- Infection Control of Dialysis Patients for Coronavirus Infectious Disease-19 Response
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Choi JY, Son HJ, Cha KS, Kim SR, Shin MJ, Choi JR, Han SH
- KMID: 2503756
- Korean J healthc assoc Infect Control Prev.
- 2020 Jun;25(1):11-20.
- doi: 10.14192/kjicp.2020.25.1.11
The effects of coronavirus disease 19 (COVID-19) on patients with chronic kidney disease have not yet been fully studied, but acute kidney damage has been reported in some COVID- 19... -
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- Infection Control during Surgery for Patients with Confirmed or Suspected Coronavirus Disease-19
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Han SH, Kim SR, Cha KS, Son HJ, Shin MJ, Choi JR, Choi JY
- KMID: 2503755
- Korean J healthc assoc Infect Control Prev.
- 2020 Jun;25(1):4-10.
- doi: 10.14192/kjicp.2020.25.1.4
The prevalence of coronavirus disease (COVID-19) has led to an increase in the number of patients being treated at medical institutions, including the number of patients requiring surgical treatments. Although... -
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- Implementing a multidisciplinary care bundle to reduce colon surgical site infections
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Park CM, Ha TS, Lee WY, Chung DR, Park YA, Choi JR, Jeong NY
- KMID: 2508325
- Ann Surg Treat Res.
- 2020 Nov;99(5):285-293.
- doi: 10.4174/astr.2020.99.5.285
Purpose: The aim of this study was to investigate how rates of surgical site infections (SSI) were changed over 2 years after applying colon SSI bundle in patients who underwent... -
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- Clinical Features and Treatment Efficacy in CDKL5 Mutation-Related Epileptic Encephalopathy in the Infant
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Koo CM, Kim SH, Kim HD, Lee JS, Choi JR, Lee ST, Kang HC
- KMID: 2453788
- Ann Child Neurol.
- 2019 Jun;27(2):33-37.
- doi: 10.26815/acn.2019.00052
PURPOSE: Mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene are associated with epileptic encephalopathy and severe cognitive impairment. We aim to characterize the association between this gene and treatment efficacy. METHODS:... -
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- Clinical Features and Treatment Efficacy in CDKL5 Mutation-Related Epileptic Encephalopathy in the Infant
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Koo CM, Kim SH, Kim HD, Lee JS, Choi JR, Lee ST, Kang HC
- KMID: 2452692
- J Korean Child Neurol Soc.
- 2019 Jun;27(2):33-37.
- doi: 10.26815/acn.2019.00052
PURPOSE: Mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene are associated with epileptic encephalopathy and severe cognitive impairment. We aim to characterize the association between this gene and treatment efficacy. METHODS:... -
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- FLT3 Internal Tandem Duplication in Patients With Acute Myeloid Leukemia Is Readily Detectable in a Single Next-Generation Sequencing Assay Using the Pindel Algorithm
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Kim B, Kim S, Lee ST, Min YH, Choi JR
- KMID: 2431612
- Ann Lab Med.
- 2019 May;39(3):327-329.
- doi: 10.3343/alm.2019.39.3.327
No abstract available. -
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- Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
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Bong JB, Kim SW, Lee ST, Choi JR, Shin HY
- KMID: 2449297
- J Korean Neurol Assoc.
- 2019 Feb;37(1):69-72.
- doi: 10.17340/jkna.2019.1.13
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), which is caused by mutations in SACS gene, is a very rare neurodegenerative disorder characterized by the clinical triad of early onset cerebellar... -
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- Development and Evaluation of an Infection Control Education Program for Postpartum Care Workers
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Kim SR, Kim SH, Son HJ, Cho NH, Cha KS, Chun HK, Choi JR, Hong HK
- KMID: 2467905
- Korean J healthc assoc Infect Control Prev.
- 2019 Dec;24(2):60-68.
- doi: 10.14192/kjicp.2019.24.2.60
BACKGROUND: This study was conducted to investigate the educational needs of employees in charge of practical services at postpartum care centers and to test the improvement of infection control-related knowledge... -
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- Radon Exposure-induced Genetic Variations in Lung Cancers among Never Smokers
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Choi JR, Koh SB, Kim HR, Lee H, Kang DR
- KMID: 2416148
- J Korean Med Sci.
- 2018 Jul;33(29):e207.
- doi: 10.3346/jkms.2018.33.e207
BACKGROUND: Lung cancer in never smokers (LCINS) differs etiologically and clinically from lung cancer attributed to smoking. After smoking, radon exposure is the second leading cause and the primary risk... -
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- Serum Fibroblast Growth Factor 21 and New-Onset Metabolic Syndrome: KoGES-ARIRANG Study
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Choi JR, Kim JY, Park IH, Huh JH, Kim KW, Cha SK, Park KS, Sohn JH, Park JT, Koh SB
- KMID: 2418793
- Yonsei Med J.
- 2018 Mar;59(2):287-293.
- doi: 10.3349/ymj.2018.59.2.287
PURPOSE: Fibroblast growth factor 21 (FGF21) is a crucial metabolic regulator, with multiple favorable effects on glucose homeostasis and lipid metabolism. Since serum FGF21 level has been implicated as a... -
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- Erratum: Novel Genetic Associations Between Lung Cancer and Indoor Radon Exposure
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Choi JR, Koh SB, Park SY, Kim HR, Lee H, Kang DR
- KMID: 2416953
- J Cancer Prev.
