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A loss function approach to group preference aggregation in the AHP

Computers & operations research, 2008-03, Vol.35 (3), p.884-892

2008

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A novel variant of the POLR3A gene in a patient with hypomyelinating POLR3-related leukodystrophy

Clinica chimica acta, 2022-08, Vol.533, p.15-21

2022

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Diversity of Clinical and Molecular Characteristics in Korean Patients with 16p11.2 Microdeletion Syndrome

International journal of molecular sciences, 2023-12, Vol.25 (1), p.253

2023

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Isolation of EpCAM+/CD133− hepatic progenitor cells

Molecules and Cells, 2013, 36(5), , pp.424-431

2013

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Identification of a novel U2HR mutation in a Korean woman with Marie Unna hereditary hypotrichosis

International journal of dermatology, 2014-11, Vol.53 (11), p.1358-1361

2014

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Clinical and Genetic Characteristics of Early and Advanced Gastric Cancer

Current issues in molecular biology, 2024-02, Vol.46 (2), p.1208-1218

2024

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Isolation and Genetic Characterization of Orientia tsutsugamushi from Scrub Typhus Patients in Gyeongsangnam-do, Korea

Journal of bacteriology and virology, 2016-12, Vol.46 (4), p.275

2016

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Accuracy Validation of the Elecsys HBsAg II Quant Assay and Its Utility in Resolving Equivocal Qualitative HBsAg Results

Medicina (Kaunas, Lithuania), 2023-02, Vol.59 (3), p.443

2023

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Copy number variation analysis using next-generation sequencing identifies the CFHR3/CFHR1 deletion in atypical hemolytic uremic syndrome: a case report

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.603-608

2022

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A NOVEL C.800G>C VARIANT OF THE ITM2B GENE IN FAMILIAL KOREAN DEMENTIA

IBRO neuroscience reports, 2023-10, Vol.15, p.S498-S498

2023

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Clinical Features and Risk Factors Associated With 30-Day Mortality in Patients With Pneumonia Caused by Hypervirulent Klebsiella pneumoniae (hvKP)

Annals of Laboratory Medicine, 2020, 40(6), , pp.481-487

2020

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The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructure

Orphanet journal of rare diseases, 2022-10, Vol.17 (1), p.1-372, Article 372

2022

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Case Report: Novel Likely Pathogenic ACTN2 Variant Causing Heterogeneous Phenotype in a Korean Family With Left Ventricular Non-compaction

Frontiers in pediatrics, 2021-03, Vol.9, p.609389

2021

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Case report: Compound heterozygosity in PKLR gene with a large exon deletion and a novel rare p.Gly536Asp variant as a cause of severe pyruvate kinase deficiency

Frontiers in pediatrics, 2022-12, Vol.10, p.1022980

2022

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Dermabacter jinjuensis sp. nov., a novel species of the genus Dermabacter isolated from a clinical specimen

International journal of systematic and evolutionary microbiology, 2016-07, Vol.66 (7), p.2573-2577

2016

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Seroprevalence of Neutralizing Antibodies against Japanese Encephalitis Virus among Adolescents and Adults in Korea: A Prospective Multicenter Study

Vaccines (Basel), 2020-06, Vol.8 (2), p.328

2020

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SPA0355 prevents ovariectomy-induced bone loss in mice

The Korean journal of physiology & pharmacology, 2019-01, Vol.23 (1), p.47-54

2019

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A case of torsion of a mucinous cystadenoma in triple-X syndrome with pure gonadal dysgenesis

Archives of gynecology and obstetrics, 2006-06, Vol.274 (3), p.174-177

2006

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Insights into Platelet Storage and the Need for Multiple Approaches

Annals of clinical and laboratory science, 2015, Vol.45 (6), p.713-719

2015

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Paper-based multiplex analytical device for simultaneous detection of Clostridioides difficile toxins and glutamate dehydrogenase

