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Bibliometric and Altmetric Analyses of Publication Activity in the Field of Behcet's Disease in 2010–2019

Kocyigit BF, Akyol A

Background: Behcet's disease (BD) is a systemic vasculitis accompanied by oral-genital ulcers, ocular, cerebral, and gastrointestinal disorders. The aim of this study was to evaluate BD articles published between 2010–2019...
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Anti-Tumor Necrosis Factor Therapy in Intestinal Behçet's Disease

Park J, Cheon JH

Intestinal Behçet's disease is a rare, immune-mediated chronic intestinal inflammatory disease; therefore, clinical trials to optimize the management and treatment of patients are scarce. Moreover, intestinal Behçet's disease is difficult...
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Behcet's Disease Associated with Deep Vein Thrombosis: A Case Report

Ahn HJ, Shin EJ, Gwak MJ, Jeong KH, Lee MH

  • KMID: 2436705
  • Korean J Dermatol.
  • 2018 Jun;56(5):325-328.
Behcet's disease is a multisystem inflammatory disorder with a chronic relapsing course. It is considered a nonspecific systemic vasculitis involving both, venous and arterial circulation. Although lower extremity vein thrombosis...
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Non-sexually Related Genital Ulcer in a 16-year-old Girl (Lipschutz Ulcer)

Soh BW, Lee ES

  • KMID: 2369699
  • Korean J Dermatol.
  • 2017 Jan;55(1):73-74.
No abstract available.
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A Case of Lacrimal Gland MALT Lymphoma in a Patient with Primary Sjögren's Syndrome

Kim HW, Sung YM, Baik JS, Yang SW

PURPOSE: To report a case of lacrimal gland mucosa-associated lymphoid tissue (MALT) lymphoma in a patient with primary Sjögren's syndrome and Behcet's disease. CASE SUMMARY: A 49-year-old female patient with primary...
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Recurrent onycholysis in a patient with Behcet's disease

Kim HS, Lee DS, Lee SH, Kwon WH, Kim YJ

Onycholysis is defined as a distal or distal lateral separation of the nail plate from the underlying or lateral supporting structures including nail bed, hyponychium, and lateral nail fold. Trauma,...
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Genetic Associations of Mitochondrial DNA Polymorphisms with Behcet's Disease in a Korean Population: A Pilot Study

Kwon MH, Joung CI

OBJECTIVE: Pathogenesis of Behcet's disease (BD) is known to be multifactorial and accumulating data suggest genetic mechanisms. Variations in nuclear DNAs have been largely investigated, while studies on mitochondrial DNAs...
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Behcet's Disease Current Activity Form as a Patient's Derived Measure

Choi HJ, Seo MR, Ryu HJ, Baek HJ

OBJECTIVE: This study measured the reliability of the Behcet's Disease Current Activity Form (BDCAF) questionnaire used as a patient self-report form. METHODS: A study was conducted among 63 patients with Behcet's...
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Intestinal Behcet's Disease: A True Inflammatory Bowel Disease or Merely an Intestinal Complication of Systemic Vasculitis?

Kim DH, Cheon JH

Behcet's disease (BD) is a multi-systemic inflammatory disorder of an unknown etiology and shows a chronic recurrent clinical course. When the disease involves the alimentary tract, it is called intestinal...
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Evaluation of Arterial Stiffness in Patients with Behçet's Disease by Using Noninvasive Radiological Methods such as Intima-Media Thickness of the Carotid, Ankle-Brachial Pressure Index, Coronary Artery Calcium Scoring, and Their Relation to Serum Fetuin-A Levels: A Case-Control Study

Uyar B, Solak A, Genc B, Akyildiz M, Sahin N, Uyar IS, Saklamaz A

BACKGROUND: Behcet's disease (BD) is a chronic, recurrent inflammatory systemic vasculitis. Evidence for increased atherosclerosis in BD has been observed. The relation between cardiovascular risk factors and increased atherosclerosis in...
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Overlooked Management and Risk Factors for Anemia in Patients with Intestinal Behcet's Disease in Actual Clinical Practice

