Results 81 to 90 of about 1,239,123 (172)

Massive lower gastrointestinal bleeding associated with solitary rectal ulcer in a patient with Behçet’s disease

open access: yes, 2015
Solitary rectal ulcer syndrome is a rare benign disorder that has a wide range of clinical presentations and variable endoscopic fi ndings which makes it diffi cult to diagnose and treat.
Bes, C.   +7 more
core   +1 more source

Development and preliminary validation of the Behçet’s syndrome Overall Damage Index (BODI)

open access: yes, 2020
Objective To develop and validate the evidence-based and consensus-based Behçet’s Syndrome Overall Damage Index (BODI).Methods Starting from 120 literature-retrieved preliminary items, the BODI underwent multiple Delphi rounds with an international ...
Mattia Congia   +33 more
core   +1 more source

Budd-chiari syndrome and renal arterial neurysms due to behcet disease: a rare association

open access: yesThe Pan African Medical Journal, 2015
Behcet's disease is a multisystemic vasculitis of unknown etiology with a chronic relapsing course. Vasculitis in Behcet's disease with predominant vascular involvement is the only vasculitis that affects both arteries and veins of any size.
Abdussamet Batur   +3 more
doaj   +1 more source

Concurrent presence of buccal mucosal and ophthalmologic lesions in Behcet’s syndrome

open access: yesCaspian Journal of Internal Medicine, 2018
Background: Behcet’s syndrome is a disease with different aspects in its clinical manifestations. The purpose of this study was to evaluate the simultaneous presence of oral mucosal and ophthalmologic lesions in patients with Behcet’s syndrome.
Mojtaba Mikaniki   +4 more
doaj  

Lenalidomide: An Alternative Treatment for Refractory Behçet’s Disease and Relapsing Polychondritis [PDF]

open access: yes, 2019
Introduction: Behçet’s disease (BD) is a chronic systemic condition characterized by recurrent oral and genital ulcers, neurological and vascular manifestations, ocular and skin lesions, and a positive pathergy test.
Brazão, SG   +5 more
core   +1 more source

A case of Hughes–Stovin syndrome (incomplete Behçet’s disease) with extensive arterial involvement:Unmasking the true face of a rare syndrome [PDF]

open access: yes, 2019
Hughes–Stovin syndrome (HSS), characterized by the combination of multiple pulmonary artery aneurysms and deep vein thrombosis, is a rare and an under-recognized clinical entity with less than 40 published cases in English medical literature.
Abd-Elhalim, A.   +7 more
core   +1 more source

Baseline characteristics of the 131 patients with Behçet’s disease.

open access: yes, 2018
Baseline characteristics of the 131 patients with Behçet’s disease.
Hyoung Jun Koh (4217842)   +2 more
core   +1 more source

Tuberculosis Masquerading as Behcet's Disease‐Pseudo Bechet's Syndrome: A Case‐Based Review of Literature

open access: yesRespirology Case Reports
Behcet's disease is a chronic, multisystem variable vessel vasculitis characterised by recurrent oral and genital ulcers, ocular inflammation and a wide range of systemic manifestations.
Rinoosha Rachel   +4 more
doaj   +1 more source

A rare cranial disease: Prolactinoma-associated moyamoya syndrome [PDF]

open access: yes
Moyamoya disease is a rare chronic progressive cerebrovascular disease. The etiology of moyamoya disease has not been established yet. If an underlying cause is detected, moyamoya disease is called moyamoya syndrome.
Meryem Can   +3 more
core   +1 more source

New and future perspectives in Behçet's syndrome

open access: yesThe Turkish Journal of Gastroenterology
Behçet's syndrome is a variable vessel vasculitis characterized by a diverse range of clinical manifestations resulting from inflammation involving several organs and systems.
Bercemhan Sulu, Gulen Hatemi
doaj  

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