Biosensors & bioelectronics, 2021-03, Vol.176, p.112894-112894, Article 112894

2021

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MYC rearrangement involving a novel non-immunoglobulin chromosomal locus in precursor B-cell acute lymphoblastic leukemia

Annals of Laboratory Medicine, 2012, 32(4), , pp.289-293

2012

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STS and PUDP Deletion Identified by Targeted Panel Sequencing with CNV Analysis in X-Linked Ichthyosis: A Case Report and Literature Review

Genes, 2023-10, Vol.14 (10), p.1925

2023

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The Mechanism of Allelic Competition in the ABO 547G>A Mutant is Associated with Decreased Activity of Glycosyltransferase B

Annals of clinical and laboratory science, 2016, Vol.46 (1), p.106-109

2016

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N-acetylcysteine reduce the stress induced by cold storage of platelets: A potential way to extend shelf life of platelets

Transfusion and apheresis science, 2021-04, Vol.60 (2), p.103039-103039, Article 103039

2021

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A double mutation of the ryanodine receptor type 1 gene in a malignant hyperthermia family with multiminicore myopathy

Journal of Clinical Neurology, 2008, 4(3), , pp.123-130

2008

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A loss function approach to group preference aggregation in the AHP

A novel variant of the POLR3A gene in a patient with hypomyelinating POLR3-related leukodystrophy

Diversity of Clinical and Molecular Characteristics in Korean Patients with 16p11.2 Microdeletion Syndrome

Isolation of EpCAM+/CD133− hepatic progenitor cells

Identification of a novel U2HR mutation in a Korean woman with Marie Unna hereditary hypotrichosis

Clinical and Genetic Characteristics of Early and Advanced Gastric Cancer

Isolation and Genetic Characterization of Orientia tsutsugamushi from Scrub Typhus Patients in Gyeongsangnam-do, Korea

Accuracy Validation of the Elecsys HBsAg II Quant Assay and Its Utility in Resolving Equivocal Qualitative HBsAg Results

Copy number variation analysis using next-generation sequencing identifies the CFHR3/CFHR1 deletion in atypical hemolytic uremic syndrome: a case report

A NOVEL C.800G>C VARIANT OF THE ITM2B GENE IN FAMILIAL KOREAN DEMENTIA

Clinical Features and Risk Factors Associated With 30-Day Mortality in Patients With Pneumonia Caused by Hypervirulent Klebsiella pneumoniae (hvKP)

The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructure

Case Report: Novel Likely Pathogenic ACTN2 Variant Causing Heterogeneous Phenotype in a Korean Family With Left Ventricular Non-compaction

Case report: Compound heterozygosity in PKLR gene with a large exon deletion and a novel rare p.Gly536Asp variant as a cause of severe pyruvate kinase deficiency

Dermabacter jinjuensis sp. nov., a novel species of the genus Dermabacter isolated from a clinical specimen

Seroprevalence of Neutralizing Antibodies against Japanese Encephalitis Virus among Adolescents and Adults in Korea: A Prospective Multicenter Study

SPA0355 prevents ovariectomy-induced bone loss in mice

A case of torsion of a mucinous cystadenoma in triple-X syndrome with pure gonadal dysgenesis

Insights into Platelet Storage and the Need for Multiple Approaches

Paper-based multiplex analytical device for simultaneous detection of Clostridioides difficile toxins and glutamate dehydrogenase

MYC rearrangement involving a novel non-immunoglobulin chromosomal locus in precursor B-cell acute lymphoblastic leukemia

STS and PUDP Deletion Identified by Targeted Panel Sequencing with CNV Analysis in X-Linked Ichthyosis: A Case Report and Literature Review

The Mechanism of Allelic Competition in the ABO 547G>A Mutant is Associated with Decreased Activity of Glycosyltransferase B

N-acetylcysteine reduce the stress induced by cold storage of platelets: A potential way to extend shelf life of platelets

A double mutation of the ryanodine receptor type 1 gene in a malignant hyperthermia family with multiminicore myopathy

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