Results 51 to 60 of about 1,148,121 (177)

Doença de Behçet ocular: a nossa realidade

open access: yesRevista Brasileira de Oftalmologia
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

open access: yesLung India, 2011
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

open access: yesArthritis &Rheumatology, Accepted Article.
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]

open access: yes, 2022
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

open access: yesBMC Research Notes, 2021
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

open access: yesInternational Journal of Gynecology &Obstetrics, EarlyView.
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

The genetic landscape of congenital diarrheas and very early onset inflammatory bowel disease in the Middle East

open access: yesJPGN Reports, EarlyView.
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

open access: yesO Mundo da Saúde, 2010
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

open access: yesTürk Oftalmoloji Dergisi
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

Inflammation Unchecked: Concurrent Kawasaki Disease and Stevens‐Johnson Syndrome in an 18‐Month‐Old Child

open access: yes
Arthritis Care &Research, EarlyView.
Catherine Deffendall   +6 more
wiley   +1 more source

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