Results 51 to 60 of about 1,148,121 (177)
Doença de Behçet ocular: a nossa realidade
Resumo Objetivo: A doença de Behçet é uma vasculite inflamatória sistémica, de etiologia desconhecida. Pode atingir virtualmente todos os sistemas, sendo as manifestações oculares comuns.
Inês Coutinho +6 more
doaj +1 more source
Hughes-Stovin syndrome: A rare cause of hemoptysis
Multiple pulmonary artery aneurysms are seen along with venous thrombosis in Hughes-Stovin syndrome, which many investigators believe is an incomplete form of Behcet′s disease.
Naseer A Choh +4 more
doaj +1 more source
Human Monocytic Models Reveal Genotype‐Dependent Inflammatory Programs in VEXAS Syndrome
Objectives VEXAS syndrome is a severe X‐linked autoinflammatory disorder caused by somatic mutations in ubiquitin‐like modifier activating enzyme 1 (UBA1), with clinical outcomes that vary by UBA1 genotype. We aimed to elucidate genotype‐specific inflammatory programs and identify potential therapeutic targets.
Kana Higashitani +10 more
wiley +1 more source
Neuro-Behçet: diagnóstico diferencial de enfermedades desmielinizantes [PDF]
The Behçet´s disease (BD) is an inflammatory multisystemic vasculitis of unknown etiology and is classified as a rare disease in the USA and European countries.
Rivera Sandoval, Natalia +3 more
core +1 more source
Using hierarchical similarity to examine the genetics of Behçet’s disease
Objective Behçet’s disease (BD) is a multisystem inflammatory disease that affects patients along the historic silk road. Thus far, the pathogenesis of the disease has proved elusive due to the complex genetic interactions of the disease.
Samuel J. Shenoi, Erich J. Baker
doaj +1 more source
Rare vasculitis types and obstetric and neonatal outcomes – A population‐based study
Abstract Objective Vasculitis is an infrequent pathology among reproductive‐aged women. While data exists regarding pregnancy outcomes in the more common vasculitis subtypes, data is limited regarding these outcomes in rare vasculitis subtypes. We aimed to compare pregnancy and perinatal outcomes between women who suffered from rare types of vasculitis
Uri Amikam +4 more
wiley +1 more source
Abstract Objectives Monogenic causes of congenital diarrheas and enteropathies (CoDE) and very early onset inflammatory bowel disease (VEOIBD) are mostly recessive and therefore more prevalent in populations with increased consanguinity rates. To assess the genetic basis of these disorders in a likely high‐prevalence population, we established a multi ...
Lily Gillette +21 more
wiley +1 more source
Physiotherapeutic rehabilitation in Behçet Syndrome: a literature survey
Behçet syndrome (BS) is a multi-systemic inflammatory affection of vascular incidence and unknown cause, characterized by recurrent mouth and genital ulcers, uveitis, cutaneous injuries, articulation and neuromuscular incidence.
Maurício Bezerra da Silva +3 more
doaj
Treatment of Behçet Uveitis in Türkiye
Objectives: Behçet uveitis (BU) is a potentially blinding disorder. The main determinant of visual prognosis is early and appropriate treatment that provides rapid suppression of inflammatory attacks, control of subclinical inflammation, and prevention ...
Pınar Çakar Özdal +4 more
doaj +1 more source

