis of idiopathic nonspecific interstitial pneumonia (NSIP) fulfilling criteria for undifferentiated connective tissue disease (UCTD)
resolves10.1016/j.rmed.2011.08.022
Familial pulmonary fibrosis is the strongest risk factor for idiopathic pulmonary fibrosis
resolves10.1136/thorax.57.4.338
Nationwide prevalence of sporadic and familial idiopathic pulmonary fibrosis: evidence of founder effect among multiplex families in Finland
resolves10.1136/thorax.55.2.143
Adult familial cryptogenic fibrosing alveolitis in the United Kingdom
resolves10.1056/NEJM200102223440805
A Mutation in the Surfactant Protein C Gene Associated with Familial Interstitial Lung Disease
resolves10.1164/rccm.200906-0953OC
Surfactant Protein C Mutations Are the Basis of a Significant Portion of Adult Familial Pulmonary Fibrosis in a Dutch Cohort
resolves10.1152/ajplung.00382.2007
Endoplasmic reticulum stress in alveolar epithelial cells is prominent in IPF: association with altered surfactant protein processing and herpesvirus infection
resolves10.1056/NEJMc1013504
A Variant in the Promoter of
<i>MUC5B</i>
and Idiopathic Pulmonary Fibrosis
resolves10.1097/MAJ.0b013e31821a9d7a
Genetics in Pulmonary Fibrosis—Familial Cases Provide Clues to the Pathogenesis of Idiopathic Pulmonary Fibrosis
resolves10.1378/chest.125.2.522
Prognostic Implications of Histologic Patterns in Multiple Surgical Lung Biopsies From Patients With Idiopathic Interstitial Pneumonias
resolves10.1378/chest.124.4.1199
The Overlap Between Respiratory Bronchiolitis and Desquamative Interstitial Pneumonia in Pulmonary Langerhans Cell Histiocytosis
resolves10.1183/09031936.00038709
Pulmonary hypertension in patients with combined pulmonary fibrosis and emphysema syndrome
resolves10.1183/09031936.05.00021005
Combined pulmonary fibrosis and emphysema: a distinct underrecognised entity
resolves10.1148/radiol.2511080917
Usual Interstitial Pneumonia and Nonspecific Interstitial Pneumonia with and without Concurrent Emphysema: Thin-Section CT Findings
resolves10.1164/ajrccm.164.9.2103074
Histopathologic Variability in Usual and Nonspecific Interstitial Pneumonias
resolves10.1136/thorax.58.2.143
Radiological versus histological diagnosis in UIP and NSIP: survival implications
resolves10.1148/radiol.0990898
Biopsy-proved Idiopathic Pulmonary Fibrosis: Spectrum of Nondiagnostic Thin-Section CT Diagnoses
resolves10.1164/rccm.200611-1696OC
Computed Tomography Findings in Pathological Usual Interstitial Pneumonia
resolves10.1148/radiol.2471070369
Nonspecific Interstitial Pneumonia and Idiopathic Pulmonary Fibrosis: Changes in Pattern and Distribution of Disease over Time
resolves10.1164/rccm.200412-1756OC
High-Resolution Computed Tomography in Idiopathic Pulmonary Fibrosis
resolves10.2214/ajr.173.4.10511155
Nonspecific interstitial pneumonia with fibrosis: serial high-resolution CT findings with functional correlation.
resolves10.1148/radiology.217.3.r00nv31701
Nonspecific Interstitial Pneumonia: Variable Appearance at High-Resolution Chest CT
resolves10.1148/radiology.195.3.7753988
Nonspecific interstitial pneumonia with fibrosis: radiographic and CT findings in seven patients.
