송재우
#진단혈액학#혈전지혈#혈액종양학
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학력
ㆍ 연세대학교 의과대학 의학사(1997)
ㆍ 연세대학교 의과대학 석사 (2000)
ㆍ 연세대학교 의과대학 박사 (2011)
ㆍ 연세대학교 의과대학 석사 (2000)
ㆍ 연세대학교 의과대학 박사 (2011)
경력
ㆍ 2002-2004 연세의대 가정의학교실 강사
ㆍ 2004-2006 용인세브란스병원 진단검사의학과 과장
ㆍ 2006-2009 연세의대 진단검사의학교실 전임강사
ㆍ 2009-2014 연세의대 진단검사의학교실 조교수
ㆍ 2014-2020 연세의대 진단검사의학교실 부교수
ㆍ 2020-현재 연세의대 진단검사의학교실 교수
ㆍ 2006-현재 세브란스병원 진단검사의학과 교수
ㆍ 2004-2006 용인세브란스병원 진단검사의학과 과장
ㆍ 2006-2009 연세의대 진단검사의학교실 전임강사
ㆍ 2009-2014 연세의대 진단검사의학교실 조교수
ㆍ 2014-2020 연세의대 진단검사의학교실 부교수
ㆍ 2020-현재 연세의대 진단검사의학교실 교수
ㆍ 2006-현재 세브란스병원 진단검사의학과 교수
논문
Measurement of thrombus precursor protein in septic patients with disseminated intravascular coagulation and liver disease
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL 87/10 :1062-1067,2002
Plasma factor XIII activity in patients with disseminated intravascular coagulation
YONSEI MEDICAL JOURNAL 47/2 :196-200,2006
Plasma level of IL-6 and its relationship to procoagulant and fibrinolytic markers in acute ischemic stroke
YONSEI MEDICAL JOURNAL 47/2 :201-206,2006
늑막삼출과 주변 림프절 침범이 동반된 다발성골수종 1예
대한혈액학회지 41/1 :6-6,2006
t(5;12)(q13;p13) in acute myeloid leukemia with preceding granulocytic sarcoma
CANCER GENETICS AND CYTOGENETICS 177/2 :158-160,2007
자동혈구분석기 Cell-Dyn Sapphire의 평가
대한진단검사의학회지(The Korean Journal of Laboratory Medicine) 27/3 :162-168,2007
한국 von Willebrand병 환자의 von Willebrand 인자 유전자 돌연변이 조사
대한진단검사의학회지(The Korean Journal of Laboratory Medicine) 27/3 :169-176,2007
Anti-PF4/Heparin 항체 양성의 헤파린 유도 혈소판감소증 1예
대한혈액학회지 42/1 :10-10,2007
A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia
CANCER GENETICS AND CYTOGENETICS 179/2 :132-135,2007
Diagnosis of overt disseminated intravascular coagulation: A comparative study using criteria from the international society versus the Korean Society on Thrombosis and Hemostasis
YONSEI MEDICAL JOURNAL 48/4 :595-600,2007
Preceding orbital granulocytic sarcoma in an adult patient with acute myelogenous leukemia with t(8;21): a case study and review of the literature
Cancer Genetics And Cytogenetics 185/ :51-54,2008
Complex t(8;1.9;21)(q22;p13;q22) as a sole abnormality in a patient with de novo acute myeloid leukemia
Cancer Genetics And Cytogenetics 185/ :109-112,2008
Acute erythroleukemia with der(1;7)(q10;p10) as a sole acquired abnormality after treatment with azathioprine
Cancer Genetics And Cytogenetics 186/ :58-60,2008
Linear Relationship between ADAMTS13 Activity and Platelet Dynamics Even Before Severe Thrombocytopenia
Annals Of Clinical And Laboratory Science 38/ :368-375,2008
Transfusion-associated iron overload as a predictive factor for poor stem cell mobilization in patients with haematological malignancies
Transfusion Medicine 18/ :97-103,2008
Analysis of clinical presentations of Bruton Disease: A review of 20 years of accumulated data from pediatric patients at Severance Hospital
Yonsei Medical Journal 49/1 :28-36,2008
Rare translocations involving chromosome band 8p11 in myeloid neoplasms
Cancer Genetics And Cytogenetics 186/ :127-129,2008
Trisomy 8 in an elderly patient with acute lymphoblastic leukemia as a sole abnormality
Cancer Genetics And Cytogenetics 187/ :57-58,2008
듀센형근이영양증 유전자의 결실 돌연변이 검출을 위한 Dual Priming Oligonucleotide 다중 PCR법의 평가
Korean Journal Of Laboratory Medicine 28/5 :386-391,2008
Acute promyelocytic leukemia relapsing as secondary acute myelogenous leukemia with translocation t(3;21)(q26;q22) and RUNX1-MDS1-EVI1 fusion transcript
Cancer Genetics And Cytogenetics 187/2 :61-73,2008
A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer
Cancer Genetics And Cytogenetics 182/2 :136-139,2008
8번 염색체 사체성을 보인 급성단구성백혈병 1예
Korean Journal Of Laboratory Medicine 28/4 :262-266,2008
Paracentric inversion-associated t(8;21) variant in de novo acute myelogenous leukemia: characteristic patterns of conventional cytogenetics, FISH, and multicolor banding analysis
Cancer Genetics And Cytogenetics 183/1 :72-76,2008
