Results 11 to 20 of about 7,353 (153)

A coronary artery aneurysm revealing a Behçet´s disease: a case report

open access: yesThe Pan African Medical Journal, 2020
Behçet´s disease (BD) is a multisystemic chronic vasculitis characterized by its clinical polymorphism. It concerns mainly young men and generally appears between the third and the fourth decades.
Sameh Ben Farhat, Mehdi Slim
doaj   +1 more source

Recent Insights into the Management of Behçet Syndrome

open access: yesJournal of Inflammation Research, 2021
Yesim Ozguler, Ayse Ozdede, Gulen Hatemi Istanbul University-Cerrahpasa, Cerrahpasa Medical Faculty, Department of Internal Medicine, Division of Rheumatology and Behçet Disease Research Center, Istanbul, TurkeyCorrespondence: Gulen HatemiIstanbul ...
Ozguler Y, Ozdede A, Hatemi G
doaj  

Anticoagulation in Behçet related intrathoracic vasculitis

open access: yesRespiratory 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   +1 more source

Real-world effectiveness and safety of adalimumab in Korean patients with intestinal Behcet’s disease: a Korean Association for the Study of Intestinal Diseases (KASID) multicenter study [PDF]

open access: yesThe Korean Journal of Internal Medicine, 2023
Background/Aims The short- and long-term effects of adalimumab (ADA) on Korean patients with intestinal Behcet’s disease (BD) for remain unclear. Therefore, a multicenter study was performed to evaluate the efficacy and safety of ADA in Korean patients ...
Seung Bum Lee   +11 more
doaj   +1 more source

Diagnosis and management of recurrent herpetiform stomatitis and Behçet syndrome like recurrent aphthous stomatitis herpetiform type

open access: yesPadjadjaran 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   +1 more source

Refractory neuro-Sweet disease successfully treated with tocilizumab and mycophenolate mofetil [PDF]

open access: yesEncephalitis, 2021
Sweet syndrome, or acute febrile neutrophilic dermatosis, is mainly a dermatologic condition presenting with erythematous plaques; however, neutrophils infiltrate multiple systems. Neuro-Sweet disease is a neurological manifestation of Sweet syndrome and
Sungeun Hwang   +7 more
doaj   +1 more source

The evaluation of epicardial adipose tissue and carotid intima-media thickness in patients with Behçet’s disease [PDF]

open access: yesVojnosanitetski Pregled, 2022
Background/Aim. Epidemiological studies indicate that cardiovascular disease (CVD) is common in almost all patients diagnosed with autoimmune disease. This study aimed to examine whether epicardial adipose tissue (EAT) thickness (EATT) and carotid intima-
Sağlam Gonca   +2 more
doaj   +1 more source

Multimodal imaging in pediatric uveitis

open access: yesTherapeutic Advances in Ophthalmology, 2021
Pediatric uveitis accounts for up to 10% of all uveitis cases, so special attention must be paid to ensure early diagnosis as well as treatment and follow-up of these young patients in order to decrease the risk of possible ocular complications and ...
Fitz Gerald I. Diala   +3 more
doaj   +1 more source

Analysis of clinical and immunological characteristics of nervous system involvement in Behcet's disease

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2021
Objective To investigate the clinical features and risk factors of nervous system involvement in Behcet's disease (BD). Methods A total of 74 BD patients who were admitted to Peking University People's Hospital from January 2013 to January 2019 were ...
MAO Yu⁃jing, LIU Tian
doaj   +1 more source

Behçet Disease-Like Symptoms with a Novel COPA Mutation

open access: yesCase Reports in Genetics, 2020
COPA syndrome is a recently described autosomal dominant disorder with key immune dysregulation caused by defects within the COPA gene. These mutations lead to endoplasmic reticulum stress and autoimmune response with upregulation of Th17 cytokines.
E. Anderson   +4 more
doaj   +1 more source

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