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Environmental surface testing for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) during prolonged isolation of an asymptomatic carrier

Infection control and hospital epidemiology, 2020-11, Vol.41 (11), p.1328-1330

2020

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Human Granulocytic Anaplasmosis Diagnosed Based on a Peripheral Blood Smear Test in South Korea: a Case Report

Japanese Journal of Infectious Diseases, 2020/11/30, Vol.73(6), pp.469-472

2020

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What is new in acute myeloid leukemia classification?

Blood Research, 2024, 59(2), , pp.15-15

Park, Hee Sue

2024

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Short telomere length and its correlation with gene mutations in myelodysplastic syndrome

Journal of hematology and oncology, 2016-07, Vol.9 (1), p.62-62, Article 62

2016

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Serial Analysis and Comparison of Mutation Profiles in Decitabine-treated Myeloid Sarcoma and Subsequent Acute Myeloid Leukemia Using Next-Generation Sequencing

Annals of Laboratory Medicine, 2022, 42(5), , pp.602-605

2022

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TP53 mutation is a high-risk factor for RichterÊs syndrome based on circulating tumor DNA

Blood Research, 2023, 58(4), , pp.228-231

2023

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Efficacy of ferric carboxymaltose or darbepoetin alfa for chemotherapy-induced anemia in patients with esophagogastric or pancreaticobiliary cancer: a retrospective comparative study

Therapeutic advances in medical oncology, 2024-01, Vol.16, p.17588359241265209

2024

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Coagulopathy profiles and their correlation with molecular viral burden in patients with COVID-19

Blood Research, 2021, 56(1), , pp.56-58

2021

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A Case of Acquired Amegakaryocytic Thrombocytopenia with Anti-c-mpl Autoantibody: Comparison with Idiopathic Thrombocytopenic Purpura

Acta haematologica, 2019-11, Vol.142 (4), p.239-243

2019

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SARS-CoV-2 molecular diagnostic point-of-care testing based on loop-mediated isothermal amplification: A prospective, single-center validation study

Heliyon, 2023-03, Vol.9 (3), p.e14564-e14564, Article e14564

2023

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Korean clinical practice guidelines for the diagnosis of hereditary hemolytic anemia

Blood Research, 2022, 57(2), , pp.86-94

2022

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Clinical utility of chromosomal microarray analysis to detect copy number variants: Experience in a single tertiary hospital

Journal of genetic medicine, 2021-06, Vol.18 (1), p.31-37

2021

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Differences in seroprevalence between epicenter and non-epicenter areas of the COVID-19 outbreak in South Korea

The Journal of Microbiology, 2021, 59(5), , pp.530-533

2021

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Mutation of ten-eleven translocation-2 is associated with increased risk of autoimmune disease in patients with myelodysplastic syndrome

The Korean Journal of Internal Medicine, 2020, 35(2), , pp.457-464

2020

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The importance of critically short telomere in myelodysplastic syndrome

Biomarker research, 2022-11, Vol.10 (1), p.1-79, Article 79

2022

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Increased Apoptotic Activity in Low-Risk Myelodysplastic Syndrome

Journal of clinical medicine, 2022-08, Vol.11 (15), p.4604

2022

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Identification of candidate gene variants of monogenic diabetes using targeted panel sequencing in early onset diabetes patients

BMJ open diabetes research & care, 2021-06, Vol.9 (1), p.e002217

2021

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Nocardia abscessus Cutaneous Abscess: A Case Report and Review of the Literature

Annals of clinical microbiology, 2018-09, Vol.21 (3), p.64

2018

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P-119 The role of lenalidomide-dexamethasone therapy in elderly patients with multiple myeloma in clinical practice: comparison with bortezomib-based therapy

Clinical lymphoma, myeloma and leukemia, 2023-09, Vol.23, p.S101-S101

2023

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Prognostic Role of Cleaved Caspase-3 Reflecting Apoptosis in MDS Patients

