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Can Calprotectin Show Subclinical Inflammation in Familial Mediterranean Fever Patients?

Asan G, Derin ME, DoÄŸan HO, Bayram M, Åžahin M, Åžahin A

BACKGROUND: Familial Mediterranean fever (FMF) is an autoinflammatory disease that has self-limiting inflammatory attacks during polyserositis. Hepcidin is a protein, and interleukin-6 stimulation increases hepcidin levels. Calprotectin (CLP) is a...
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Primary Localized Amyloidosis in Extraocular Muscles

Han SH, Kim YD, Woo KI

PURPOSE: Primary localized amyloidosis is a disease characterized by the deposition of abnormal protein fibrils in a specific tissue without systemic involvement. We report a rare case of primary amyloidosis...
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Primary Amyloidosis Localized to the Conjunctiva

Noh HJ, Park BC, Koh JW

PURPOSE: To report a case of primary amyloidosis localized to the conjunctiva. CASE SUMMARY: A 19-year-old male with a conjunctival mass and foreign body sensations in the right eye transferred from...
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A Stepwise Diagnostic Approach to Cystic Lung Diseases for Radiologists

Lee KC, Kang EY, Yong HS, Kim C, Lee KY, Hwang SH, Oh YW

Lung cysts are commonly seen on computed tomography (CT), and cystic lung diseases show a wide disease spectrum. Thus, correct diagnosis of cystic lung diseases is a challenge for radiologists....
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A Case of Basal Cell Carcinoma with a Unique Pattern of Plasma Cell Infiltration

Choi W, Hahn HJ, Myung KB, Cheong SH

  • KMID: 2454373
  • Korean J Dermatol.
  • 2019 Jul;57(6):324-327.
Basal cell carcinoma (BCC) is the most common malignant skin tumor that usually develops in the head and neck region. It has a wide range of histological variants and constitutes...
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Recent Update of Advanced Imaging for Diagnosis of Cardiac Sarcoidosis: Based on the Findings of Cardiac Magnetic Resonance Imaging and Positron Emission Tomography

Chang S, Lee WW, Chun EJ

Sarcoidosis is a multisystem disease characterized by noncaseating granulomas. Cardiac involvement is known to have poor prognosis because it can manifest as a serious condition such as the conduction abnormality,...
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Renal tubular P-glycoprotein expression is reduced in plasma cell disorders

Heybeli C, Oktan MA, Arda HU, Yildiz S, Unlu M, Cavdar C, Sifil A, Celik A, Sarioglu S, Camsari T

BACKGROUND: P-glycoprotein (P-gp) transports many chemicals that vary greatly in their structure and function. It is normally expressed in renal proximal tubular cells. We hypothesized that P-gp expression influences light...
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Tafamidis, a Noninvasive Therapy for Delaying Transthyretin Familial Amyloid Polyneuropathy: Systematic Review and Meta-Analysis

Zhao Y, Xin Y, Song Z, He Z, Hu W

BACKGROUND AND PURPOSE: Tafamidis functions to delay the loss of function in transthyretin familial amyloid polyneuropathy (TTR-FAP), which is a rare inherited amyloidosis with progressive sensorimotor and autonomic polyneuropathy. This...
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Contemporary Imaging Diagnosis of Cardiac Amyloidosis

Lee SP, Park JB, Kim HK, Kim YJ, Grogan M, Sohn DW

Cardiac amyloidosis is a rare disease that frequently presents as ventricular hypertrophy. However, diagnosis is not always easy or straightforward as there are several myocardial disorders that phenocopy cardiac amyloidosis....
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Pulmonary tuberculosis occurred in patient with Tracheobronchopathia Osteochondroplastica

Shim JW, Kim JH, Jang YW, Sung YM, Kim N, Lee SM

Tracheobronchopathia osteoplastica (TO) is a rare benign disease in which the anterior inner wall of the tracheobronchus changes because of abnormal chondrogenesis or ossification, while the posterior wall of the...
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A Pediatric Case of Inflammatory Bowel Disease with Renal Amyloidosis

Hyun H, Park E, Kim JH, Cho MH, Kang HG, Moon JS, Moon KC, Ha IS, Cheong HI

Amyloidosis is a rare disease that results from the deposition of extracellular protein in various body tissues, causing progressive organ dysfunction. Secondary renal amyloidosis is a rare but serious complication...
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Characteristics of South Korean Patients with Hereditary Transthyretin Amyloidosis

Choi K, Seok JM, Kim BJ, Choi YC, Shin HY, Sunwoo IN, Kim DS, Sung JJ, Lee GY, Jeon ES, Kim NH, Min JH, Oh J

BACKGROUND AND PURPOSE: This retrospective cross-sectional study included 18 patients from unrelated families harboring mutations of the transthyretin gene (TTR), and analyzed their characteristics and geographical distribution in South Korea. METHODS:...
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A Case of Amyloidosis Presenting as Lymphadenopathy at the Porta Hepatis

Lee JI, Kim JS, Kim BW

We report a rare case of systemic amyloidosis with gastrointestinal and lymph node involvement. A 64-year-old woman was admitted to our hospital with dyspepsia and weight loss. Initial esophagogastroduodenoscopy (EGD)...
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Duodenal Amyloidosis

Yoon HJ, Shin SY, Nahm JH, Park H

No abstract available.
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Plasma Oligomeric Beta Amyloid in Alzheimer's Disease with History of Agent Orange Exposure

Yang Y, Giau VV, An SS, Kim S

BACKGROUND AND PURPOSE: During the Vietnam War, many Korean soldiers were exposed to Agent Orange. Until now, there existed only limited evidence of association between exposure to Agent Orange and...
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Asymptomatic Localized Gastric Amyloidosis with Two Separate Lesions

Lim JH, Kim J, Seo JY, Bae JH

Amyloidosis is a disease in which amyloid is abnormally accumulated in the tissue. The kidney and heart are the most commonly involved organs. Gastric involvement is relatively common in systemic...
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Localized Gastric Amyloidosis with Kappa and Lambda Light Chain Co-Expression

Ahn YH, Rhee YY, Choi SC, Seo GS

Esophagogastroduodenoscopy for cancer screening was performed in a 55-year-old woman as part of a health screening program, and revealed a depressed lesion approximately 20 mm in diameter in the lesser...
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Radiologic Manifestation of Intra-Abdominal Involvement of Systemic Amyloidosis Secondary to Renal Cell Carcionma

Lee YJ, Han GJ, Kim S, Lee NK, Shin HJ, Ha HK, Kim TU

Amyloidosis has a wide spectrum of manifestations in numerous abdominal organs. It can be categorized into primary or secondary disease according to the presence of accompanying conditions, such as rheumatoid...
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Unexpected amyloidosis, mimicking a splenic cyst

Chang CF, Liao YS, Chen YG, Ye RH

No abstract available.
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Duodenal amyloidosis secondary to ulcerative colitis

Park SW, Jee SR, Kim JH, Lee SH, Hwang JW, Jang JG, Lee DW, Seol SY

Amyloidosis is defined as the extracellular deposition of non-branching fibrils composed of a variety of serum-protein precursors. Secondary amyloidosis is associated with several chronic inflammatory conditions, such as rheumatologic or...
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