Results 221 to 230 of about 39,459 (248)
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Genetic and immunological differences between Japanese patients with diffuse scleroderma and limited scleroderma.

The Journal of rheumatology, 1994
To study the association between HLA-DR and scleroderma (SSc), subsets of SSc, and autoantibodies in SSc.HLA-DR antigens were determined in 45 Japanese patients with SSc. The association between HLA-DR and SSc, subsets of SSc, and autoantibodies was analyzed in 22 patients with SSc excluding mixed connective tissue disease (MCTD)/overlap syndrome (OL ...
M, Satoh   +8 more
openaire   +1 more source

Pulmonary hypertension with limited cutaneous scleroderma (CREST syndrome).

The Netherlands journal of medicine, 2001
A patient is described with a typical manifestation of pulmonary hypertension associated with limited cutaneous scleroderma, also known as CREST syndrome. The patient was treated with a calcium antagonist, oral anticoagulation and, because of evidence for parenchymal inflammation of the lung, with low-dose prednisone and cyclophosphamide.
J C, Berends   +3 more
openaire   +1 more source

Calcinosis Cutis as the Initial Manifestation of Limited Scleroderma

JCR: Journal of Clinical Rheumatology, 2020
Shannon, Zalewski   +2 more
openaire   +2 more sources

Diffuse Blisters and Erosions in a Patient With Limited Scleroderma

Archives of Dermatology, 1997
REPORT OF A CASE A 65-year-old white woman with a 2-year history of limited scleroderma with interstitial lung disease was sent by the rheumatology clinic for the evaluation of increasing numbers of pruritic blistering lesions that had been forming on her face, neck, and trunk for 3 weeks. These lesions ruptured within hours after formation.
openaire   +1 more source

[Finger tip necroses after dihydroergotamine medication in limited systemic scleroderma].

Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1999
A 78 year old women developed acute fingertip necrosis just a few days after starting dihydroergotamine. The lesions healed in 3 weeks after the medication was stopped. The patient had suffered from Raynaud syndrome for 5 years and limited systemic sclerosis was diagnosed during the necrotic episode.
T, Hahne, B R, Balda
openaire   +1 more source

A Rare Case of Lymphocytic Interstitial Pneumonia in Limited Scleroderma

B33. CASE REPORTS: IMMUNE CELLS GONE HAYWIRE, 2022
A. Dursun, B. Giri
openaire   +1 more source

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