8p11 myeloproliferative syndrome preceded by t(8;9)(p11;q33), CEP110/FGFR1 fusion transcript: morphologic, molecular, and cytogenetic characterization of myeloid neoplasms associated with eosinophilia and FGFR1 abnormality
Cancer Genetics And Cytogenetics 181/ :93-99,2008
MLL rearrangement with t(6;11)(q15;q23) as a sole abnormality in a patient with de novo acute myeloid leukemia: conventional cytogenetics, FISH, and multicolor FISH analyses for detection of rare MLL-related chromosome abnormalities
Cancer Genetics And Cytogenetics 187/ :50-53,2008
Transfusion-Associated Iron Overload as an Adverse Risk Factor for Transplantation Outcome in Patients Undergoing Reduced-Intensity Stem Cell Transplantation for Myeloid Malignancies
Acta Haematologica 120/3 :182-189,2008
Three new nonsense mutations of MLH1 and MSH2 genes in Korean families with hereditary nonpolyposis colorectal cancer
Cancer Genetics and Cytogenetics 188/ :61-64,2009
Acute promyelocytic leukemia with insertion of PML exon 7a and partial deletion of exon 3 of RARA: a novel variant transcript related to aggressive course and not detected with real-time polymerase chain reaction analysis
Cancer Genetics and Cytogenetics 188/ :103-107,2009
Biphenotypic acute leukemia with b2a2 fusion transcript and trisomy 21
Cancer Genetics and Cytogenetics 188/ :129-131,2009
Acute promyelocytic leukemia in early pregnancy with translocation t(15;17) and variant PML/RARA fusion transcripts
Cancer Genetics and Cytogenetics 188/ :48-51,2009
JAK2 V617F/C618R mutation in a patient with polycythemia vera: A case study and review of the literature
Cancer Genetics and Cytogenetics 189/ :43-47,2009
Hereditary protein S deficiency from a novel large deletion mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification (MLPA)
Thrombosis Research 123/5 :793-795,2009
A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family
Blood Coagulation & Fibrinolysis 20/ :150-156,2009
Therapy-Related Myelodysplastic Syndrome/Acute Myeloid Leukemia after Treatment with Temozolomide in a Patient with Glioblastoma Multiforme
Annals Of Clinical And Laboratory Science 39/4 :392-398,2009
Therapy-related acute lymphoblastic leukemia with t(9;22)(q34;q11.2): a case study and review of the literature
Cancer Genetics and Cytogenetics 191/ :51-54,2009
Concomitant Isochromosome 17q and Trisomy 14 in a Patient with Myelodysplastic Syndrome in Leukemic Transformation
Annals Of Clinical And Laboratory Science 39/2 :176-181,2009
A Novel PHEX Mutation in a Korean Patient with Sporadic Hypophosphatemic Rickets
Annals Of Clinical And Laboratory Science 39/2 :182-187,2009
Two case reports of 1q triplication in myeloproliferative neoplasms
Cancer Genetics and Cytogenetics 191/2 :111-112,2009
Non-age related Y chromosome loss in an elderly patient with acute promyelocytic leukemia
Leukemia Research 33/ :e114-e115,2009
der(1)t(1;19)(p13;p13.1) in two elderly patients with myeloid neoplasms: New case reports and review of the literature
Leukemia Research 33/8 :128-131,2009
Concomitant t(3;3)(q21;q26), trisomy 19, and E255V mutation associated with imatinib mesylate resistance in chronic myelogenous leukemia
Cancer Genetics and Cytogenetics 190/ :46-48,2009
Detection of a novel CBFB/MYH11 variant fusion transcript (K-type) showing partial insertion of exon 6 of CBFB gene using two commercially available multiplex RT-PCR kits
Cancer Genetics and Cytogenetics 189/2 :87-92,2009
A tandem triplication, trp(1)(q21q32), in a patient with follicular lymphoma: a case study and review of the literature
Cancer Genetics and Cytogenetics 189/ :127-131,2009
BCR/ABL rearrangement with b3a3 fusion transcript in a case of childhood acute lymphoblastic leukemia
Cancer Genetics and Cytogenetics 189/ :132-137,2009
Chronic Myelomonocytic Leukemia with der(9)t(1;9)(q11;q34) as a Sole Abnormality
Annals Of Clinical And Laboratory Science 39/3 :307-312,2009
