Results 211 to 220 of about 148,632 (315)

Evolving treatments for Sjögren disease: current approaches and emerging targets

Internal Medicine Journal, EarlyView.
Abstract Sjögren disease (SjD) is a prevalent systemic autoimmune condition characterised by exocrine gland dysfunction, systemic inflammation and heterogeneous organ involvement. Current management remains largely symptomatic, with no approved disease‐modifying therapies available and substantial unmet clinical need. However, advances in understanding
Mansi Bhurani, Adrian Y. S. Lee, Maureen Rischmueller, Alberta Hoi   +3 more
wiley   +1 more source

IgA Vasculitis Presenting As Isolated Monoarthritis Mimicking Transient Synovitis: A Diagnostic Challenge With Delayed Purpura. [PDF]

Cureus
Sadiq SB, Ashok V, Saidu AY.
europepmc   +1 more source

Olaparib‐associated cutaneous vasculitis in a patient with breast cancer

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Marcial Álvarez‐Salafranca, Teresa Puértolas, Adrián Diago, María Carmen Gómez‐Mateo   +3 more
wiley   +1 more source

Experience of Australian rheumatologists managing polymyalgia rheumatica: results from a national survey

Internal Medicine Journal, EarlyView.
Abstract Background Polymyalgia rheumatica is the commonest inflammatory condition affecting adults over 50 years of age, however it has been under‐researched and management varies in everyday clinical practice. Aim This national survey of rheumatologists and trainees managing polymyalgia rheumatica (PMR) in Australia sought to determine current ...
Jessica L. Leung, Victor Yang, Jem V. Ninan, Carlee Ruediger, David F. L. Liew, Russell R. C. Buchanan, Helen I. Keen, Catherine L. Hill, Claire E. Owen   +8 more
wiley   +1 more source

Quantitative assessment of intrapulmonary vessel volume by CTPA in vasculitis patients with pulmonary vascular involvement. [PDF]

BMC Med Imaging
Ming Y, Piao S, Zhao R, Wang J, Liao Z, Song L, Xiao R, Zhao R, Ma Z, Li B, Zheng F, Song W.   +11 more
europepmc   +1 more source

Australian clinical practice guideline: diagnosis and treatment of idiopathic multicentric Castleman disease

Internal Medicine Journal, EarlyView.
Abstract Idiopathic multicentric Castleman disease (iMCD) is a rare condition. The pathogenesis is incompletely understood; however, interleukin‐6 (IL‐6) is a major mediator. The clinical presentation is heterogeneous, from mild constitutional symptoms to severe multi‐organ failure.
Dipti Talaulikar, Jun Yen Ng, Adam Bryant, Annmarie Bosco, Hugh C. Caterson, Pratyush Giri, Pravin Hissaria, Simon J. Harrison, Stephen Lade, Connull Leslie, Jacinta Perram, H. Miles Prince, Dejan Radeski, Maureen Rischmueller, Craig Wallington‐Gates, Nicholas Weber, Alberta Hoi   +16 more
wiley   +1 more source

Case Report: Toxocariasis as a rare trigger of vasculitis: a case-based review. [PDF]

Front Immunol
Radovic S, Plavsic A, Miskovic R, Drazic A, Todorovic M, Pavlovic IO, Karic U, Popovic D, Micev M, Arandjelovic S.   +9 more
europepmc   +1 more source

CUTANEOUS VASCULITIS [PDF]

Medical Journal Armed Forces India, 1994
openaire   +2 more sources

When to consider an inborn error of immunity: clues for physicians

Internal Medicine Journal, EarlyView.
Abstract The term inborn errors of immunity (IEIs) refers to the rapidly expanding group of genetic disorders causing dysregulation of the immune system. With improved genetic testing in recent years, the number of defined IEIs and their range of phenotypic presentations has grown vastly, with more than 550 IEIs now described.
Meera Thangarajah, Lucinda J. Berglund
wiley   +1 more source

Toward a Revised Definition of Thrombotic Microangiopathy

Kidney International Reports
Sjoerd A.M.E.G. Timmermans, Daan P.C. van Doorn, Pieter van Paassen   +2 more
doaj   +1 more source