Results 11 to 20 of about 1,148,121 (177)
Diagnosis and management of recurrent herpetiform stomatitis and Behçet syndrome like recurrent aphthous stomatitis herpetiform type [PDF]
Padjadjaran Journal of Dentistry, 2008 Recurrent Aphthous Stomatitis (RAS) is a common inflammatory condition of the oral mucosa. The aetiology of RAS remains unclear, yet there are several predisposing factors which could be involved in the onset of the lesion.
Endah Ayu Tri Wulandari +1 more
doaj +4 more sources
Anticoagulation in Behçet related intrathoracic vasculitis
Respiratory Medicine Case Reports, 2018 Behçet disease is a rare multisystem condition associated with HLA-B51 positivity that commonly afflicts individuals of Turkish or Middle Eastern descent, less than 10% of whom have pulmonary involvement.
Brandon Nokes +5 more
doaj +2 more sources
Relationship between dietary histamine intake and clinical parameters in Behçet syndrome
Gülhane Tıp DergisiAims: This study investigated histamine intake and its associations with clinical and biochemical findings in patients with Behçet syndrome. Methods: Patients with Behçet syndrome were prospectively enrolled using a cross-sectional, multicenter, and ...
Hüsna Ercin, Nesli Ersoy
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Behçet syndrome with eye involvement. [PDF]
Saudi J OphthalmolBehçet’s uveitis (BU) is a significant form of major organ involvement in Behçet syndrome and is associated with considerable morbidity. Ocular examination is crucial for diagnosing BS and detecting vitreous cells, even in asymptomatic patients.
Ucar D, Esatoglu SN.
europepmc +2 more sources
Behçet Syndrome: two cases between twins [PDF]
, 2023 | Introdução: A síndrome de Behçet é uma vasculite sistêmica auto inflamatória que ocorre predominantemente na Turquia, sendo mais rara nos países ocidentais.
Tosato Boldrini, Neide Aparecida +2 more
core +1 more source
The OMERACT Core Set of Domains for Outcome Measures in Behçet Syndrome [PDF]
, 2020 OBJECTIVE: There is an unmet need for reliable, validated, and widely-accepted outcome measures for randomized clinical trials in Behçet syndrome (BS).
MUMCU, GONCA, DİRESKENELİ, RAFİ HANER
core +3 more sources
Outcome measures in Behçet syndrome
, 2023 Disease assessment has been challenging in Behçet syndrome due to the heterogeneous disease course and multiorgan involvement with variable treatment response.
Yazici, Yusuf +3 more
core +1 more source
, 2021 Behçet syndrome is a systemic vasculitis with an unknown aetiology affecting the small and large vessels of the venous and arterial systems. The presence of symptom clusters, regional differences in disease expression and similarities with, for example ...
천재희
core +1 more source
Intracardiac thrombus in Behçet´s disease: a rare case in Morrocco
The Pan African Medical Journal, 2020 Behçet´s syndrome is a systemic inflammatory disease generally presented with the triad of uveitis, oral and genital ulcers. However, it may present with gastrointestinal, central nervous system, skin and vascular disease manifestations.
Younes Amchich +5 more
doaj +1 more source
A novel KIF11 mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous family. [PDF]
, 2012 Microcephaly–lymphedema–chorioretinal dysplasia (MLCRD) syndrome is a rare syndrome that was first described in 1992. Characteristic craniofacial features include severe microcephaly, upslanting palpebral fissures, prominent ears, a broad nose, and a ...
Ostergaard, P +27 more
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