Current concepts in the etiology and treatment of Behçet disease

C Evereklioglu - Survey of ophthalmology, 2005 - Elsevier
Behçet disease is an idiopathic, multisystem, chronic, and recurrent disease characterized
by exacerbations alternating with phases of quiescence, episodic panuveitis, and …

The multiple faces of Behçet's disease and its aetiological factors

M Önder, MA Gürer - Journal of the European Academy of …, 2001 - Wiley Online Library
Behçet's disease (BD) is a chronic, inflammatory multisystemic condition of unknown
aetiology. It is clinically characterized by recurrent orogenital ulcerations and skin eruptions; …

Familial aggregation of Behcet's disease in Turkey

A Gül, M Inanç, L Öcal, O Aral, M Koniçe - Annals of the rheumatic …, 2000 - ard.bmj.com
OBJECTIVE Familial aggregation of Behçet's disease has been reported previously. The
current study aimed at investigating the sibling recurrence risk ratio (λs) for Behçet's disease …

Epidemiology of Behçet disease

M Khairallah, M Accorinti, C Muccioli… - Ocular immunology …, 2012 - Taylor & Francis
Behçet disease (BD) is a multisystem inflammatory disorder that is an important cause of
morbidity worldwide. BD is most common along the ancient “Silk Road” route in the Far East …

Behçet's disease in the Middle East

T Saylan, C Mat, I Fresko, M MelikoĞlu - Clinics in Dermatology, 1999 - cidjournal.com
Behçet's disease (BD), originally described as oral and genital ulcers and uveitis, 1 is a
vasculitis that can involve any organ system. It is a commonly encountered health problem in …

Behçet's disease as a systemic disease

MC Mat, A Sevim, İ Fresko, Y Tüzün - Clinics in dermatology, 2014 - Elsevier
Behçet's disease usually begins with cutaneous manifestations, such as recurrent aphthous
stomatitis, genital ulcers, erythema nodosum-like lesions, papulopustular findings, and …

Behçet disease, familial Mediterranean fever and MEFV variations: more than just an association

E Seyahi, S Ugurlu, S Amikishiyev, A Gul - Clinical Immunology, 2023 - Elsevier
Behçet disease (BD) and familial Mediterranean fever (FMF) are two inflammatory disorders
that share many features including historical background, ethnical distribution and …

[PDF][PDF] The prevalence of familial Mediterranean fever in the Turkish province of Denizli: a field study with a zero patient design

V Çobankara, G Fidan, T Turk, M Zencir… - Clinical and …, 2004 - clinexprheumatol.org
Objective. This study had two aims:(1) to investigate the prevalence of familial
Mediterranean fever (FMF) and B eh ç et's disease (BD) in school students in Denizli, a …

[HTML][HTML] Neutrophilic dermatoses: part I

RR Bonamigo, F Razera, GS Olm - Anais Brasileiros de Dermatologia, 2011 - SciELO Brasil
The authors present a review of neutrophilic dermatoses that have great impact on the
health of patients: Sweet syndrome, pyoderma gangrenosum, Behçet's disease and …

Behçet hastalığı

E ARCA, AR GÜR - Turkiye Klinikleri Journal of Medical …, 2003 - turkiyeklinikleri.com
Behçet hastalığı etiyolojisi bilinmeyen kronik, immüno-inflamatuar multisistemik bir
hastalıktır. Özellikle ülkemizde, Akdeniz ülkelerinde ve Japonya'da sık görülür …