Hamman-Rich syndrome

Known as: Fibrosing Alveolitides, usual interstitial pneumonia, Fibrosing Alveolitis 
 

Topic mentions per year

Topic mentions per year

1951-2018
020406019512017

Papers overview

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Highly Cited
2008
Highly Cited
2008
RATIONALE Patients with a clinicopathological diagnosis of idiopathic pulmonary fibrosis (IPF) may have typical findings of usual… (More)
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Highly Cited
2004
Highly Cited
2004
To elucidate the apparent contradictions in vascular remodeling in the lungs of patients with idiopathic pulmonary fibrosis, we… (More)
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Highly Cited
2003
Highly Cited
2003
Exercise-induced hypoxia is an index of the severity of interstitial lung disease. We hypothesized that desaturation during a 6… (More)
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Highly Cited
2003
Highly Cited
2003
Idiopathic interstitial pneumonias are a diverse group of lung diseases with varied prognoses. We hypothesized that changes in… (More)
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Highly Cited
2003
Highly Cited
2003
The aim of this study was to evaluate interstitial vascularity in cryptogenic fibrosing alveolitis (CFA) and in fibrosing… (More)
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Highly Cited
2002
Highly Cited
2002
Familial pulmonary fibrosis is a heterogeneous group of interstitial lung diseases of unknown cause that is associated with… (More)
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Highly Cited
2001
Highly Cited
2001
Usual interstitial pneumonia (UIP) is a specific histological pattern of interstitial pneumonia most often associated with the… (More)
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Highly Cited
2000
Highly Cited
2000
Nonspecific interstitial pneumonia (NSIP) has been proposed as a histologic subtype of idiopathic interstitial pneumonia with… (More)
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Highly Cited
1998
Highly Cited
1998
Epidemiological studies indicate that the use of aspirin decreases incidence of and mortality from gastrointestinal cancers. A… (More)
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Highly Cited
1997
Highly Cited
1997
In fibrosing alveolitis (FA), activated phagocytes cause excessive oxidative stress in the lower respiratory tract. Additionally… (More)
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