Familial aggregation in Behçet's disease: high frequency in siblings and parents of pediatric probands

I Koné-Paut, I Geisler, B Wechsler, S Ozen… - The Journal of …, 1999 - Elsevier
Objective: To examine familial aggregation of Behçet's disease (BD) in pediatric compared
with non-pediatric patients. Methods: A retrospective study was conducted to analyze data …

Behçet syndrome: is it one condition?

H Yazici, S Ugurlu, E Seyahi - Clinical reviews in allergy & immunology, 2012 - Springer
Behçet's syndrome (BS) is a disease of unknown etiology, and as such, there have been
efforts to classify BS within the popular nosological identities of the times such as …

Pathogenesis of Adamantiades-Behçet's disease

CC Zouboulis, T May - Medical microbiology and immunology, 2003 - Springer
Abstract The aetiology of Adamantiades-Behçet's disease remains unknown and its
pathogenesis is not fully understood. Linked intrinsic and extrinsic factors are thought to …

Whole‐genome screening for susceptibility genes in multicase families with Behçet's disease

J Karasneh, A Gül, WE Ollier, AJ Silman… - Arthritis & …, 2005 - Wiley Online Library
Objective Behçet's disease is generally considered to be a multifactorial disease with
important genetic and environmental components. A strong association between an HLA …

Clinical characteristics of pediatric-onset neuro-Behçet disease

D Uluduz, M Kürtüncü, Z Yapıcı, E Seyahi… - Neurology, 2011 - AAN Enterprises
Objectives: Neurologic involvement in the pediatric population with Behçet disease (BD) is
limited to case reports. The aim of this study is to examine the frequency and type of …

[PDF][PDF] Onset signs, clinical course, prognosis, treatment and outcome of adult patients with Adamantiades-Behçet's disease in Greece

CC Zouboulis, G Vaiopoulos… - Clinical and …, 2003 - researchgate.net
Objectives. To examine the onset signs, clinical cours e, p rog nosis, t re at ment and
outcome of A damantiades-B ehç et's disease in adult Greek pat ients during a 10-year …

Behçet disease

H Yazici, S Yurdakul… - Current Opinion in …, 2001 - journals.lww.com
Central nervous system involvement in Behçet disease (BD) may be either parenchymal or
nonparenchymal. Abnormal cerebrospinal fluid findings and parenchymal involvement are …

Behcet's disease in UK children: clinical features and treatment including thalidomide

JA Kari, V Shah, MJ Dillon - Rheumatology, 2001 - academic.oup.com
Objective. To study the clinical spectrum of Behçet's disease (BD) in childhood, and to report
our experience of using thalidomide. Method. Ten children, diagnosed with BD, were …

MicroRNA-146a and Ets-1 gene polymorphisms in ocular Behcet's disease and Vogt–Koyanagi–Harada syndrome

Q Zhou, S Hou, L Liang, X Li, X Tan, L Wei… - Annals of the …, 2014 - ard.bmj.com
Aim MicroRNA-146a (miR-146a) is involved in certain immune-mediated diseases.
Transcription factor Ets-1 strongly affects miR-146a promoter activity and directly regulates …

Lack of association of HLA‐B*51 with a severe disease course in Behçet's disease

A Gül, FA Uyar, M Inanc, L Öcal, I Tugal‐Tutkun… - …, 2001 - academic.oup.com
Objective. To investigate the previously reported association of HLA‐B51 with the
manifestations and severity of Behçet's disease (BD). Methods. The study group consisted of …