Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Phani Kumar Devarasetti"'
Publikováno v:
European Journal of Rheumatology, Vol 10, Iss 4, Pp 169-175 (2023)
Externí odkaz:
https://doaj.org/article/b697bc8491e1400bbee79d22384f1b72
A Case of SAPHO Syndrome Complicated by Uveitis with Good Response to Both TNF Inhibitor and JAKinib
Publikováno v:
Case Reports in Rheumatology, Vol 2023 (2023)
Introduction. SAPHO (synovitis, acne, pustulosis, hyperostosis, and osteitis) syndrome is a rare autoinflammatory condition describing the constellation of inflammatory skin, bone, and joint manifestations which result in diagnostic difficulty and th
Externí odkaz:
https://doaj.org/article/3fec5b30083642b58ba8cbcd5453b75c
Publikováno v:
Indian Journal of Rheumatology, Vol 17, Iss 4, Pp 371-376 (2022)
Background: Diffuse alveolar hemorrhage (DAH) in systemic lupus erythematosus (SLE) is not very common but is associated with high mortality. No studies from India report on DAH in SLE. Materials and Methods: From the electronic database of SLE patie
Externí odkaz:
https://doaj.org/article/f97d3bb9ca954926baa7d7b60a65f40b
Publikováno v:
Indian Journal of Rheumatology, Vol 14, Iss 1, Pp 21-27 (2019)
Objective: The objective of this study is to measure plasma pentraxin 3 (PTX3) levels in Takayasu arteritis (TA) patients and to compare the accuracy of PTX3, high-sensitive C-reactive protein (hsCRP), and erythrocyte sedimentation rate (ESR) in dist
Externí odkaz:
https://doaj.org/article/044df7f434274245b4df977a260ae9f7
Publikováno v:
Indian Journal of Rheumatology, Vol 13, Iss 2, Pp 95-100 (2018)
Background: Studies on antineutrophil cytoplasmic autoantibodies-associated vasculitis (AAV) from India are scarce. The aim of the present study was to characterize the profile of AAV and experience with rituximab in ocular granulomatous with polyang
Externí odkaz:
https://doaj.org/article/c15ffb4e8ce5401fae56f556b3e7edd8
Publikováno v:
Rheumatology. 62
Background/Aims IgG4-related sclerosing disease is a systemic disease characterized by extensive IgG4-positive plasma cells and T-lymphocyte infiltration of various organs and tumour-like involvement of one or more exocrine glands or other extranodal
Publikováno v:
Indian Journal of Cardiovascular Disease in Women, Vol 06, Iss 02, Pp 100-105 (2021)
Systemic lupus erythematous–associated pulmonary arterial hypertension (SLE-PAH) is one of the important causes of mortality in lupus patients. Different autoantibodies are associated with SLE-PAH which can predict its future development. The objec
Publikováno v:
Rheumatology. 61
Background/Aims Short-term mortality in patients with SLE and high disease activity approaches 30% as reported by various studies. Raised serum interferon-alpha levels are observed in patients with active SLE. In mice studies interferon alpha(IFNα)
Publikováno v:
Lupus. 31(5)
Introduction: PRES, as a complication of juvenile lupus, is rarely reported in the literature. In this study, six juvenile lupus patients admitted with diagnosis of PRES were assessed on the basis of clinical characteristics, imaging findings, diseas
Autor:
Phani Kumar Devarasetti, Sreejitha K Sreesailam, Ramakrishna Narayanan, Subodh Gururani, Liza Rajasekhar
Publikováno v:
Journal of the Royal College of Physicians of Edinburgh. 50:295-298
Takayasu arteritis which is reported more commonly from Asia and in females can present as middle aortic syndrome with lower limb claudication. We present a case of a young male with Takayasu arteritis with middle aortic syndrome and Winslow pathway