Genetic basis of multidrug-resistant Acinetobacter baumannii clinical isolates from three university hospitals in Chungcheong Province, Korea [0.03%]
韩国忠清道三家大学医院临床分离的多重耐药产酸不动杆菌的遗传基础
Sun Hoe Koo,Kye Chul Kwon,Hye Hyun Cho et al.
Sun Hoe Koo et al.
Background: The emergence of multidrug-resistant (MDR) Acinetobacter baumannii as an important opportunistic pathogen has given rise to significant therapeutic challenges in the treatment of nosocomial infections. In the ...
Investigation of toxin gene diversity, molecular epidemiology, and antimicrobial resistance of Clostridium difficile isolated from 12 hospitals in South Korea [0.03%]
韩国12家医院分离的产毒基因多样性、分子流行病学及耐药性研究
Heejung Kim,Seok Hoon Jeong,Kyoung Ho Roh et al.
Heejung Kim et al.
Background: Clostridium difficile is a major cause of antibiotic-associated diarrhea. The objective of this study was to characterize clinical isolates of C. difficile obtained from various regions in Korea with regard to...
Decline in erythromycin resistance in group A Streptococci from acute pharyngitis due to changes in the emm Genotypes rather than restriction of antibiotic use [0.03%]
由于emm基因型的变化而非限制抗生素使用急性咽炎组A链球菌对红霉素耐药性的降低
Eunha Koh,Sunjoo Kim
Eunha Koh
Background: Group A streptococcus (GAS) is the most common cause of bacterial pharyngitis in children. Antibiotic resistance rates and emm genotypes of GAS isolated from patients with acute pharyngitis were studied in 200...
Determination of carbohydrate-deficient transferrin levels by using capillary electrophoresis in a Korean population [0.03%]
应用毛细管电泳法测定韩国人群中碳水化合物缺乏的转铁蛋白水平
Hee-Won Moon,Yeo-Min Yun,Serim Kim et al.
Hee-Won Moon et al.
Background: Carbohydrate-deficient transferrin (CDT) levels have rarely been determined in an Asian population. We evaluated the analytical performance of a test for measuring CDT levels by using capillary electrophoresis...
JAK2 V617F and MPL W515L/K mutations in Korean patients with essential thrombocythemia [0.03%]
JAK2 V617F和MPL W515L/K突变在韩国原发性血小板增多症患者中的研究
Hee-Jung Kim,Ja-Hyun Jang,Eun-Hyung Yoo et al.
Hee-Jung Kim et al.
JAK2 V617F and MPL W515L/K mutations have been reported in approximately 50% and 5% of the patients with essential thrombocythemia (ET), respectively. We investigated the frequency of MPL W515L/K mutations in a series of consecutive patient...
Level of HOXA5 hypermethylation in acute myeloid leukemia is associated with short-term outcome [0.03%]
HOXA5甲基化程度与急性髓系白血病短期预后的关联性研究
Shine Young Kim,Sang-Hyun Hwang,Eun Joo Song et al.
Shine Young Kim et al.
Hypermethylation of the homeobox (HOX) gene promoter leads to decreased expression of the gene during tumor development and is thought to be correlated with the clinical outcome in leukemia. In this study, we performed pyrosequencing to qua...
Determination of the prevalence of aspirin and clopidogrel resistances in patients with coronary artery disease by using various platelet-function tests [0.03%]
应用多种血小板功能试验测定冠心病患者阿司匹林和氯吡格雷抵抗的流行率
Kwang-Sook Woo,Bo-Ram Kim,Ji-Eun Kim et al.
Kwang-Sook Woo et al.
Background: Dual therapy with aspirin and clopidogrel has emerged as the gold standard therapy for patients treated with drug-eluting stents (DES). However, there is variability in patients' responses to this antiplatelet...
Immature platelet fraction: establishment of a reference interval and diagnostic measure for thrombocytopenia [0.03%]
不成熟血小板分数：正常参考区间及诊断血小板减少症的指标建立
Haiyoung Jung,Hee-Kyung Jeon,Hee-Jin Kim et al.
Haiyoung Jung et al.
Background: Immature platelet fraction (IPF, %) is a measure of reticulated platelets (RPs), which represents the state of thrombopoiesis. The IPF is obtained from an automated hematology analyzer as one of the platelet p...
[Proposal of laboratory test panel based on patients' chief complaints in emergency department] [0.03%]
[基于急诊患者主诉的实验室检验项目设置方案探讨]
Hyun Chul Lee,Yu Kyung Kim,Jung Hup Song et al.
Hyun Chul Lee et al.
Background: A test panel is a group of tests that are simultaneously performed for diagnosis and follow-up of patients. Organ-specific or disease-specific test panels are currently available. Since the patient's chief com...
[A case of pseudoisodicentric chromosome 18q detected at prenatal diagnosis] [0.03%]
[产前诊断到的一例18q假等臂染色体病例报告]
Sun Young Cho,Gayoung Lim,So Young Kim et al.
Sun Young Cho et al.
Although trisomy 18 (Edwards' syndrome) or the terminal deletion syndromes of 18p and 18q have been occasionally detected, pseudoisodicentric chromosome 18 is a very rare constitutional chromosomal abnormality. We describe a case of pseudoi...