Results 251 to 260 of about 80,483 (293)
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American Journal of Obstetrics and Gynecology, 1968
Abstract Scleroderma, classified as a collagen disease, usually becomes clinically apparent during the fourth and fifth decades of life. Pregnancy together with scleroderma is seldom observed. Seven of 66 female patients with scleroderma admitted to the Los Angeles County General Hospital during a 13½ year period had concomitant scleroderma and ...
A.Richard Graham, William G. Slate
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Abstract Scleroderma, classified as a collagen disease, usually becomes clinically apparent during the fourth and fifth decades of life. Pregnancy together with scleroderma is seldom observed. Seven of 66 female patients with scleroderma admitted to the Los Angeles County General Hospital during a 13½ year period had concomitant scleroderma and ...
A.Richard Graham, William G. Slate
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Seminars in Immunopathology, 2015
Systemic sclerosis (SSc) is a multisystem connective tissue disorder featured by vascular injury and fibrosis of the skin and various internal organs with autoimmune background. Although the pathogenesis of SSc still remains elusive, it is generally accepted that initial vascular injury due to autoimmunity and/or environmental factors causes structural
Shinichi Sato, Yoshihide Asano
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Systemic sclerosis (SSc) is a multisystem connective tissue disorder featured by vascular injury and fibrosis of the skin and various internal organs with autoimmune background. Although the pathogenesis of SSc still remains elusive, it is generally accepted that initial vascular injury due to autoimmunity and/or environmental factors causes structural
Shinichi Sato, Yoshihide Asano
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Melorheostosis with scleroderma
Clinical Imaging, 2004The association of linear scleroderma with melorheostosis is very rare. Until now, only a few cases have been reported in the English literature. We describe a case of melorheostosis of a rib associated with overlying skin changes.
Gamanagatti Shivanand +1 more
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Journal of the American Academy of Dermatology, 1987
After a review of some pathogenetic and pathologic aspects of scleroderma, the experimental effects of a group of agents that can inhibit the formation of connective tissue, especially the biosynthesis of collagen, are mentioned. These substances were transferred to clinical therapy of scleroderma.
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After a review of some pathogenetic and pathologic aspects of scleroderma, the experimental effects of a group of agents that can inhibit the formation of connective tissue, especially the biosynthesis of collagen, are mentioned. These substances were transferred to clinical therapy of scleroderma.
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2008
The prototypic autoimmune diseases involving skin (lupus, dermatomyositis) typically result in epithelial injury and autoantibodies to characteristic cellular antigens. Disease-specific autoantibodies are also found in scleroderma, but scleroderma is different from other cutaneous autoimmune diseases because epithelial injury does not occur.
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The prototypic autoimmune diseases involving skin (lupus, dermatomyositis) typically result in epithelial injury and autoantibodies to characteristic cellular antigens. Disease-specific autoantibodies are also found in scleroderma, but scleroderma is different from other cutaneous autoimmune diseases because epithelial injury does not occur.
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Best Practice & Research Clinical Rheumatology, 2005
Juvenile scleroderma with its two varieties, juvenile localized scleroderma and systemic sclerosis (SSc), represents the third most frequent rheumatic disease in childhood. In juvenile SSc, new developments have been recently reported in the fields of classification and monitoring.
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Juvenile scleroderma with its two varieties, juvenile localized scleroderma and systemic sclerosis (SSc), represents the third most frequent rheumatic disease in childhood. In juvenile SSc, new developments have been recently reported in the fields of classification and monitoring.
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Obstetrical & Gynecological Survey, 1989
We conducted a detailed literature search for the rare combination of scleroderma and pregnancy. Ninety-four patients were reported, 14 of whom died during the course of the pregnancy, mainly due to secondary renal and cardiopulmonary involvement. Out of the 95 fetuses, 19 were lost.
Moshe Fejgin, Ron Maymon
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We conducted a detailed literature search for the rare combination of scleroderma and pregnancy. Ninety-four patients were reported, 14 of whom died during the course of the pregnancy, mainly due to secondary renal and cardiopulmonary involvement. Out of the 95 fetuses, 19 were lost.
Moshe Fejgin, Ron Maymon
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Rheumatic Disease Clinics of North America, 1996
Evidence from multiple sources indicates that SSc does not occur randomly in the population; there are particular groups who are at greater risk. The overall incidence rate of SSc in the adult population of the United States is approximately 20 per million per year; this rate has increased from 1944 to 1973, but has been relatively stable since that ...
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Evidence from multiple sources indicates that SSc does not occur randomly in the population; there are particular groups who are at greater risk. The overall incidence rate of SSc in the adult population of the United States is approximately 20 per million per year; this rate has increased from 1944 to 1973, but has been relatively stable since that ...
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Current Opinion in Rheumatology, 2006
Localized scleroderma, also known as morphoea, has a variety of clinical manifestations that can include systemic involvement. Early recognition, diagnosis and treatment may improve the long-term outcome.A large multicentre study coordinated by the Pediatric Rheumatology European Society has yielded important information on the epidemiology and ...
Francesco Zulian, Ronald M. Laxer
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Localized scleroderma, also known as morphoea, has a variety of clinical manifestations that can include systemic involvement. Early recognition, diagnosis and treatment may improve the long-term outcome.A large multicentre study coordinated by the Pediatric Rheumatology European Society has yielded important information on the epidemiology and ...
Francesco Zulian, Ronald M. Laxer
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Annals of Internal Medicine, 1953
Excerpt When the etiology of a disease is unknown its treatment is at best haphazard. This has heretofore been the fate of Raynaud's disease and scleroderma.
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Excerpt When the etiology of a disease is unknown its treatment is at best haphazard. This has heretofore been the fate of Raynaud's disease and scleroderma.
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