Results 201 to 210 of about 41,669 (215)
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Systemic manifestations in localized scleroderma
Current Rheumatology Reports, 2004In this paper, the various systemic manifestations reported in localized scleroderma, their incidence, their relationship with systemic sclerosis, and their relationship with other autoimmune or connective tissue diseases will be analyzed.
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1999
Abstract The next two chapters will deal with the systemic forms of scleroderma, both diffuse and, as well as scleroderma sine sclerosis, in which there is internal organ involvement but no thickening of the skin (sine means without and sclerosis means hardening). The term systemic means that this form of scleroderma affects the internal
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Abstract The next two chapters will deal with the systemic forms of scleroderma, both diffuse and, as well as scleroderma sine sclerosis, in which there is internal organ involvement but no thickening of the skin (sine means without and sclerosis means hardening). The term systemic means that this form of scleroderma affects the internal
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Systemic and localized scleroderma in children
Current Opinion in Rheumatology, 1996All forms of scleroderma are rare in childhood. The most common form in childhood is localized scleroderma, which may take the form of morphea or linear scleroderma. Localized scleroderma is often benign but may cause significant deformity if it occurs on the face or extends across joint surfaces. Progressive systemic sclerosis is much less frequent in
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1999
Abstract We left our patient with limited scleroderma in chapter 3 at the point of being diagnosed. Let us pick up the story there and continue with the scenario. As you recall, she developed Raynaud’s phenomenon (color changes of the fingers on cold exposure) in 1999, puffy fingers and chronic heartburn in 2001, and a fingertip sore in ...
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Abstract We left our patient with limited scleroderma in chapter 3 at the point of being diagnosed. Let us pick up the story there and continue with the scenario. As you recall, she developed Raynaud’s phenomenon (color changes of the fingers on cold exposure) in 1999, puffy fingers and chronic heartburn in 2001, and a fingertip sore in ...
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Systemic Sclerosis (Scleroderma)
2019Systemic sclerosis (SSc) is a rare systemic chronic disease characterized by widespread fibrosis of skin and internal organs, microvasculopathy, and autoantibodies that frequently affects internal organs and quality of life and survival. Disease-related autoantibodies, anti-topoisomerase I, anticentromere, and anti-RNA polymerase III antibodies ...
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Infantile systemic scleroderma.
Archives of dermatology, 1967R Fleischmajer, R Koelsch
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Photochemotherapy for systemic and localized scleroderma
Journal of the American Academy of Dermatology, 2000Jan D. Bos, Menno A. de Rie
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