resolves10.1164/ajrccm.158.4.9802119
Nonspecific Interstitial Pneumonia: Individualization of a Clinicopathologic Entity in a Series of 12 Patients
resolves10.1183/09031936.98.12051010
Idiopathic nonspecific interstitial pneumonia/fibrosis: comparison with idiopathic pulmonary fibrosis and BOOP
resolves10.1148/radiol.2251011555
Nonspecific Interstitial Pneumonia: Correlation between Thin-Section CT Findings and Pathologic Subgroups in 55 Patients
resolves10.1148/radiology.211.2.r99ma01555
Idiopathic Interstitial Pneumonias: Diagnostic Accuracy of Thin-Section CT in 129 Patients
resolves10.1097/00004728-200001000-00008
Serial High Resolution CT Findings in Nonspecific Interstitial Pneumonia/Fibrosis
resolves10.1148/radiol.2213010158
Nonspecific Interstitial Pneumonia and Usual Interstitial Pneumonia: Comparative Appearances at and Diagnostic Accuracy of Thin-Section CT
resolves10.1136/thx.2010.140574
Long-term follow-up high-resolution CT findings in non-specific interstitial pneumonia
resolves10.1097/00000478-200001000-00003
Idiopathic Nonspecific Interstitial Pneumonia: Prognostic Significance of Cellular and Fibrosing Patterns
resolves10.1097/01.rct.0000182853.90520.84
Pathologic Subgroups of Nonspecific Interstitial Pneumonia
resolves10.1183/09031936.00158507
Clinical course and lung function change of idiopathic nonspecific interstitial pneumonia
resolves10.1007/s00330-006-0340-0
Smoking-related interstitial lung diseases: radiologic-pathologic correlation
resolves10.1111/j.1365-2559.2004.01921.x
Desquamative interstitial pneumonia, respiratory bronchiolitis and their relationship to smoking
resolves10.1136/thx.2007.083766
Clinical, radiological and pathological features of ABCA3 mutations in children
resolves10.1164/rccm.200503-504OC
<i>ABCA3</i>
Mutations Associated with Pediatric Interstitial Lung Disease
resolves10.1111/j.1365-2559.2008.03183.x
Smoking‐related changes in the background lung of specimens resected for lung cancer: a semiquantitative study with correlation to postoperative course
resolves10.1016/j.humpath.2009.09.003
Clinically occult interstitial fibrosis in smokers: classification and significance of a surprisingly common finding in lobectomy specimens
resolves10.2214/AJR.09.3940
Cryptogenic Organizing Pneumonia: Serial High-Resolution CT Findings in 22 Patients
resolves10.1097/00004728-200303000-00027
Organizing Pneumonia: Prognostic Implication of High-resolution Computed Tomography Features
resolves10.2214/ajr.154.5.2108572
Bronchiolitis obliterans organizing pneumonia: CT features in 14 patients.
resolves10.2214/ajr.180.5.1801251
<b>Reversed Halo Sign on High-Resolution CT of Cryptogenic Organizing Pneumonia:</b> Diagnostic Implications
resolves10.1016/j.rmed.2009.05.001
Anti-synthetase syndrome in ANA and anti-Jo-1 negative patients presenting with idiopathic interstitial pneumonia
resolves10.1097/00005792-200011000-00003
Acute Interstitial Pneumonitis: Case Series and Review of the Literature
resolves10.1164/rccm.2106157
Acute Interstitial Pneumonia: Comparison of High-Resolution Computed Tomography Findings between Survivors and Nonsurvivors
resolves10.1148/radiology.188.3.8351354
Acute interstitial pneumonia: radiographic and CT findings in nine patients.
resolves10.1148/radiology.211.3.r99jn04859
Acute Interstitial Pneumonia: Thin-Section CT Findings in 36 Patients
resolves10.1148/radiology.210.1.r99ja2629
Acute Respiratory Distress Syndrome: CT Abnormalities at Long-term Follow-up
resolves10.1148/radiol.2373041515
Prediction of Prognosis for Acute Respiratory Distress Syndrome with Thin-Section CT: Validation in 44 Cases
resolves10.1111/j.1440-1843.2008.01277.x
Clinically occult subpleural fibrosis and acute interstitial pneumonia a precursor to idiopathic pulmonary fibrosis?
resolves10.1309/UVARMDY8FE9FJDKU
Terminal Diffuse Alveolar Damage in Relation to Interstitial Pneumonias
resolves10.1183/09031936.00159709
Acute exacerbation of idiopathic pulmonary fibrosis: incidence, risk factors and outcome
resolves10.1016/j.ejim.2007.04.024
Acute exacerbation of idiopathic pulmonary fibrosis: A systematic review
resolves10.1097/01.pas.0000213341.70852.9d
Acute Exacerbation (Acute Lung Injury of Unknown Cause) in UIP and Other Forms of Fibrotic Interstitial Pneumonias
resolves10.1016/j.rmed.2008.12.019
Acute exacerbation of interstitial pneumonia associated with collagen vascular diseases
resolves10.1378/chest.07-0323
Acute Exacerbation of Interstitial Pneumonia Other Than Idiopathic Pulmonary Fibrosis
resolves10.1378/chest.08-0866
Clinical Predictors and Histologic Appearance of Acute Exacerbations in Chronic Hypersensitivity Pneumonitis
resolves10.1164/rccm.200709-1365OC
Computed Tomography Findings in Acute Exacerbation of Idiopathic Pulmonary Fibrosis
resolves10.2214/ajr.168.1.8976924
CT findings during phase of accelerated deterioration in patients with idiopathic pulmonary fibrosis.
