Cytochrome P2 polymorphisms and susceptibility to scleroderma following exposure to organic solvents

A Povey, MJ Guppy, M Wood, C Knight… - Arthritis & …, 2001 - Wiley Online Library
Objective To determine whether there are specific cytochrome P450 (CYP2) alleles that
increase susceptibility to scleroderma in individuals who have been exposed to organic …

[HTML][HTML] Role of telomere shortening in anticipation of inflammatory bowel disease

B Truta, E Wohler, N Sobreira, LW Datta… - World Journal of …, 2020 - ncbi.nlm.nih.gov
BACKGROUND The existence of genetic anticipation has been long disputed in
inflammatory bowel disease (IBD) in the absence of the explanatory mechanism. AIM To …

Genetics and Epigenetics Mechanism in the Pathogenesis of Behçet's Disease

JS Muhammad, M Ishaq… - Current rheumatology …, 2019 - ingentaconnect.com
Background: Behçet's Disease (BD) is characterized by numerous systemic manifestations
and is known for its ability to affect both, arteries and the veins. However, the etiology of BD …

Genetic anticipation in rheumatoid arthritis in Europe. European Consortium on Rheumatoid Arthritis Families.

TR Radstake, P Barrera, MJ Albers… - The Journal of …, 2001 - jrheum.org
OBJECTIVE: To investigate whether there is evidence for genetic anticipation in rheumatoid
arthritis (RA) in Europe. METHODS: Cross sectional comparison of data from all affected …

Genetics of Behçet's disease

A Gül, GR Wallace - Behçet Syndrome, 2020 - Springer
Behçet's disease (BD) is a multifactorial disease with a strong genetic background. Higher
frequencies of patients with a positive family history for BD were reported from the Middle …

[HTML][HTML] Clinical manifestations of Behçet's syndrome: a single-center cohort of 777 patients

C Gürbüz, DY Kehribar, M Özgen - European Journal of …, 2021 - ncbi.nlm.nih.gov
Objective: Behçet's syndrome (BS) is a multisystem variable vessel vasculitis characterized
by skin-mucosal lesions. It can also involve the eyes, blood vessels, joints, gastrointestinal …

Copy number variations and gene polymorphisms of Complement components in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome

D Xu, S Hou, J Zhang, Y Jiang, A Kijlstra, P Yang - Scientific Reports, 2015 - nature.com
Complement is involved in many immune-mediated diseases. However, the association of
its copy number variations (CNVs) and polymorphisms with Behcet's disease (BD) and Vogt …

The distinct expressions of interleukin-15 and interleukin-15 receptor α in Behçet's disease

JY Choe, H Lee, SG Kim, MJ Kim, SH Park… - Rheumatology …, 2013 - Springer
Abstract Interleukin-15 (IL-15) is a pleotrophic cytokine that is involved in the pathogenesis
of diverse inflammatory rheumatic diseases. The aims of this study were to compare serum …

Behçet's syndrome: the cerrahpasa experience

H Yazici, I Fresko, V Hamuryudan, C Mat… - … : Current Issues in …, 1999 - Springer
Behçet's syndrome (BS) is a systemic vasculitis of unknown etiology. There are several
reasons for doubting a primary autoimmune pathogenesis of this condition. Recent …

Behcet disease in children

N Kitaichi, S Ohno - International Ophthalmology Clinics, 2008 - journals.lww.com
Uveitis in childhood is uncommon. The annual incidence of noninfectious uveitis has been
estimated to be 4 to 7/100,000 children per year. 1–3 Unlike adults, juvenile idiopathic …