Results 101 to 110 of about 1,238,132 (184)

Severe cardiovascular involvement in Hughes-Stovin syndrome

open access: yes, 2017
Hughes-Stovin syndrome (HSS) is a rare autoimmune vasculitis and is characterized by the simultaneous presence of deep venous thrombosis and pulmonary artery aneurysms.
Konstantin Nikolaou   +6 more
core   +1 more source

The Impact of Coping Strategies in Behcet’s Disease: A Case‑control Study [PDF]

open access: yes, 2020
Background: Behcet’s disease (BD) is a chronic, systemic inflammatory disease characterized with higher prevalence of psychiatric disorders,  particularly major depression.
Atay, I.M., Erturan, I.
core  

Evaluation of IFN-gamma and HSP70 level in the saliva of Behcet’s disease patients with active oral lesions

open access: yes, 2019
Introduction:\ua0Behcet’s disease (BD) is a multi-systemic inflammatory disorder. Evaluating the production of cytokines such as interferon gamma and biomarkers such as heat shock protein-70 (HSP70)is an important way to study the pathogenesis and ...
Bonyadi, Mohammadreza   +15 more
core   +1 more source

Description of the patient subgroups.

open access: yes, 2013
ITM, idiopathic transverse myelitis; OIND, other inflammatory neurological diseases; NS, neurosarcoidosis; PNS, paraneoplastic syndrome; NL, neurolupus; NB, neuro-Behcet’s disease; PACNS, primary angiitis of the central nervous system; NBo ...
Viktoria Kapina (450939)   +7 more
core   +1 more source

Disseminated Tuberculosis During the Course of Behçet's Disease: A Case Report

open access: yesThe Turkish Journal of Gastroenterology, 2012
In this article, a 22 year-old male with disseminated tuberculosis during the course of Behçet's disease who was admitted with the complaints of fever, headache and fatigue was presented. The initial diagnosis was neuro- Behçet's syndrome.
İbak GÖNEN   +8 more
doaj  

Orogenital ulcers and the Behcet’s disease [PDF]

open access: yes
Behcet’s’s disease is a systemic vasculitis involving small to large veins and arteries. It is a sporadic disease, mostly prevalent among the ancestors of the silk route. It is characterized by recurrent oral ulcers, genital ulcers, and uveitis.
Narmada, Vatti   +3 more
core   +1 more source

Analysis on clinical characteristics of chronic progressive parenchymal neuro-Behçet's syndrome

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2019
Objective To summarize the clinical manifestations of chronic progressive parenchymal neuro-Behçet's syndrome (CPPNBS). Methods The diagnosis and treatment of one patient with CPPNBS was reviewed and analyzed. Taking neuro Behçet's syndrome, neuro Behçet'
Cui LU   +6 more
doaj  

Case report: Cerebral sinus vein thrombosis in VEXAS syndrome [PDF]

open access: yes
VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, and somatic) syndrome is a newly described hemato-inflammatory acquired monogenic entity that presents in adulthood. One of the main features of VEXAS syndrome is a high venous thromboembolism (VTE)
Jeremy Molad   +7 more
core   +1 more source

Ibuprofen-induced tubulointerstitial nephritis with Fanconi syndrome in a patient with Behçet’s disease mimicking TINU syndrome: a diagnostic challenge clarified by a structured clinical approach

open access: yesRenal Replacement Therapy
Background The coexistence of tubulointerstitial nephritis (TIN) and uveitis commonly raises suspicion for tubulointerstitial nephritis and uveitis (TINU) syndrome.
Yutaro Hirashima   +6 more
doaj   +1 more source

Coexistence of Behçet's Disease and Ankylosing Spondylitis: A Case Report

open access: yesThe Turkish Journal of Gastroenterology, 2010
Although overlap syndrome is frequently encountered in rheumatology practice, only a few cases of coexisting Behçet's disease and ankylosing spondylitis have been reported in the literature.
Hikmet Koçyiğit   +5 more
doaj  

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