Results 111 to 120 of about 4,852,104 (194)

Demographical and clinical characteristics of patients with Behcet’s disease and normal individuals.

, 2016
Demographical and clinical characteristics of patients with Behcet’s disease and normal individuals.
Kenji Takai (2623126), Jun Shimizu (548113), Takao Kubota (2623132), Yuji Ueda (2623117), Sueshige Wakisaka (2623123), Tomoko Suzuki (206765), Noboru Suzuki (230750), Erika Takada (2623135), Nagisa Arimitsu (2623120), Naruyoshi Fujiwara (2623129)   +9 more
core   +1 more source

Acute Fulminant Systemic Granulocytic Vasculitis Involving Arteries and Veins in Vacuoles, E1 Enzyme, X‐Linked, Autoinflammatory, Somatic (VEXAS) Syndrome: An Autopsy Case Report

Pathology International, Volume 76, Issue 9, September 2026.
We report an autopsy case of VEXAS syndrome presenting with aggressive clinical course. Pathologically, the disease manifested as systemic granulocytic vasculitis affecting both arteries and veins, characterized by the presence of histiocytoid myeloid cells associated with low‐risk MDS.
Kayo Ueda, Masakazu Fujimoto, Yumi Shiroishi, Masafumi Ito, Masahiko Osawa, Mayumi Inaba   +5 more
wiley   +1 more source

The Effect of Caregiver Burden on Healthy Lifestyle Behaviours of People Caring for Patients With Alzheimer's Disease: A Cross‐Sectional Study

Scandinavian Journal of Caring Sciences, Volume 40, Issue 3, September 2026.
ABSTRACT Objectives This study aimed to determine the effects of caregiver burden on the healthy lifestyle behaviours of people caring for patients with Alzheimer's disease. Methods The Caregiver Burden Inventory (CBI) and the Healthy Lifestyle Behaviour Scale‐II (HLBS‐II) were administered to caregivers of Alzheimer's disease patients who were ...
Büşra Neva Tekin, Sıdıka Kaya, Nigar Esra Erkoç Ataoğlu, Mesut Teleş   +3 more
wiley   +1 more source

Mediterranean Fever Gene Mutations in Greek Patients with Behcet’s Disease

, 2012
Objective: It is known that clinical similarities between Behcet’s disease and Familial Mediterranean Fever have led to the hypothesis of a common pathogenesis. Familial Mediterranean Fever is caused by MEFV gene mutations coding for pyrin.
. K Konstantopoulos, E Kanta, V Papadopoulos, P Kaklamanis, M Hatzinikolaou, V Kalotychou,
core  

Fever, Leukocytosis, and Ulcerated Vulvar Lesions: An Atypical Presentation Concerning Behcet’s Disease

Behcet’s disease (BD) is a variable-vessel vasculitis commonly presenting in early adulthood with painful oral aphthous ulcers, genital ulcers, uveitis, pathergy, and skin lesions.
Anders, Casey, Pearce, Brenden, Collier, Victor, Patrick Eisenberg, Austin   +3 more
core   +1 more source

Surgery for pseudoaneurysm following the Bentall procedure in a patient with Behçet’s disease: A case report

Journal of International Medical Research
Behçet’s disease, also known as the oral–ocular–genital syndrome, is a chronic systemic vasculitis characterized by recurrent oral and genital ulcers as well as ocular manifestations such as uveitis and conjunctivitis.
Dou Yuan
doaj   +1 more source

A Changed Man: A Rare Case of Behcet’s Disease Autoimmune Encephalitis

Behcet’s disease (BD) is characterized by recurrent oral ulcers with concomitant systemic multi-organ involvement, which may include neurological disease, ocular disease, vascular disease, genital ulcers, skin lesions, and arthritis.
London, Jonathan, Tharayil, Zubin, Rulka, Kevin, Joseph, Justeena, Bobba, Gayatri, Gudesblatt, Mark   +5 more
core   +1 more source

TWO CASES COMBINED WITH BEHCET’S DISEASE AND RHEUMATIC VALVULAR HEART DISEASE WERE DIAGNOSED

Eurasian Journal of Medicine, 2019
Recent studies have revealed that streptococci play an important role in the etiology of Behcet's disease. As it is known, rheumatic valvular heart disease results from carditis occuring after group A streptococcal infections.
Engin Bozkurt, Şakir Arslan, Refik Ali Sarı   +2 more
doaj  

Behcet’s disease with recurrent thoracic aortic aneurysm combined with femoral artery aneurysm: a case report and literature review

, 2017
Background Aneurysm or pseudoaneurysm is the main vascular complication of Behcet’s disease. Most hospitals adopt endovascular treatment. Case presentation We report a case of Behcet’s disease with recurrent thoracic aortic aneurysm combined with femoral
Shi-Huai Zhang, Fu-Xian Zhang
core   +1 more source

Single-cell RNA sequencing of intestinal Behçet’s disease identifies putative pathogenic programs and potential therapeutic targets

Biomolecules & Biomedicine
Intestinal Behçet’s disease is a rare, refractory subtype of systemic vasculitis, characterized by deep ileocecal ulcers and extensive clinical overlap with Crohn’s disease, while the cellular and molecular mechanisms underlying its pathogenesis remain ...
Chengzhen Lyu, Kun He, Shuai Li, Ziqi Guo, Xiaxiao Yan, Rou Tang, Yanan Shi, Jianyekai Tuerheng, Weiyang Zheng, Lingjuan Jiang, Yi Hu, Dong Wu   +11 more
doaj   +1 more source