Pharmacological implications in the switch from acute to chronic inflammation

Author:

Dallegri Franco,Ottonello Luciano

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology,Immunology

Reference24 articles.

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2. Baracchini, A., Minisola, G., Amicosante, G., et al. (2001). Oxaprozin: a NSAID able to inhibit the matrix metallo-proteinase activity, Inflammopharmacology 9, 143–146.

3. Bevilacqua, M. (2000). Pharmacology of oxaprozin: novel findings, in: Oxaprozin and the daily management of osteomuscolar impairment in arthritic patients, Highlights from the Satellite Symposium on Oxaprozin at the XIV EULAR Congress, pp. 3–6. Adis International, Milan, Italy.

4. Bevilacqua, M. (2002). Oxaprozin, a derivative of 2-arylpropionic acid, inhibits nuclear factor-kB at therapeuticallyrelevant concentrations, Ann. Rheum. Dis. 61 (Suppl. 1), p. 355, Abstract n. 18.

5. Choy, E. H. S. and Panayi, G. S. (2001). Cytokine pathways and joint inflammation in rheumatoid arthritis, New Engl. J. Med. 344, 907–916.

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