Vasculitis for Professionals
- General Information & Clinical Trials
- UKIVAS Vasculitis Registry
- Paediatric Vasculitis
- Guidelines - Treatment and Management & Advice
- Research and Education Funded by Vasculitis UK
- Research and Education Supported by Vasculitis UK
- Travel Bursaries for 2019
- Research Papers
- Book Reviews
- Videos & Podcasts
- Guide to Newsletter/Journal Articles
- Rare Autoimmune Rheumatic Diseases Alliance (RAIRDA)
The Vasculitis Website: for Professionals
Call for Research Grants - November 2018Vasculitis UK has recently announced a Call for Proporsals for research funding. Full details can be found here
Primary Systemic Vasculitis is a rare disease. The different types of systemic vasculitis are rare and variable in presentation, not easy to recognise, difficult to diagnose and frequently difficult to treat.
Delayed diagnosis may result in death or disability. This website offers quick and easy access to reliable clinical information for busy clinicians.
This website is intended primarily to inform, advise, help and support those suffering from vasculitis. Therefore, much of the clinical content is written in language that lay people can understand.
However we recognise that many clinicians can have only limited exposure to and experience of vasculitic disease. So there is also a wealth of reliable clinical information here about vasculitis in general, with details of clinical signs and symptoms of specific types of vasculitis, diagnostic tools and treatment guidelines.
A large part of the clinical content of this website has been taken from the:
Additional material has been provided by: Dr Nicola Ambrose, Dr Paul Brogan, Dr Catherine Guly, Prof Dorian Haskard, Dr Marcos Martinez Del Pero and Prof Justin Mason.
Listed are the most relevant papers on vasculitis diagnosis and treatment, with both lay and professional summaries of the content of each, for rapid and easy access. There are also details of some very rare types of vasculitis that are not readily found in textbooks.