Results 21 to 30 of about 15,430 (233)
Egy ritkán felismert ritka betegség: a Behcet-kór [PDF]
, 2013 A Behcet-kór multiszisztémás autoimmun betegség változatos klinikai megjelenési tünetekkel. Hazánkban a Behcet-kór a ritka betegségek közé tartozik, a témával foglalkozó közlemények száma elenyésző.
Dohán, Judit +3 more
core +1 more source
Could Mean Platelet Volume Be Used as A Marker for Oral Aphthae and Activity of Behçet’s Disease?
İstanbul Medical Journal, 2016 Objective: Behçet’s disease is a common inflammatory disease in our country. We aimed to determine whether mean platelet volume can be used as a marker for oral aphthae and the activity of Behçet’s disease.Methods: Between 04/01/2010 and 30/07/2010, 78 ...
Okan Dikker +5 more
doaj +1 more source
Audio-vestibular symptoms in systemic autoimmune diseases [PDF]
, 2018 Immune-mediated inner ear disease can be primary, when the autoimmune response is against the inner ear, or secondary. The latter is characterized by the involvement of the ear in the presence of systemic autoimmune conditions. Sensorineural hearing loss
Adelchi, Croce +7 more
core +1 more source
Low Level Laser Therapy to Reduce Recurrent Oral Ulcers in Behçet’s Disease
Case Reports in Dentistry, 2016 Behçet’s disease (BD) is a chronic, relapsing multisystemic vascular condition. Behçet’s disease was described by Hulusi Behçet in 1937. This rare multisystem relapsing-remitting inflammatory disease is poorly understood but is thought to be an ...
D. B. Gandhi Babu +4 more
doaj +1 more source
Journal of Medical Case Reports, 2011 Introduction The risk that patients with Behçet's disease will develop thrombotic complications has been previously described. Although it is distributed worldwide, Behçet's disease is rare in the Americas and Europe.
Évora Paulo RB +4 more
doaj +1 more source
Asymptomatic giant coronary aneurysm in an adolescent with Behcet's syndrome [PDF]
, 2012 Objective Behcet's is an idiopathic multi-organ syndrome, which may have onset during childhood. Vascular involvement is uncommon, with rarely reported coronary aneurysm formation.
Philip J Kahn +4 more
core +2 more sources
Paediatric Behçet's disease: a UK tertiary centre experience [PDF]
, 2016 There are currently limited data regarding paediatric Behçet's disease (BD), particularly in the UK. We describe the clinical spectrum, treatment and outcome of BD, and explore the relative sensitivities of the criteria for the diagnosis of BD in a UK ...
Ambrose, N +4 more
core +1 more source
Behçet's Disease (Adamantiades-Behçet's Disease)
Clinical and Developmental Immunology, 2011 Adamantiades-Behçet's disease (ABD) is characterized by starting with oral aphthous ulceration and developing of the systemic involvements. The pathogenesis of ABD is closely correlated with the genetic factors and the triggering factors which acquire ...
Fumio Kaneko +7 more
doaj +1 more source
High prevalence of Helicobacter pylori infection in Behcet’s disease [PDF]
, 2014 Background: Behcet’s disease (BD) is a multisystem disease of unknown etiology. There are several clues which may indicate an ethiopathogenesis role for Helicobacter pylori infection in this disease.
Aflaki, Elham +4 more
core +1 more source
International medical case reports journal, 2019 To report a case of Behcet's disease presented with bilateral hypopyon after sequential cataract surgery masquerading delayed onset post-operative endophthalmitis.A 53-year-old man with a history of sequential uneventful cataract surgeries came to our clinic with decreased vision (0.3 LogMAR) since 2 days ago and bilateral hypopyon in his both eyes ...
Mohammadpour,Mehrdad +2 more
openaire +4 more sources