Results 51 to 60 of about 2,441 (231)
IN TIME VARIATION OF PATHERGY PHENOMENON IN BEHCET'S DISEASE [PDF]
Acta Medica Iranica, 1996 The pathergy phenomenon (PP) is one of the hallmarks of Behcet's Disease (BD). It has been reported to be positive from 17.5% to 83% of cases in different studies.
C. Chams F. Davatchi +4 more
doaj
AIF-1 gene does not confer susceptibility to Behçet's disease: Analysis of extended haplotypes in Sardinian population [PDF]
, 2018 Background BehcEet's disease (BD) is a polygenic immune-mediated disorder characterized by a close association with the HLA-B∗51 allele. The HLA region has a strong linkage disequilibrium (LD) and carries several genetic variants (e.g. MIC-A, TNF-α genes)
Angioni, Mm +11 more
core +3 more sources
Ulcus vulvae acutum — A case of genital ulcers in adolescent girl
Case Reports in Women's Health, 2016 Ulcus vulvae acutum is a rare clinical condition characterized by the presence of multiple acute painful genital ulcers of non-venereal origin associated with systemic symptoms in young women. The aetiopathogenesis of the disease is not fully understood,
Daniela Visentin +7 more
doaj +1 more source
European Journal of Dental Education, EarlyView.ABSTRACT Aim To compare the item difficulty and discriminative index of multiple‐choice questions (MCQs) generated by ChatGPT with those created by dental educators, based on the performance of dental students in a real exam setting. Materials and Methods A total of 40 MCQs—20 generated by ChatGPT 4.0 and 20 by dental educators—were developed based on ...
Nezaket Ezgi Özer +4 more
wiley +1 more source
Severe panuveitis in neuro-Behçet’s disease in Malaysia: a case series [PDF]
, 2017 Behçet’s disease (BD) is a multisystemic disease that is very rare in Malaysia. About 5% of patients develop central nervous system involvement, termed neuro-Behçet’s.
Ahmad Tajudin, Liza Sharmini +5 more
core
Bullous pyoderma gangrenosum and myelodysplastic syndrome [PDF]
, 2006 Pyoderma gangrenosum can present as a cutaneous manifestation of paraneoplastic syndromes. A case of bullous pyoderma gangrenosum associated with bicytopenia is described.
Almeida, Fernando Augusto De +7 more
core +4 more sources
Rheumatology, 2019 Behçet’s disease is a multi-systemic vasculitis which is characterized by recurrent oral and genital ulceration with positive pathergy test. These features may also be seen in various hematological malignancies. In patients with leukemia who present with
Ashish Sharma +4 more
doaj +1 more source
Bilateral Retrobulbar Optic Neuritis as the First Manifestation of Neuro-Behçet Disease
Case Reports in Rheumatology, 2020 Background. Behçet disease (BD) is a polygenic and chronic autoinflammatory multisystem vasculitis. Acute optic neuritis has been rarely reported in patients with BD, especially in children. Case Presentation. We reported an 8-year-old girl with a sudden
Mohsen Jari +2 more
doaj +1 more source
TNF Inhibitor Therapy in Corticosteroid‐Resistant or ‐Dependent Pediatric Neutrophilic Dermatosis
Pediatric Dermatology, EarlyView.ABSTRACT Neutrophilic dermatoses are rare in children. Systemic corticosteroids are the first‐line treatment, but guidelines for second‐line therapies are lacking. We report five cases of children with systemic steroid‐resistant/dependent neutrophilic dermatoses, successfully treated with tumor necrosis factor inhibitors.
Laure Chêne +7 more
wiley +1 more source
Challenging cases discussed by experts: retinal vasculitis following coinfection with HIV and syphilis [PDF]
, 2011 A patient with HIV and syphilis presents with bilateral retinal vasculitis and recurrent vitreous hemorrhage.
Thomas Albini +2 more
core +1 more source