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Werner’s syndrome: a quite rare disease for differential diagnosis of scleroderma
Rheumatology International, 06/16/09
Bes C et al. - Werner’s syndrome (WS) is an autosomal recessive disorder characterized by premature aging. The main features of the disease are scleroderma-like skin appearance, premature atherosclerosis, short stature, diabetes mellitus, early osteoporosis and early aging. Herein, the authors describe a patient with WS, who has scleroderma-like skin changes and discuss the literature about WS as a disease in the differential diagnosis of systemic sclerosis.
Today in Autoimmune/Heritable...keeping you current
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Clinical and histologic evidence of salivary gland restoration supports the efficacy of rituximab treatment in Sjögrens syndrome
Arthritis & Rheumatism, 11/06/09
A prospective open-label study of mycophenolate mofetil for the treatment of diffuse systemic sclerosis
Rheumatology, 10/23/09
Vaccination, atherosclerosis and systemic lupus erythematosus
Lupus, 11/05/09
Today in Connective Tissue Dz...keeping you current
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Nephrogenic systemic fibrosis
Current Opinion in Rheumatology, 11/04/09
Effect of Sildenafil on digital ulcers in systemic sclerosis - analysis from a single centre pilot study
Annals of Rheumatic Diseases, 11/23/09
Comparison of injection methods in myofascial pain syndrome: A randomized controlled trial
Clinical Rheumatology, 10/27/09
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