Kim B, Park SJ, Hong SP, Cheon JH, Kim TI, Kim WH

BACKGROUND/AIMS: Anemia in patients with inflammatory bowel disease significantly affects the quality of life. The aim of this study was to investigate the frequency of and risk factors for anemia...
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Isolated Lenticulostriate Artery Aneurysm Rupture in a Patient with Behcet's Disease

Hwang S, Chang SH, Chung SW, Ha YJ, Kang EH, Song YW, Lee YJ

Behcet's disease (BD) is characterized by recurrent oro-genital ulcers, skin lesions, and intraocular inflammation, but can also affect various internal organs. Vascular BD usually presents with luminal stenosis, thrombosis, or...
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Cross-cultural adaptation and validation of the Behcet's Disease Current Activity Form in Korea

Choi HJ, Seo MR, Ryu HJ, Baek HJ

BACKGROUND/AIMS: This study was undertaken to perform a cross-cultural adaptation of the Behcet's Disease Current Activity Form (BDCAF, version 2006) questionnaire to the Korean language and to evaluate its reliability...
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Neuro-Behcet's Disease Presenting as Hypertrophic Pachymeningitis

Yoon BN, Kim SJ, Lim MJ, Han JY, Lee KW, Sung JJ, Ha CK, Choi SH

A 25-year-old man presented with blurred vision and chronic headache. His brain MRI revealed bilateral frontal pachymeningeal enhancement with leptomeningeal enhancement. The patient had experienced recurrent oral ulcer and had...
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A Case of Guillain-Barre Syndrome in a Patient of Behcet's Disease

Yoo J, Kim NM, Sung W, Myeong JC, Yun SA, Lee DK, Lim MK, Sheen DH

Behcet's disease (BD) is a multi-systemic inflammatory disease of unknown origin that affects nearly all organs including the nervous system. Although the neurological involvement is less frequent than other major...
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A Case of Azathioprine Induced Warfarin Resistance in Behcet's Disease

Kim SR, Leem DW, Moon IJ, Koh BS, Chang MH, Yoo J, Yang HC, Lee CH

Behcet's disease is characterized by recurrent oral aphthous ulcers, genital ulcers, uveitis, and skin lesions. Thrombosis associated with vascular inflammation in patients with Behcet's disease presents various clinical symptoms. Warfarin...
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Clinical Experience of Interferon Alfa-2a Treatment for Refractory Uveitis in Behcet's Disease

Park JY, Chung YR, Lee K, Song JH, Lee ES

Behcet's disease (BD) involves multisystem vasculitis of unknown origin. Ocular manifestations of BD mostly include bilateral panuveitis and retinal vasculitis, which are very challenging to treat. Interferon alfa-2a (IFN) has...
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Carpal Tunnel Syndrome in Behcet's Disease

Lee J, Cho S, Kim DY, Zheng Z, Park H, Bang D

PURPOSE: Behcet's disease (BD) is a chronic inflammatory disease characterized by orogenital ulcers, skin and ocular lesions, in addition to articular, vascular, and neurologic symptoms. Carpal tunnel syndrome (CTS), can...
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mRNA Expression Level of Interleukin Genes in the Determining Phases of Behcet's Disease

Taheri S, Borlu M, Evereklioglu C, Ozdemir SY, Ozkul Y

BACKGROUND: Behcet's disease (BD), first described in 1937 as a triadic complex of symptoms (oral aphthae, genital ulcers, and hypopyon uveitis), is a chronic, relapsing, multisystemic idiopathic inflammatory disease. OBJECTIVE: The...
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Fregoli Syndrome Due to Right Hippocampal Vasculitis in Neuro-Behcet's Disease

Seo JY, Kim TW, You AY, Shin BS

  • KMID: 1775112
  • J Korean Neurol Assoc.
  • 2015 Feb;33(1):40-43.
We report a 40-year-old man with known neuro-Behcet's disease who showed Fregoli syndrome after a seizure attack. A patient with Fregoli syndrome strongly believes that the psychological identity of a...
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