resolves10.1007/s00330-011-2211-6
Acute exacerbation of idiopathic pulmonary fibrosis: high-resolution CT scores predict mortality
resolves10.1183/09031936.06.00076705
Lymphoid interstitial pneumonia: clinical features, associations and prognosis
resolves10.1148/radiology.212.2.r99au05567
Lymphocytic Interstitial Pneumonia: Thin-Section CT Findings in 22 Patients
resolves10.1183/09031936.00165111
Pleuroparenchymal fibroelastosis: a spectrum of histopathological and imaging phenotypes
resolves10.1038/modpathol.2008.56
Idiopathic pleuroparenchymal fibroelastosis: an unrecognized or misdiagnosed entity?
resolves10.1038/modpathol.2011.114
Pleuroparenchymal fibroelastosis in patients with pulmonary disease secondary to bone marrow transplantation
resolves10.1016/j.resinv.2012.06.003
Rapid decrease in forced vital capacity in patients with idiopathic pulmonary upper lobe fibrosis
resolves10.1016/j.humpath.2011.06.001
Distinct histopathology of acute onset or abrupt exacerbation of hypersensitivity pneumonitis
resolves10.1097/QAD.0b013e3282f08c5a
Acute fibrinous and organizing pneumonia as a rare presentation of abacavir hypersensitivity reaction
resolves10.1097/01.pas.0000168177.71405.ac
Peribronchiolar Metaplasia: A Common Histologic Lesion in Diffuse Lung Disease and a Rare Cause of Interstitial Lung Disease
resolves10.1016/j.anndiagpath.2007.07.002
Bronchiolitis interstitial pneumonitis: a pathologic study of 31 lung biopsies with features intermediate between bronchiolitis obliterans organizing pneumonia and usual interstitial pneumonitis, with clinical correlation
resolves10.1183/09031936.00131912
Prevalence and prognosis of unclassifiable interstitial lung disease
resolves10.1378/chest.08-2209
Serum Surfactant Protein-A Is a Strong Predictor of Early Mortality in Idiopathic Pulmonary Fibrosis
resolves10.1111/j.1365-2796.2006.01704.x
Increased levels of KL‐6 and subsequent mortality in patients with interstitial lung diseases
resolves10.1164/rccm.200808-1201OC
Serum CC-Chemokine Ligand 18 Concentration Predicts Outcome in Idiopathic Pulmonary Fibrosis
resolves10.1002/art.22559
CCL18 as an indicator of pulmonary fibrotic activity in idiopathic interstitial pneumonias and systemic sclerosis
resolves10.1136/thorax.58.1.52
High serum concentrations of surfactant protein A in usual interstitial pneumonia compared with non-specific interstitial pneumonia
resolves10.1164/ajrccm.165.3.2107134
Comparative Study of KL-6, Surfactant Protein-A, Surfactant Protein-D, and Monocyte Chemoattractant Protein-1 as Serum Markers for Interstitial Lung Diseases
resolves10.5301/JBM.2010.6115
Increased Levels of Free Circulating Dna in Patients with Idiopathic Pulmonary Fibrosis
resolves10.1164/rccm.200502-244OC
Role of the Chemokine Receptors CXCR3 and CCR4 in Human Pulmonary Fibrosis
resolves10.1159/000083399
Increased Levels of Interleukin-18 in Bronchoalveolar Lavage Fluid of Patients with Idiopathic Nonspecific Interstitial Pneumonia
resolves10.1136/jcp.2005.026872
Focal interstitial CC chemokine receptor 7 (CCR7) expression in idiopathic interstitial pneumonia
resolves10.1164/rccm.200401-002OC
Enhanced Monocyte Chemoattractant Protein-3/CC Chemokine Ligand-7 in Usual Interstitial Pneumonia
resolves10.1164/rccm.200601-062OC
Gene Expression Profiling of Familial and Sporadic Interstitial Pneumonia
resolves10.1136/thx.2004.026336
Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF
resolves10.1007/BF03402107
A Plasminogen Activator Inhibitor-1 Promoter Polymorphism and Idiopathic Interstitial Pneumonia
resolves10.1183/09031936.00034406
Surfactant protein C mutations in sporadic forms of idiopathic interstitial pneumonias
resolves10.1164/ajrccm.165.2.2106004
Interleukin-1 Gene Cluster Polymorphisms in Sarcoidosis and Idiopathic Pulmonary Fibrosis
resolves10.1002/1529-0131(200007)43:7<1633::AID-ANR29>3.0.CO;2-9
Distribution of novel polymorphisms of the interleukin-8 and CXC receptor 1 and 2 genes in systemic sclerosis and cryptogenic fibrosing alveolitis
resolves10.1164/rccm.200302-221OC
Complement Receptor 1 Gene Polymorphisms Are Associated with Idiopathic Pulmonary Fibrosis