- 2018 Mar;23(1):61-61.
- doi: 10.15430/JCP.2018.23.1.61
The original version of this article contained error in the name of the fourth author which was given incorrectly as Hye Run Kim. The author’s name should have been written... -
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- Erratum: Novel Genetic Associations Between Lung Cancer and Indoor Radon Exposure
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Choi JR, Koh SB, Park SY, Kim HR, Lee H, Kang DR
- KMID: 2447452
- J Cancer Prev.
- 2018 Dec;23(4):197-197.
- doi: 10.15430/JCP.2018.23.4.197
The original version of the article contained error in the funding statement in Acknowledgements section. -
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- Report on the External Quality Assessment Scheme for Cytogenetics and Molecular Cytogenetics in Korea (2016–2017)
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Kim J, Shin S, Kim B, Lee ST, Kim M, Choi JR
- KMID: 2437187
- J Lab Med Qual Assur.
- 2018 Dec;40(4):188-198.
- doi: 10.15263/jlmqa.2018.40.4.188
In both 2016 and 2017, the cytogenetic and molecular cytogenetic programs conducted three assessments for the Korean Association of External Quality Assessment Service. A total of six cases with chromosomal... -
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- Early Diagnosis of KBG Syndrome Using Diagnostic Exome Sequencing
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Hong JH, Kim SH, Lee ST, Choi JR, Kang HC, Lee JS, Kim HD
- KMID: 2437112
- J Korean Child Neurol Soc.
- 2018 Dec;26(4):272-275.
- doi: 10.26815/jkcns.2018.26.4.272
KBG syndrome is a rare neurodevelopmental disorder characterized by intellectual disability, skeletal anomalies, short stature, craniofacial dysmorphism, and macrodontia. ANKRD11 gene mutation and 16q24.3 microdeletion have been reported to cause... -
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- Implantable Neural Probes for Brain-Machine Interfaces – Current Developments and Future Prospects
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Choi JR, Kim SM, Ryu RH, Kim SP, Sohn JW
- KMID: 2430105
- Exp Neurobiol.
- 2018 Dec;27(6):453-471.
- doi: 10.5607/en.2018.27.6.453
A Brain-Machine interface (BMI) allows for direct communication between the brain and machines. Neural probes for recording neural signals are among the essential components of a BMI system. In this... -
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- A contact investigation after exposure to a child with disseminated tuberculosis mimicking inflammatory bowel disease
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Kim D, Lee S, Kang SH, Park MS, Yoo SY, Jeon TY, Choi JS, Kim B, Choi JR, Cho SY, Chung DR, Choe YH, Kim YJ
- KMID: 2433705
- Korean J Pediatr.
- 2018 Nov;61(11):366-370.
- doi: 10.3345/kjp.2018.07206
PURPOSE: Tuberculosis (TB) is one of the most important diseases that cause significant mortality and morbidity in young children. Data on TB transmission from an infected child are limited. Herein,... -
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- Deletion of 20p13 and Duplication of 20p13p12.3 in a Patient with Delayed Speech and Development
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Kwon SS, Kim J, Shin S, Lee ST, Lee KA, Choi JR
- KMID: 2397609
- Ann Lab Med.
- 2018 Jan;38(1):77-79.
- doi: 10.3343/alm.2018.38.1.77
No abstract available. -
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- Application of Multiplex Ligation-Dependent Probe Amplification Assay for Genotyping Major Blood Group Systems Including DEL Variants in the D-Negative Korean Population
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Kim B, Lee ST, Kim S, Choi JR, Kim HO
- KMID: 2397599
- Ann Lab Med.
- 2018 Jan;38(1):32-38.
- doi: 10.3343/alm.2018.38.1.32
BACKGROUND: The DEL blood type, a very weak D variant, is a major concern in the field of transfusion medicine because of its potential to cause anti-D alloimmunization. We investigated... -
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- Quinidine Trial in a Patient with Epilepsy of Infancy with Migrating Focal Seizure and KCNT1 Mutation
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Jee N, Ko A, Kim SH, Lee JS, Kim HD, Lee ST, Choi JR, Kang HC
- KMID: 2392554
- J Korean Child Neurol Soc.
- 2017 Sep;25(3):169-173.
- doi: 10.26815/jkcns.2017.25.3.169
Epilepsy of infancy with migrating focal seizure (MFEI) is an early-onset epileptic encephalopathy characterized by randomly migrating focal seizures and psychomotor deterioration. It is associated with mutations in a variety... -
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- Detection of Immunoglobulin Heavy Chain Gene Clonality by Next-Generation Sequencing for Minimal Residual Disease Monitoring in B-Lymphoblastic Leukemia
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Shin S, Hwang IS, Kim J, Lee KA, Lee ST, Choi JR
- KMID: 2376791
- Ann Lab Med.
- 2017 Jul;37(4):331-335.
- doi: 10.3343/alm.2017.37.4.331
Minimal residual disease (MRD) following B-lymphoblastic leukemia (B-ALL) treatment has gained prognostic importance. Clonal immunoglobulin heavy chain (IGH) gene rearrangement is a useful follow-up marker in B-ALL owing to its... -
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