Blood, 2022-11, Vol.140 (Supplement 1), p.12343-12344

2022

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Compound Heterozygous VPS13A Variants in a Patient with Neuroacanthocytosis: A Case Report and Review of the Literature

Laboratory medicine, 2022-07, Vol.53 (4), p.433

2022

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Compound Heterozygous VPS13A Variants in a Patient with Neuroacanthocytosis: A Case Report and Review of the Literature

Laboratory medicine, 2022-07, Vol.53 (4), p.433-435

2022

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Usefulness of Genetic Aberration and Shorter Telomere Length in Myelodysplastic Syndrome: A Pilot Study

Laboratory medicine, 2023-03, Vol.54 (2), p.199-205

2023

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The new diagnostic criteria for myelodysplasia-related acute myeloid leukemia is useful for predicting clinical outcome: comparison of the 4th and 5th World Health Organization classifications

Annals of hematology, 2022-12, Vol.101 (12), p.2645-2654

2022

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The Discordance between G-Banding Karyotyping and Microarray in Structural Abnormality

Clinical laboratory (Heidelberg), 2023-01, Vol.69 (12)

2023

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Environmental surface testing for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) during prolonged isolation of an asymptomatic carrier

Human Granulocytic Anaplasmosis Diagnosed Based on a Peripheral Blood Smear Test in South Korea: a Case Report

What is new in acute myeloid leukemia classification?

Short telomere length and its correlation with gene mutations in myelodysplastic syndrome

Serial Analysis and Comparison of Mutation Profiles in Decitabine-treated Myeloid Sarcoma and Subsequent Acute Myeloid Leukemia Using Next-Generation Sequencing

TP53 mutation is a high-risk factor for RichterÊs syndrome based on circulating tumor DNA

Efficacy of ferric carboxymaltose or darbepoetin alfa for chemotherapy-induced anemia in patients with esophagogastric or pancreaticobiliary cancer: a retrospective comparative study

Coagulopathy profiles and their correlation with molecular viral burden in patients with COVID-19

A Case of Acquired Amegakaryocytic Thrombocytopenia with Anti-c-mpl Autoantibody: Comparison with Idiopathic Thrombocytopenic Purpura

SARS-CoV-2 molecular diagnostic point-of-care testing based on loop-mediated isothermal amplification: A prospective, single-center validation study

Korean clinical practice guidelines for the diagnosis of hereditary hemolytic anemia

Clinical utility of chromosomal microarray analysis to detect copy number variants: Experience in a single tertiary hospital

Differences in seroprevalence between epicenter and non-epicenter areas of the COVID-19 outbreak in South Korea

Mutation of ten-eleven translocation-2 is associated with increased risk of autoimmune disease in patients with myelodysplastic syndrome

The importance of critically short telomere in myelodysplastic syndrome

Increased Apoptotic Activity in Low-Risk Myelodysplastic Syndrome

Identification of candidate gene variants of monogenic diabetes using targeted panel sequencing in early onset diabetes patients

Nocardia abscessus Cutaneous Abscess: A Case Report and Review of the Literature

P-119 The role of lenalidomide-dexamethasone therapy in elderly patients with multiple myeloma in clinical practice: comparison with bortezomib-based therapy

Prognostic Role of Cleaved Caspase-3 Reflecting Apoptosis in MDS Patients

Compound Heterozygous VPS13A Variants in a Patient with Neuroacanthocytosis: A Case Report and Review of the Literature

Compound Heterozygous VPS13A Variants in a Patient with Neuroacanthocytosis: A Case Report and Review of the Literature

Usefulness of Genetic Aberration and Shorter Telomere Length in Myelodysplastic Syndrome: A Pilot Study

The new diagnostic criteria for myelodysplasia-related acute myeloid leukemia is useful for predicting clinical outcome: comparison of the 4th and 5th World Health Organization classifications

The Discordance between G-Banding Karyotyping and Microarray in Structural Abnormality

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