resolves10.1016/j.rmed.2004.08.003
The polymorphism C5507G of complement receptor 1 does not explain idiopathic pulmonary fibrosis among the Finns
resolves10.1111/j.1399-0039.2008.01133.x
The CR1 C5507G polymorphism is not involved in susceptibility to idiopathic pulmonary fibrosis in two European populations
resolves10.1136/jmg.2008.057356
A genome-wide association study identifies an association of a common variant in <i>TERT</i> with susceptibility to idiopathic pulmonary fibrosis
resolves10.1007/s00439-003-1015-4
Surfactant protein�A and B genetic variants predispose to idiopathic pulmonary fibrosis
resolves10.1007/s00439-005-0035-7
Major histocompatibility complex and alveolar epithelial apoptosis in idiopathic pulmonary fibrosis
resolves10.1164/ajrccm.162.3.9910080
Serum Surfactant Proteins A and D as Prognostic Factors in Idiopathic Pulmonary Fibrosis and Their Relationship to Disease Extent
resolves10.1183/09031936.02.00081102
Serum surfactant proteins‐A and ‐D as biomarkers in idiopathic pulmonary fibrosis
resolves10.1111/j.1440-1843.2006.00834.x
Prognostic value of circulating KL‐6 in idiopathic pulmonary fibrosis
resolves10.1111/j.1440-1843.2006.00809.x
Monitoring markers of disease activity for interstitial lung diseases with serum surfactant proteins A and D
resolves10.1016/j.pupt.2006.10.005
Serum levels of oxidative stress as a marker of disease severity in idiopathic pulmonary fibrosis
resolves10.1371/journal.pmed.0050093
MMP1 and MMP7 as Potential Peripheral Blood Biomarkers in Idiopathic Pulmonary Fibrosis
resolves10.1371/journal.pone.0008959
CD28 Down-Regulation on Circulating CD4 T-Cells Is Associated with Poor Prognoses of Patients with Idiopathic Pulmonary Fibrosis
resolves10.1164/rccm.201101-0058OC
Peripheral Blood Proteins Predict Mortality in Idiopathic Pulmonary Fibrosis
resolves10.1183/09031936.00060708
MMP expression and abnormal lung permeability are important determinants of outcome in IPF
resolves10.1159/000207617
Elevated CC Chemokine Level in Bronchoalveolar Lavage Fluid Is Predictive of a Poor Outcome of Idiopathic Pulmonary Fibrosis
resolves10.1136/thx.2008.102814
Soluble endostatin is a novel inhibitor of epithelial repair in idiopathic pulmonary fibrosis
The 7 references without a DOI — listed, not checked
no DOI — not checkedSurfactant protein-D predicts survival in patients with idiopathic pulmonary fibrosis
no DOI — not checkedThe definition of emphysema: report of a National Heart, Lung, and Blood Institute, Division of Lung Diseases workshop
no DOI — not checkedCryptogenic organizing pneumonia: clinical profile in a series of 34 admitted patients in a hospital in India
no DOI — not checkedIdiopathic pulmonary upper lobe fibrosis (IPUF) [in Japanese]
no DOI — not checkedAcute fibrinous and organizing pneumonia in a patient with collagen vascular disease “stigma.”
no DOI — not checkedNOD2/CARD15 gene polymorphisms in idiopathic pulmonary fibrosis
no DOI — not checkedPathologic findings both before and after steroid therapy in a case of desquamative interstitial pneumonia [article in Japanese]
What this badge says. CiteStamped means the CHECKABLE references of this
work were clean at the dated check: each resolved to a known work in a public registry, and none
carried a retraction notice at that time. It says nothing about the quality, findings,
or importance of the work itself, and nothing about references deposited without a DOI.
checked 2026-07-25 — re-checked daily as this page is visited; titles and statuses come from Crossref and DataCite and are not part of the signed record
Embed this badge
Both snippets point at the live badge image and link back to this page. The badge re-renders from the daily check, so an embed never goes stale by more than a day of visits.
<a href="https://citestamp.com/citestamped/10.1164/rccm.201308-1483st"><img src="https://citestamp.com/citestamped/10.1164/rccm.201308-1483st/badge.svg" alt="CiteStamped reference-health badge" width="460" height="64"></a>
[](https://citestamp.com/citestamped/10.1164/rccm.201308-1483st)