Page last updated: 2024-10-31

nafamostat and Scleroderma, Systemic

nafamostat has been researched along with Scleroderma, Systemic in 1 studies

nafamostat: inhibitor of trypsin, plasmin, pancreatic kallikrein, plasma kallikrein & thrombin; strongly inhibits esterolytic activities of C1r & C1 esterase complement-mediated hemolysis; antineoplastic

Scleroderma, Systemic: A chronic multi-system disorder of CONNECTIVE TISSUE. It is characterized by SCLEROSIS in the SKIN, the LUNGS, the HEART, the GASTROINTESTINAL TRACT, the KIDNEYS, and the MUSCULOSKELETAL SYSTEM. Other important features include diseased small BLOOD VESSELS and AUTOANTIBODIES. The disorder is named for its most prominent feature (hard skin), and classified into subsets by the extent of skin thickening: LIMITED SCLERODERMA and DIFFUSE SCLERODERMA.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Wild, G1
Watkins, J1
Ward, AM1
Hughes, P1
Hume, A1
Rowell, NR1

Other Studies

1 other study available for nafamostat and Scleroderma, Systemic

ArticleYear
Complement activation in systemic sclerosis.
    Journal of clinical & laboratory immunology, 1990, Volume: 31, Issue:1

    Topics: Adult; Benzamidines; Complement Activation; Complement C1q; Complement C3; Complement C3a; Complemen

1990