Results 51 to 60 of about 4,852,263 (194)
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.
Embong, Zunaina +5 more
core +1 more source
Antistreptolysin O Levels in Patients with Behcet’s Disease
Eurasian Journal of Medicine, 2019 Objective: Behcet’s disease is a multisystem inflammatory disorder, and its etiology has not been defined clearly yet. In this study, we aimed to investigate the antistreptolysin O (ASO) levels of patients with Behcet’s disease. Materials and Methods:
Hulya Uzkeser +4 more
doaj +1 more source
Rare vasculitis types and obstetric and neonatal outcomes – A population‐based study
International 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
Omics studies in Behçet’s disease
Purpose of review In this review, we aimed to highlight recent findings from “-omics” studies in Behçet’s disease. Recent findings Recent genomic studies in Behçet’s disease identified possible risk loci associated with Behçet’s disease related uveitis ...
Nowatzky, Johannes, ÖZGÜLER, YEŞİM
core +1 more source
JPGN 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
A Case of Azathioprine Induced Warfarin Resistance in Behçet’s Disease [PDF]
, 2015 Behçet’s disease is characterized by recurrent oral aphthous ulcers, genital ulcers, uveitis, and skin lesions. Thrombosis associated with vascular inflammation in patients with Behçet’s disease presents various clinical symptoms.
임동우 +3 more
core
Neuro‐Behçet's Disease and Psychiatric Disorders: From a Case Report to a Systematic Review
Brain and BehaviorBackground Behçet's disease is a chronic, relapsing systemic vasculitis that can affect multiple organ systems. Neurological involvement, known as neuro‐Behçet's disease, occurs in a subset of patients, while psychiatric manifestations—termed neuro ...
Jorge Renau +5 more
doaj +1 more source
High levels of endothelial progenitor cells and circulating endothelial cells in patients with Behçet's disease and their relationship to disease activity [PDF]
Anais Brasileiros de Dermatologia, 2019 : Background: Behçet's disease is a multisystemic vasculitis, associated with vascular endothelial dysfunction. Currently, the prognosis is unpredictable, because there is still no valid laboratory marker indicating the disease activity in Behçet's ...
Deniz Aksu Arica +5 more
doaj +1 more source
Juvenile Gangrenous Vasculitis of the Scrotum or Scrotum Lipschütz Ulcers
JEADV Clinical Practice, EarlyView.ABSTRACT Lipschütz genital ulcers are traditionally described in adolescent females and often linked to acute viral infections. Their male counterpart remains poorly characterised. We report a 59‐year‐old man with sudden onset of unilateral necrotic ulcers on the scrotum and inguinal region following a brief febrile episode and mild pharyngitis ...
Francesco Bellinato +2 more
wiley +1 more source