Towards a functional proteomics approach to the comprehension of idiopathic pulmonary fibrosis, sarcoidosis, systemic sclerosis and pulmonary Langerhans cell histiocytosis

Author:

Landi C.,Bargagli E.,Bianchi L.,Gagliardi A.,Carleo A.,Bennett D.,Perari M.G.,Armini A.,Prasse A.,Rottoli P.,Bini L.

Funder

FIRB

Publisher

Elsevier BV

Subject

Biochemistry,Biophysics

Reference56 articles.

1. PET scanning in sarcoidosis;Jain;Ann N Y Acad Sci,2011

2. Idiopathic pulmonary fibrosis: treatment update;O'Connell;Adv Ther,2011

3. Idiopathic pulmonary fibrosis: guidelines for diagnosis and clinical management have advanced from consensus-based in 2000 to evidence-based in 2011;Raghu;Eur Respir J,2011

4. Uncommon features of pulmonary Langerhans' cell histiocytosis: analysis of 11 cases and a review of the literature;Ling;Chin Med J,2010

5. Pulmonary Langerhans cell histiocytosis: emerging concepts in pathobiology, radiology, and clinical evolution of disease;Sundar;Chest,2003

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