- Status of FLT3-ITD Analysis in Korea (2021)
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Kim HY, Kim IS, Kim M, Shin S, Lee JY
- KMID: 2552728
- Lab Med Online.
- 2023 Apr;13(2):72-77.
- doi: 10.47429/lmo.2023.13.2.72
Background: FMS-like tyrosine kinase 3 (FLT3)-internal tandem duplication (ITD) is a crucial prognostic factor in acute myeloid leukemia and a target mutation for FLT3 inhibitor. It is also used for... -
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- Tenosynovitis of the Hand Caused by Kosakonia cowanii After Being Pricked by a Beanstalk
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Yun SY, Kim JR, Hong KH, Yong D, Lee H
- KMID: 2552735
- Lab Med Online.
- 2023 Apr;13(2):114-119.
- doi: 10.47429/lmo.2023.13.2.114
A 77-year-old man with pain in his left hand after being pricked by a beanstalk visited an emergency center. Symptoms and laboratory findings suggested infectious tenosynovitis. Using the Bruker Biotyper... -
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- The First Cases of OPHN1 Exons 1 and 2 Deletion in Two X-linked Intellectual Developmental Disorder Patients in Korea
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Kim KB, Lee S, Kim DH
- KMID: 2552736
- Lab Med Online.
- 2023 Apr;13(2):120-123.
- doi: 10.47429/lmo.2023.13.2.120
OPHN1is located in Xq12 and acts as a regulator for the development of neural tissues in a fetus. Various spectrums of X-linked intellectual disabilities (XLIDs) can occur due to a... -
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- An Algorithm to Work-up ABO Subgroups Presenting as Weak B in a Real-world Laboratory: A Case with a Weak B Phenotype Harboring B101/O04-variant Alleles
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Jeon SJ, Park JH, Shin MG, Park C, Won EJ, Park G
- KMID: 2552733
- Lab Med Online.
- 2023 Apr;13(2):103-108.
- doi: 10.47429/lmo.2023.13.2.103
Weaker ABO subgroups are the main cause of ABO discrepancies, and ABO genotyping studies are crucial to identify them. We performed ABO genotyping to determine the cause of a weak... -
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- Various ABO Genotyping-phenotyping Results for ABO Blood Group Discrepancy: A Retrospective Study
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Lee SJ, Chae S, Yoo J, Jekarl DW, Lee S, Kim M, Kim Y
- KMID: 2552732
- Lab Med Online.
- 2023 Apr;13(2):97-102.
- doi: 10.47429/lmo.2023.13.2.97
The ABO system remains the most important blood group classification system in transfusion medicine. ABO serology testing requires both forward and reverse typing as each grouping result validates the other,... -
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- A Case of T-Lymphoblastic Leukemia with Submicroscopic 1p33 Deletion Resulting in STIL-TAL1 Fusion
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Chang SH
- KMID: 2552734
- Lab Med Online.
- 2023 Apr;13(2):109-113.
- doi: 10.47429/lmo.2023.13.2.109
T-lymphoblastic leukemia (T-ALL) is an aggressive hematologic malignancy associated with poor outcomes. The genetic background of T-ALL is widely heterogeneous and the TAL1 gene is overexpressed in approximately half of... -
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- Current Status and Perspectives for in vitro Medical Devices for Infectious Disease Diagnosis - Survey of Product Development and Clinical Trials
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Kim S, Lee S, Kim S
- KMID: 2552727
- Lab Med Online.
- 2023 Apr;13(2):65-71.
- doi: 10.47429/lmo.2023.13.2.65
Background: The in vitro diagnostic (IVD) medical device industry has experienced remarkable growth during the COVID-19 pandemic. We here survey the existing difficulties in addressing various processes, including IVD development,... -
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- Analysis of Positive Patterns and Follow-up Results of the QuantiFERON-TB Gold-Plus Test in the Screening of Patients and Healthcare Workers
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Shin E, Seo JD, Kim H, Hur M, Yun YM, Moon HW
- KMID: 2552730
- Lab Med Online.
- 2023 Apr;13(2):85-90.
- doi: 10.47429/lmo.2023.13.2.85
Background: The early detection of latent tuberculosis infection is essential for reducing the incidence of tuberculosis (TB). The QuantiFERONTB Gold-Plus (QFT-Plus; Qiagen, Germany) detects both CD8+ and CD4+ T-cell-mediated immune... -
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- Performance Evaluation of QMAC-dRAST Using Consecutive Positive Clinical Blood Culture Samples
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Choi H, Kim D, Kwon M, Byun JH, Jin B, Hong KH, Lee H, Yong D
- KMID: 2552729
- Lab Med Online.
- 2023 Apr;13(2):78-84.
- doi: 10.47429/lmo.2023.13.2.78
Background: Bacteremia is life-threatening to patients, with a case fatality rate of 30–40%. The QMAC-dRAST system (QuantaMatrix, Republic of Korea), which is based on time-lapse imaging technology, can generate antimicrobial... -
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- Coffin-Siris Syndrome: Genotype-Phenotype Clustering and Novel Variants
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Jang J, Chae SW, Shin HS, Cho SI, Kim B, Lee Js, Kim MJ, Park SS, Seong Mw
- KMID: 2552731
- Lab Med Online.
- 2023 Apr;13(2):91-96.
- doi: 10.47429/lmo.2023.13.2.91
Background: Coffin-Siris syndrome (CSS) is a rare disease characterized by features such as developmental delay, intellectual disability, unique facial feature, hypoplasia of the fifth finger or toe, hypertrichosis, and sparse... -
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