Lymphoid interstitial pneumonia (LIP) presenting as a tumor Source: Eur Respir J 2005; 26: Suppl. 49, 84s Year: 2005
Association between Epstein-Barr virus and lymphoid interstitial pneumonitis in Brazilian HIV-infected children Source: Eur Respir J 2005; 26: Suppl. 49, 166s Year: 2005
Lymphoid interstitial pneumonia: clinical features, associations and prognosis Source: Eur Respir J 2006; 28: 364-369 Year: 2006
Enhanced apoptosis of alveolar lymphocytes (AL), but not macrophages (AM) in interstitial idiopathic pneumonias (IIPs). Special attention to idiopathic pulmonary fibrosis (IPF) results Source: Annual Congress 2010 - Pathogenesis of diffuse parenchymal lung disease Year: 2010
CD8 BAL lymphocytosis differentiates usual interstitial pneumonia (UIP) from sarcoidosis (SA); correlation with clinical parameters Source: Eur Respir J 2001; 18: Suppl. 33, 195s Year: 2001
The prevalence of neoplastic transformation in idiopathic pulmonary fibrosis (IPF) lungs. A report from a transplanted IPF population Source: Annual Congress 2011 - Genetic and molecular background in pulmonary fibrosis Year: 2011
Elevated apoptosis rate of alveolar lymphocytes (AL) in idiopathic pulmonary fibrosis (IPF) and nonspecific interstitial pneumonitis (NSIP) – strong positive correlation with bronchoalvoelar lavage (BAL) neutrophil count. Source: Virtual Congress 2020 – Translational aspects of idiopathic pulmonary fibrosis Year: 2020
Differences in alveolar cell populations, natural killer cells and lymphocyte subsets between pulmonary sarcoidosis (PS) and idiopathic pulmonary fibrosis (IPF) Source: Eur Respir J 2006; 28: Suppl. 50, 745s Year: 2006
Autopsy-proven causes of diffuse pulmonary infiltrate in patients infected with HIV Source: Eur Respir J 2005; 26: Suppl. 49, 541s Year: 2005
Cytomegalovirus (CMV) damage of the lungs associated with pulmonary tumours: is it a fortuitousness or a rule? Source: Eur Respir J 2003; 22: Suppl. 45, 249s Year: 2003
Activated lymphoid follicles, sign of an immune response, are present in early idiopathic pulmonary fibrosis (IPF) and increase with disease progression. Source: Virtual Congress 2021 – Biomarkers and e-health in idiopathic interstitial pneumonia Year: 2021
Alveolar lymphocytes (AL) apoptosis in interstitial lung diseases (ILD). Increased AL apoptosis rate in idiopathic pulmonary fibrosis (IPF) Source: Annual Congress 2009 - Pathogenesis of pulmonary fibrosis Year: 2009
Massive apoptosis of alveolar lymphocytes (AL) in the course of pulmonary sarcoidosis (PS) as a predictor of disease remission Source: Eur Respir J 2005; 26: Suppl. 49, 80s Year: 2005
Small airways structural alterations in usual interstitial pneumonia (UIP), non-specific interstitial pneumonia (NSIP), hypersensitivity pneumonia (HP) and chronic bronchiolitis (CB) Source: Eur Respir J 2006; 28: Suppl. 50, 308s Year: 2006
Comparative proteome analysis of lung tissue from patients with idiopathic pulmonary fibrosis (IPF) and non-specific interstitial pneumonia (NSIP) Source: Annual Congress 2013 –Connective tissue disease and interstitial lung disease Year: 2013
Isolated mosaic pattern due to bronchiolitis in non-transplant patients: Etiology in 60 cases Source: International Congress 2015 – Interstitial lung diseases I Year: 2015
Cavitary lung masses in SLE patients: an unusual manifestation of CMV infection Source: Eur Respir J 2004; 24: 182-184 Year: 2004
Interstitial pneumonitis in Brazilian HIV-1 infected children: Epstein-Barr virus gene expression and lymphocyte populations Source: Annual Congress 2008 - Pulmonary infections in children - rare but important aspects Year: 2008
A case of lymphoid interstitial pneumonia associated with common variable immunodeficiency Source: Annual Congress 2012 - Diffuse parenchymal lung disease II Year: 2012
Index of histological activity in idiopathic pulmonary fibrosis (IPF) and chronic interstitial lung diseases (CHILD) Source: Eur Respir J 2004; 24: Suppl. 48, 533s Year: 2004