Results 241 to 250 of about 80,483 (293)
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New England Journal of Medicine, 2009
Scleroderma (systemic sclerosis) is a complex disease in which extensive fibrosis, vascular alterations, and autoantibodies against various cellular antigens are among the principal features There are two major subgroups in the commonly accepted classification of scleroderma: limited cutaneous scleroderma and diffuse cutaneous scleroderma.
Gabrielli A.+2 more
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Scleroderma (systemic sclerosis) is a complex disease in which extensive fibrosis, vascular alterations, and autoantibodies against various cellular antigens are among the principal features There are two major subgroups in the commonly accepted classification of scleroderma: limited cutaneous scleroderma and diffuse cutaneous scleroderma.
Gabrielli A.+2 more
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Gastroenterology Clinics of North America, 2021
The gastrointestinal tract is the second largest organ system in the body and is often affected by connective tissue disorders. Scleroderma is the classic rheumatologic disease affecting the esophagus; more than 90% of patients with scleroderma have esophageal involvement.
Nitin K. Ahuja, John O. Clarke
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The gastrointestinal tract is the second largest organ system in the body and is often affected by connective tissue disorders. Scleroderma is the classic rheumatologic disease affecting the esophagus; more than 90% of patients with scleroderma have esophageal involvement.
Nitin K. Ahuja, John O. Clarke
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Best Practice & Research Clinical Rheumatology, 1995
In practice, the classification of scleroderma is less problematic than that of most other connective tissue diseases given the distinctive pattern of skin involvement. Classification of early and limited disease is more problematic and is difficult to separate from severe forms of Raynaud's phenomenon. Division of scleroderma into two groups depending
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In practice, the classification of scleroderma is less problematic than that of most other connective tissue diseases given the distinctive pattern of skin involvement. Classification of early and limited disease is more problematic and is difficult to separate from severe forms of Raynaud's phenomenon. Division of scleroderma into two groups depending
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Rheumatic Disease Clinics of North America, 1989
This article reviews the literature on scleroderma and pregnancy, highlighting its sparsity, confused state, and retrospective nature. It emphasizes the need for more informed prospective work. This is required for clinical management and to help understand the complex interaction between scleroderma and pregnancy.
C M, Black, W M, Stevens
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This article reviews the literature on scleroderma and pregnancy, highlighting its sparsity, confused state, and retrospective nature. It emphasizes the need for more informed prospective work. This is required for clinical management and to help understand the complex interaction between scleroderma and pregnancy.
C M, Black, W M, Stevens
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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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Annals of Internal Medicine, 1985
Excerpt To the editor: Schneider and colleagues (1) have emphasized that esophageal motor abnormalities commonly found in patients with scleroderma are nonspecific.
BASSOTTI, GABRIO+3 more
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Excerpt To the editor: Schneider and colleagues (1) have emphasized that esophageal motor abnormalities commonly found in patients with scleroderma are nonspecific.
BASSOTTI, GABRIO+3 more
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2004
Abstract Scleroderma is a broad term that simply means “hard skin.” A variety of different diseases are grouped together under this diagnosis. The focal (or localized) forms of scleroderma are often mild and may not require any treatment.
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Abstract Scleroderma is a broad term that simply means “hard skin.” A variety of different diseases are grouped together under this diagnosis. The focal (or localized) forms of scleroderma are often mild and may not require any treatment.
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