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pmid: 1208551
Scleroderma is a disease of mesenchymal tissues characterized by fibrosis and vascular changes which eventually lead to organ insufficiency. Two clinical forms have been recognized, localized and systemic scleroderma. The localized form only affects the skin and the lesions have a tendency to resolve spontaneously. Systemic scleroderma is a progressive, usually irreversible process and the organs most frequently involved are the skin, gastrointestinal tract, lungs and kidneys. The following findings strongly suggest that involvement of small blood vessels (capillaries, arterioles and small size arteries) plays an important role in the pathogenesis of systemic scleroderma: (a) the frequent presence of Raynaud's phenomenon, (b) marked reduction in the number of dermal capillaries, (c) increase in thickness of the basement membrane of muscle capillaries (16), (d) thickening and hyalinization of arterioles (e) intimal proliferation of small size arteries, and (f) eventual ischemic necrosis (2, 3, 17). Small b...
Adult, Male, Scleroderma, Systemic, Adolescent, Biopsy, Middle Aged, Scleroderma, Localized, Hypertension, Renin, Humans, Female, Child, Aged, Skin
Adult, Male, Scleroderma, Systemic, Adolescent, Biopsy, Middle Aged, Scleroderma, Localized, Hypertension, Renin, Humans, Female, Child, Aged, Skin
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 26 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |