Results 71 to 80 of about 1,238,132 (184)
Interferon Induced Focal Segmental Glomerulosclerosis
Case Reports in Nephrology, 2016 Behçet’s disease is an inflammatory disease of unknown etiology which involves recurring oral and genital aphthous ulcers and ocular lesions as well as articular, vascular, and nervous system involvement.
Yusuf Kayar +7 more
doaj +1 more source
Neutrophils: Heterogeneity, Biology, Diseases, and Therapeutic Strategies
MedComm, Volume 7, Issue 11, November 2026.Neutrophils exhibit remarkable functional plasticity and play dual roles in tissue protection and disease progression. This review summarizes their key biological functions and highlights the shift from conventional broad‐spectrum interventions to neutrophil‐based drug delivery systems.
Yibing Zhang +4 more
wiley +1 more source
, 2015 Identification of 123 metabolites from synovial fluid samples of 24 patients with Behcet’s disease with arthritis and seronegative arthritis using BinBase.
Jiwon Hwang (571261) +5 more
core +1 more source
Behçet’s Disease and Intracardiac Thrombosis: A Report of Three Cases
Case Reports in Rheumatology, 2013 We present three patients with Behçet’s disease associated with intracardiac thrombus and pulmonary vascular involvement. One of these patients had also Budd-Chiari syndrome.
Nurşen Düzgün +8 more
doaj +1 more source
Science Education, Volume 110, Issue 6, Page 1673-1692, November 2026.ABSTRACT Science identity is often conceptualized through constructs such as performance, competence, recognition, and interest, with prior research highlighting the roles of race, gender, and cultural background in shaping students' experiences. However, limited scholarship has examined how disability interacts with science identity in postsecondary ...
Ariel Chasen, Maura Borrego
wiley +1 more source
Demographical details, underlying diseases, and diagnostic procedures of the patients.
, 2015 * Vasculitis: Behcet’s disease, microscopic polyangiitis, granulomatosis with polyangiitis** Other CTDs: Sjogren syndrome (SS), undifferentiated connective tissue disease (UCTD), mixed connective tissue disease, scleroderma# Immunosuppressive agents ...
Kai-Feng Xu (305907) +6 more
core +1 more source
Bilateral Hemophthalmus — the First Symptom of Behcet’s Disease (Clinical Case) [PDF]
, 2016 Behcet’s disease (BD) — a systemic chronic idiopathic inflammatory recurrent disease of unknown etiology. The development of the disease involve a combination of various factors, among them the most important is genetic and infectious.
E. N. Panina +5 more
core +1 more source
Millard–Gubler Syndrome due to Parenchymal Neuro-Behcet’s Syndrome Lesion: A Rare Case Report
Acta Neurologica TaiwanicaBehcet's disease; it is a vascular-inflammatory chronic recurrent disease that can affect many systems in the body. Millard–Gubler syndrome is one of the brainstem syndromes that occur due to lesions involving the ventral part of the caudal pons.
Bünyamin Tosunoğlu +3 more
doaj +1 more source
, 2000 Adamantiades-Behcet’s disease is a multisystem recurrent syndrome with vasculitis being the underlying histopathological lesion. We report on a patient with Behcet’s disease who developed a renal mass raising the suspicion of a malignant neoplasm, The ...
Korovesis, K +5 more
core
Budd-chiari syndrome and renal arterial neurysms due to behcet disease: a rare association
The 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