Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Deva Situnayake"'
Autor:
Niloy Rahman, Eshan Senanayake, Jorge Mascaro, Deva Situnayake, Ehab S. Bishay, Akshay J. Patel
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 18, Iss 1, Pp 1-5 (2023)
Abstract Background Behcet’s disease is a multi-system inflammatory disorder. A small subset of patients with Behcet’s develop relapsing polychondritis which is classified as a separate disease known as Mouth and Genital ulcers with inflamed cart
Externí odkaz:
https://doaj.org/article/4e57fec052614009870c1dd2e957ac95
Publikováno v:
Rheumatology. 62
Background/Aims Behçet’s Syndrome is considered rare in the UK. Prevalence estimates range from 0.64 to14.61 per 100 000 population. Here we explore validity of HES ICD-10 codes for BS using Birmingham Centre of excellence (BCoE) data as reference
Publikováno v:
General Hospital Psychiatry. 70:103-108
To measure health utilities Time Trade-Off (TTO) and Standard Gamble (SG) in Behcet's disease (BD), and explore the interrelationships with EQ-5D-5L, disease activity, depression, anxiety and fatigue.TTO, SG, EQ-5D-5L, EQ VAS, depression (PHQ-9), anx
Autor:
Priyanka Chandratre, Joht Chandan, Manrup Hunjan, Nigel Trudgill, Robert Moots, Farida Fortune, Rohan Deva Situnayake
Publikováno v:
Rheumatology. 61
Background/Aims Behçet’s disease (BD) is a rare multisystem auto-inflammatory disorder. In England the incidence is estimated between 0.38 per 100,000 in the population, however, the actual incidence of BD in U.K. is unknown. The prevalence is est
Autor:
Anuradhaa Subramanian, Lorraine Harper, Krishna Gokhale, Deva Situnayake, George Gkoutos, Krishnarajah Nirantharakumar, Christopher D. Buckley, Karim Raza, Joht Singh Chandan, Tom Thomas, Priyanka Chandratre
Publikováno v:
Rheumatology. 59:2785-2795
Objectives The epidemiology of Behçet’s disease (BD) has not been well characterized in the UK. Evidence on the risk of cardiovascular disease, thromboembolic disease and mortality in patients with BD compared with the general population is scarce
Publikováno v:
Rheumatology Advances in Practice
Introduction Behçet’s Disease (BD) is a complex, multisystem auto-inflammatory disorder. The most frequent manifestations are oral aphthous ulcers, genital ulcers and uveitis. Vascular involvement is less common but one of the major causes of mort
Publikováno v:
Rheumatology. 58
Publikováno v:
THURSDAY, 14 JUNE 2018.
Background Geographical variations in genotype and phenotype of Behcet’s syndrome (BS) are reported.1,2 Previous meta-analysis of international cohorts has highlighted differences in clinical manifestations of BS by gender.3 A comparison of BS clin
Autor:
Steve Powell, Debbie Mitton, David Carruthers, Sue Protheroe, Deva Situnayake, Tauny Southwood, Eslam Al-Abadi, Vishal Paisal
Publikováno v:
Rheumatology. 56
Autor:
S. Powell, David Carruthers, T Southwood, Deva Situnayake, V Paisal, D. Mitton, S Protheroe, E Al-Abadi
Publikováno v:
Poster Presentations.
Background Behcet Disease (BD) is rarely reported in children. It a systemic inflammatory condition characterised by autoinflammatory and vasculitic clinical features including recurrent oral aphthosis, genital ulceration, skin, eye, neurological and