Results 221 to 230 of about 56,738 (264)
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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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Rheumatic Disease Clinics of North America, 2003
The pathogenesis of fibrosis in scleroderma involves a complex set of interactions between the fibroblast and its surroundings. Multiple fibrotic pathways are activated for reasons that are not completely clear, but involve immune activation, microvascular damage, and fibroblast transformation into the myofibroblast.
Eugene Y, Kissin, Joseph H, Korn
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The pathogenesis of fibrosis in scleroderma involves a complex set of interactions between the fibroblast and its surroundings. Multiple fibrotic pathways are activated for reasons that are not completely clear, but involve immune activation, microvascular damage, and fibroblast transformation into the myofibroblast.
Eugene Y, Kissin, Joseph H, Korn
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Seminars in Cutaneous Medicine and Surgery, 1998
Scleroderma is a diverse group of conditions which have in common fibrosis of skin and other tissues. Although less common in children than in adults, these conditions are an important cause of morbidity and occasional mortality when they occur in the pediatric population.
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Scleroderma is a diverse group of conditions which have in common fibrosis of skin and other tissues. Although less common in children than in adults, these conditions are an important cause of morbidity and occasional mortality when they occur in the pediatric population.
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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
Yoshihide, Asano, Shinichi, Sato
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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
Yoshihide, Asano, Shinichi, Sato
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Scleroderma and Pseudo-Scleroderma.
Archives of Internal Medicine, 1968This book appeared in Poland in 1963 and was translated for the National Library of Medicine in 1965. It is unlike most American textbooks, particularly as it takes an editorial stance and evaluates data from this perspective. The author favors the neurogenic theory, which is at variance with most American opinions.
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The Journal of Pediatrics, 1974
Twelve children with scleroderma are presented. All had characteristic cutaneous abnormalities and manifestations of visceral involvement. Raynaud's phenomenon and joint symptoms frequently prompted medical consultation. The presence of visceral disease may be overlooked unless specific diagnostic procedures such as pulmonary function testing ...
L, Dabich, D B, Sullivan, J T, Cassidy
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Twelve children with scleroderma are presented. All had characteristic cutaneous abnormalities and manifestations of visceral involvement. Raynaud's phenomenon and joint symptoms frequently prompted medical consultation. The presence of visceral disease may be overlooked unless specific diagnostic procedures such as pulmonary function testing ...
L, Dabich, D B, Sullivan, J T, Cassidy
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Seminars in Cutaneous Medicine and Surgery, 1998
Localized scleroderma can be divided into three main subtypes: morphea, linear scleroderma, and generalized morphea. Plaque morphea usually has a good prognosis. Variants of morphea, including guttate morphea and atrophoderma of Pasini and Pierini, are seen.
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Localized scleroderma can be divided into three main subtypes: morphea, linear scleroderma, and generalized morphea. Plaque morphea usually has a good prognosis. Variants of morphea, including guttate morphea and atrophoderma of Pasini and Pierini, are seen.
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Rheumatic Disease Clinics of North America, 2007
Pregnancy in systemic sclerosis may be uneventful with good maternal and fetal outcomes. Scleroderma is a multisystem disease and complications do occur; however, careful antenatal evaluations, discussion of potential problems, and participation in a high-risk obstetric monitoring program are important to optimize the best outcome.
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Pregnancy in systemic sclerosis may be uneventful with good maternal and fetal outcomes. Scleroderma is a multisystem disease and complications do occur; however, careful antenatal evaluations, discussion of potential problems, and participation in a high-risk obstetric monitoring program are important to optimize the best outcome.
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Microchimerism and scleroderma
Current Rheumatology Reports, 1999It is now known that cells traffic between fetus and mother during normal human pregnancy. Moreover, fetal cells have been found to persist in the maternal peripheral blood for decades after childbirth. Chronic graft-versus-host disease, a known condition of chimerism that occurs after allogeneic hematopoietic stem cell transplantation has clinical ...
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