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системная склеродермия Portuguese
esclerose sistêmica Spanish
esclerosis sistemica progresiva Catalan
esclerosi sistèmica 
Scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies.
1
In SSc, fibrinolysis system may become a potential target for new therapies.
2
SSCs for P. aeruginosa provide incomplete information regarding the source of infection.
3
Criteria of the American College of Rheumatology were used to diagnose SSc.
4
Our case studies indicate that SSc-RA overlap may be a distinct entity.
5
SSC members have been involved in kidnappings and intimidation across the country.
1
This result would be helpful in cloning the pss1 gene.
2
IL7R expression was decreased in T cells from pSS patients versus controls.
3
This PSS was found to significantly predict the prognosis in group B.
4
The 'quality of life' score showed a high correlation with the I-PSS.
5
PSS with rat blood only induced a small increase in HPV amplitude.
1
Progressive systemic sclerosis (PSS) is characterized in its first phases by vascular damage.
1
Pathologic explanation of the roentgenographically identified diffuse sclerosis in ES has not been previously well documented in the medical literature.
1
A 64-year-old woman with a two-year history of diffuse scleroderma responsible for severe interstitial lung disease was admitted for recurrent loss of consciousness.
1
Background: The impact of systemic sclerosis on bowel function is still unknown.
2
Therefore, further studies of colorectal pathophysiology in patients with systemic sclerosis are needed.
3
Decreased levels of angiotensin converting enzyme plasma activity were found in systemic sclerosis.
4
The natural history of the pulmonary involvement in systemic sclerosis is not well studied.
5
Anorectal manometry cannot differentiate between patients with and without gastrointestinal involvement of systemic sclerosis.
1
We report AZA-induced drug eruption that developed in two cases of systemic scleroderma with polymyositis.
2
One child also had features of systemic scleroderma overlap and one patient had patchy lipoatrophy.