Results 321 to 330 of about 542,433 (374)

Central retinal artery occlusion as the initial manifestation of mixed connective tissue disease in a young woman: a case report. [PDF]

BMC Ophthalmol
Liu K, Liu Y, Yang X, Cui L, Chen C.
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Lung imaging patterns in connective tissue disease-associated interstitial lung disease impact prognosis and immunosuppression response. [PDF]

Rheumatology (Oxford)
Zheng B, Marinescu DC, Hague CJ, Muller NL, Murphy D, Churg A, Wright JL, Al-Arnawoot A, Bilawich AM, Bourgouin P, Cox G, Durand C, Elliot T, Ellis J, Fisher JH, Fladeland D, Grant-Orser A, Goobie GC, Guenther Z, Haider E, Hambly N, Huynh J, Johannson KA, Karjala G, Khalil N, Kolb M, Leipsic J, Lok SD, MacIsaac S, McInnis M, Manganas H, Marcoux V, Mayo J, Morisset J, Scallan C, Sedlic T, Shapera S, Sun K, Tan V, Wong AW, Ryerson CJ.   +40 more
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Rituximab therapy in severe connective tissue disease associated interstitial lung disease: A retrospective single-centre observational study. [PDF]

Afr J Thorac Crit Care Med
Seedat UF, Christian B, Boshoff PE, Gaylard P, Schleicher GK.   +4 more
europepmc   +1 more source

Immunological characteristics of bronchoalveolar lavage fluid and blood across connective tissue disease-associated interstitial lung diseases. [PDF]

Front Immunol
Hirano A, Sakashita A, Fujii W, Baßler K, Tsuji T, Kadoya M, Omoto A, Hiraoka N, Imabayashi T, Kaneko Y, Sofue H, Maehara Y, Seno T, Wada M, Kohno M, Fukuda W, Yamada K, Takayama K, Kawahito Y.   +18 more
europepmc   +1 more source

Connective Tissue Diseases [PDF]

Plastic and Reconstructive Surgery, 1985
The connective tissue disorders are a group of systemic rheumatic diseases characterized by a propensity for multisystem involvement early in the course of the disease, and arthropathies which tend to be mild, non-erosive and in general non-deforming.
Nicholas Bellamy, Nicholas Bellamy
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Connective Tissue Diseases

Clinics in Plastic Surgery, 1993
The classic connective tissue diseases (lupus erythematosus, dermatomyositis, and scleroderma) have been described with respect to their pathogenesis, clinical picture, laboratory diagnosis, and management. Because the aim of this volume is to provide an interface between plastic surgery and dermatology, the cutaneous manifestations, both shared and ...
Maria L.C. Turner, Maria L.C. Turner
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Mixed Connective Tissue Disease

Archives of Internal Medicine, 1976
Three patients with mixed connective tissue disease (MCTD) had clinical features that included a high incidence of Raynaud phenomenon, arthritis, myositis, and swollen hands. The diagnostic laboratory test result was the presence of high titers of antibody to extractable nuclear antigen.
Wilfred Minkin, Nathan B. Rabhan
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Mixed Connective Tissue Disease

Current Opinion in Rheumatology, 2000
A defining feature of mixed connective tissue disease (MCTD) is the presence of antibodies against the U1-ribonucleoprotein (RNP) complex, but other autoantibodies in MCTD have recently been described. Research has also further elucidated the immune responses directed against U1-RNP in humans and in murine models of disease.
Eric L. Greidinger, Robert W. Hoffman
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Connective tissue disease and silicosis

American Journal of Industrial Medicine, 1999
To determine the prevalence of connective tissue disease in a cohort of individuals with silicosis, we reviewed the medical records and questionnaires from individuals reported from 1987 to 1995 to a state surveillance system for silicosis. Reporting of individuals with silicosis is required by state law.
Kenneth D. Rosenman, Mark Moore-Fuller, Mary Jo Reilly   +2 more
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