- Plasma Cell Myeloma in a Patient with Chronic Myelogenous Leukemia
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Lee JH, Kim YK
- KMID: 2363008
- Lab Med Online.
- 2017 Jan;7(1):49-51.
- doi: 10.3343/lmo.2017.7.1.49
No abstract available. -
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- Guidelines for the Performance Evaluation of In-Vitro Diagnostic Test for the Detection of Norovirus Infection in Korea
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Kim J, Kim HS, Lee S, Oh SH, Woo KS, Kim SY, Min EK
- KMID: 2362999
- Lab Med Online.
- 2017 Jan;7(1):1-6.
- doi: 10.3343/lmo.2017.7.1.1
Norovirus is a leading cause of epidemic and sporadic acute gastroenteritis worldwide. Rapid and accurate detection of norovirus is essential for the prevention and control of norovirus outbreaks. The purpose... -
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- Eosinophilic Meningitis after Bovine Graft Duraplasty for Arnold-Chiari Malformation Type 1 in a 33-year-old Man
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Lee HT, Park PW, Seo YH, Kim KH, Seo JY, Jeong JH, Kim MJ, Ahn JY
- KMID: 2363004
- Lab Med Online.
- 2017 Jan;7(1):34-36.
- doi: 10.3343/lmo.2017.7.1.34
Cases of pediatric eosinophilic meningitis following duraplasty with a bovine graft have been reported. These patients recovered following the surgical removal of the dural graft or steroid therapy. Decompression for... -
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- A Korean Patient with Early Juvenile Form of Metachromatic Leukodystrophy: Biochemical and Molecular Genetic Investigation
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Kim YB, Park HD, Choi R, Lee SY, Ki CS, Song J, Kim JW, Lee J
- KMID: 2363006
- Lab Med Online.
- 2017 Jan;7(1):41-44.
- doi: 10.3343/lmo.2017.7.1.41
Metachromatic leukodystrophy is an inherited lysosomal storage disorder caused by the deficiency of arylsulfatase A activity. The patient in this study, a 5-yr-old girl, presented with progressive psychomotor regression. An... -
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- Prognostic Implications of Elevated Cardiac Troponin T in Patients with Acute Ischemic Stroke
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Jung CL, Jeong TD, Hong KS
- KMID: 2363003
- Lab Med Online.
- 2017 Jan;7(1):28-33.
- doi: 10.3343/lmo.2017.7.1.28
BACKGROUND: Elevated cardiac troponin T (cTnT) levels have been reported in patients with acute ischemic stroke, however, the prognostic relevance is not well established. We evaluated the association between cTnT... -
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- Case of Bile Canalicular Antibody in a Korean Patient with Alcoholic Hepatitis
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Kim SH, Jearn LH, Kim TY, Choi HS
- KMID: 2363005
- Lab Med Online.
- 2017 Jan;7(1):37-40.
- doi: 10.3343/lmo.2017.7.1.37
Bile canalicular antibody (BCA) was first reported in 1969. Many studies of BCA were performed in the 1970s and 1980s and revealed that BCA has a highly positive rate in... -
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- Performance Evaluation of Cartridge-Type Blood Gas Analyzer: i-Smart 300
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Yi A, Kim H, Moon HW, Hur M, Yun YM
- KMID: 2363002
- Lab Med Online.
- 2017 Jan;7(1):20-27.
- doi: 10.3343/lmo.2017.7.1.20
BACKGROUND: Blood gas analysis plays a crucial role in critical care settings, and immediate and precise analysis improves clinical outcomes through prompt treatment. We evaluated the performance of a cartridge-type... -
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- The Usefulness of Hematological Parameters for Assessing Disease Progression in Patients with HIV Infection
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Kim HJ, Park Y, Koo SH, Kwon GC, Kim YS, Sohn KM, Kim J
- KMID: 2363000
- Lab Med Online.
- 2017 Jan;7(1):7-12.
- doi: 10.3343/lmo.2017.7.1.7
BACKGROUND: In patients with HIV, CD4+ T cell count and viral load are the main laboratory tests performed to assess clinical management. However, they require extensive resources. In this study,... -
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- Fragment Analysis for Detection of the FLT3-Internal Tandem Duplication: Comparison with Conventional PCR and Sanger Sequencing
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Lee G, Kim J, Lee S, Jang W, Park J, Chae H, Kim M, Kim Y
- KMID: 2363001
- Lab Med Online.
- 2017 Jan;7(1):13-19.
- doi: 10.3343/lmo.2017.7.1.13
BACKGROUND: We evaluated a sensitive and quantitative method utilizing fragment analysis of the fms-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD), simultaneously measuring mutant allele burden and length, and verified the... -
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- Whole Exome Sequencing in a Korean Child with Joubert Syndrome-related Disorders
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Lee JH, Oh IK, Yoon MJ, Yoon KH
- KMID: 2363007
- Lab Med Online.
- 2017 Jan;7(1):45-48.
- doi: 10.3343/lmo.2017.7.1.45
Joubert syndrome and Joubert syndrome-related disorders (JSRDs) are rare autosomal recessive or X-linked disorders characterized by cerebellar vermis hypoplasia and a brain stem malformation, which presents as the “molar tooth... -
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