Results 1 to 10 of about 7,353 (153)
Immunogenicity of Infliximab Among Patients With Behçet Syndrome: A Controlled Study [PDF]
Frontiers in Immunology, 2020 BackgroundImmunogenicity of tumor necrosis factor alpha inhibitors (TNFis) has been recognized as an important problem that may cause loss of efficacy and adverse events such as infusion reactions.
Sinem Nihal Esatoglu +10 more
doaj +2 more sources
Heat Shock Proteins in Behçet Syndrome [PDF]
Balkan Medical Journal, 2023 Behçet syndrome (BS) is a systemic vasculitis of unknown etiology that affects the skin, mucosa, joints, eyes, central nervous system, gastrointestinal system, arteries, and veins.
Aslı Kıymet Kireçtepe Aydın +1 more
doaj +2 more sources
Bilateral optic neuritis as an atypical presentation of juvenile Behcet syndrome: A case report [PDF]
eNeurologicalSciBehcet syndrome is a systemic vasculitis characterized by relapsing uveitis, oral aphthous, and genital ulcers. We present a rare case of a 14-year-old male with juvenile Behcet syndrome (JBS) presenting as bilateral optic neuritis with oral aphthous ...
Armin Adibi +4 more
doaj +2 more sources
Surgical treatment of intestinal perforation in Behçet syndrome: anunusual presentation [PDF]
The Pan African Medical Journal, 2018 Behçet syndrome is a chronic, recurring, systemic disorder characterized by the histopathologic finding of nonspecific vasculitis in multiple organs.
Carla Sofia Vicente +1 more
doaj +2 more sources
Syndrome de Behçet associé à une néphropathie à Ig A [PDF]
The Pan African Medical Journal, 2015 Le syndrome de Behçet est une vascularite qui peut s'accompagner de plusieurs atteintes systémiques. Une atteinte rénale peut compliquer cette maladie. Les lésions rénales sont variées, les plus fréquentes sont l'amylose et la néphropathie à IgA. Patient
Madiha Mahfoudhi, Rym Goucha
doaj +2 more sources
Behçet Disease with Generalized Polymorphous Cutaneous Lesions: A Case Report
International Journal of Dermatology and Venerology, 2022 Introduction:. Behçet disease is a chronic multisystem vasculitis disease, however generalized polymorphous cutaneous lesions are uncommon. Here, we reported a case of Behçet disease with multiple parts of the body and complex lesions, which may lead to ...
Li-Wei Wang +4 more
doaj +1 more source
Management of Behcet’s syndrome
Rheumatology, 2020 AbstractBehcet’s syndrome (BS) is a variable vessel vasculitis with heterogeneous clinical features. Skin, mucosa and joint involvement can cause impairment of quality of life but do not cause permanent damage whereas untreated eye, vascular, nervous system and gastrointestinal system involvement can cause serious damage and even death.
Ertugrul Cagri Bolek, Omer Karadag
openaire +3 more sources
Long-term outcome after surgery in a patient with intestinal Behçet’s disease complicated by myelodysplastic syndrome and trisomy 8 [PDF]
Intestinal Research, 2020 Behçet’s disease (BD) is a multisystem inflammatory disease of unknown origin. Rarely, BD occurs together with myelodysplastic syndrome (MDS). Interestingly, it is speculated that these are not simple coexistence but that the etiology of intestinal BD is
Yuki Mori +10 more
doaj +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
Blepharoptosis in Behçet's Disease [PDF]
Archives of Aesthetic Plastic Surgery, 2016 Behçet's disease is a systemic chronic disease that occurs in tissues such as eyes, joints, organs and nerves, and it has been noted that symptoms may be observed in a variety of tissues.
So-Min Hwang +4 more
doaj +1 more source