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Behçet syndrome: the vascular cluster.
Turk J Med Sci
November 2016
Department of Rheumatology, Cerrahpaşa Faculty of Medicine, İstanbul University, İstanbul, Turkey.
Although skin-mucosa lesions are common in almost all patients with Behçet syndrome (BS), clinical properties may differ from one patient to another. Within BS, there are subsets with different organ involvement and hence probably different pathological pathways. These subsets can be described as a) solo skin-mucosa disease with no major organ involvement, b) eye disease, c) seronegative spondyloarthropathy-like disease (arthritis, enthesopathy, and folliculitis), d) Crohn-like disease, and finally the topic of this chapter: e) vascular disease.
View Article and Find Full Text PDFSpondyloarthropathy-Like Findings and Diffuse Osteosclerosis as the Presenting Feature of Pseudohypoparathyroidism.
J Clin Rheumatol
March 2016
Department of Rheumatology, King George's Medical University, Lucknow, India Department of Rheumatology, King George's Medical University, Lucknow, India Department of Radiology, King George's Medical University, Lucknow, India Department of Rheumatology, King George's Medical University, Lucknow, India.
Presence of spondyloarthropathy and its clinical profile in patients with hypoparathyroidism.
Clin Endocrinol (Oxf)
February 2008
Department of Endocrinology and Metabolism, All India Institute of Medical Sciences, New Delhi 110029, India.
Background: Though spondyloarthropathy has been described in patients with sporadic idiopathic hypoparathyroidism (SIH), the clinical profile is not known.
Objectives: To describe the clinical profile including radiological features of spondyloarthropathy and prevalence of HLA-B27 allele in patients with hypoparathyroidism, and to identify any differences from ankylosing spondylitis.
Subjects And Methods: Clinical characteristics and radiographs of pelvis and spine were assessed in 40 consecutive patients with SIH.
Familial Mediterranean fever responds well to infliximab: single case experience.
Clin Rheumatol
February 2006
Division of Rheumatology, Department of Physical Medicine and Rehabilitation, Faculty of Medicine, Firat University, Elazig, Turkey.
The most common arthritic involvement in familial Mediterranean fever (FMF) is acute recurrent monoarthritis; however, sometimes spondyloarthropathy-like findings or typical ankylosing spondylitis may also ensue. Reported here is our favorable experience with infliximab in an FMF patient who had been resistant to colchicine and disease-modifying antirheumatic drugs (sulfasalazine and methotrexate) treatments. A 72-week follow-up of the patient yielded complete remission of the febrile abdominal episodes, and spondylitis responded well.
View Article and Find Full Text PDFArthritis in association with human immunodeficiency virus infection in Black African children: causal or coincidental?
Rheumatology (Oxford)
July 2005
Department of Paediatrics and Child Health, Nelson R. Mandela School of Medicine, University of KwaZulu Natal, Private Bag X7, Congella, 4013, South Africa.
Objectives: To compare human immunodeficiency virus (HIV)-infected and HIV-uninfected children with arthritis of unknown origin to determine whether the association between HIV infection and arthritis is causal or coincidental.
Method: Retrospective review of 132 children with arthritis who were tested for HIV infection.
Results: Thirty-five (27%) of the children were HIV infected and the male to female ratio was 2.
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