Detection of FUS-ERG chimeric transcript in two cases of acute myeloid leukemia with t(16;21)(p11.2;q22) with unusual characteristics
Cancer Genetics and Cytogenetics 194/2 :111-118,2009
CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia
Cancer Genetics and Cytogenetics 195/1 :94-95,2009
Therapy-related myelodysplastic syndrome with der(17)t(12;17)(q13;p13) as a new recurrent cytogenetic abnormality after treatment for chronic lymphocytic leukemia
Leukemia Research 33/7 :1001-1004,2009
Association between acute promyelocytic leukemia and ring chromosome 6
Cancer Genetics and Cytogenetics 192/1 :48-50,2009
Three-way translocation involving MLL, MLLT1, and a novel third partner, NRXN1, in a patient with acute lymphoblastic leukemia and t(2;19;11) (p12;p13.3;q23)
Cancer Genetics and Cytogenetics 197/1 :32-38,2010
A novel t(1;12)(q21;q24) in a patient with myelodysplastic syndrome
Annals of Hematology 89/ :513-516,2010
Short Report: Automated Detection of Malaria-Associated Pseudoeosinophilia and Abnormal WBC Scattergram by the Sysmex XE-2100 Hematology Analyzer: A Clinical Study with 1,801 Patients and Real-Time Quantitative PCR Analysis in Vivax Malaria-Endemic
American Journal of Tropical Medicine and Hygiene 82/3 :412-414,2010
Agranular platelets as a cardinal feature of ARC syndrome
Journal Of Pediatric Hematology Oncology 32/4 :253-258,2010
An SRY-Deleted XXY Female Resulting from a Paternally Inherited t(Y;22)
Annals of Clinical and Laboratory Science 40/3 :295-299,2010
Molecular characterization of alternative SET-NUP214 fusion transcripts in a case of acute undifferentiated leukemia
Cancer Genetics and Cytogenetics 201/2 :73-80,2010
Prognostic significance of trisomy 6 in an adult acute myeloid leukemia with t(8;21)
Cancer Genetics and Cytogenetics 202/2 :141-143,2010
Constitutional pericentric inversion 9 and hematological disorders: a Korean tertiary institution's experience over eight years
Annals of Clinical and Laboratory Science 40/3 :273-277,2010
Constitutional Pericentric Inversion 9 in Korean Patients with Chronic Myelogenous Leukemia
KOREAN JOURNAL OF LABORATORY MEDICINE 30/3 :218-223,2010
Comparison of Effects of Two Different Formulations of Clopidogrel Bisulfate Tablets on Platelet Aggregation and Bleeding Time in Healthy Korean Volunteers: A Single-Dose, Randomized, Open-Label, 1-Week, Two-Period, Phase IV Crossover Study
Clinical Therapeutics 32/9 :1664-1673,2010
Molecular cytogenetic analysis of Korean patients with Waldenstrom macroglobulinemia
Cancer Genetics and Cytogenetics 197/2 :117-121,2010
Diagnosis of non-overt disseminated intravascular coagulation made according to the International Society on Thrombosis and Hemostasis criteria with some modifications
대한혈액학회지 45/4 :260-263,2010
Case Report: A Heparin Binding Site Arg79Cys Missense Mutation in the SERPINC1 Gene in a Korean Patient with Hereditary Antithrombin Deficiency
ANNALS OF CLINICAL AND LABORATORY SCIENCE 41/1 :89-92,2011
Rapid Identification of Thrombocytopenia-Associated Multiple Organ Failure Using Red Blood Cell Parameters and a Volume/Hemoglobin Concentration Cytogram
YONSEI MEDICAL JOURNAL 52/5 :845-850,2011
Acute Promyelocytic Leukemia with Trisomy 8 and del(9)(q22) after Treatment of Cervical Cancer with Concurrent Chemoradiotherapy: A Case Report
ONKOLOGIE 34/7 :388-390,2011
DELTA NEUTROPHIL INDEX: A PROMISING DIAGNOSTIC AND PROGNOSTIC MARKER FOR SEPSIS
SHOCK 37/ :242-246,2012
Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect
CLINICAL GENETICS 82/2 :180-186,2012
CD5-negative Blastoid Variant Mantle Cell Lymphoma with Complex CCND1/IGH and MYC Aberrations
ANNALS OF LABORATORY MEDICINE 32/1 :95-98,2012
Fibrinogen residue gamma Ala341 is necessary for calcium binding and 'A-a' interactions
THROMBOSIS AND HAEMOSTASIS 107/5 :875-883,2012
Comparison Study of the Rates of Manual Peripheral Blood Smear Review From 3 Automated Hematology Analyzers, Unicel DxH 800, ADVIA 2120i, and XE 2100, Using International Consensus Group Guidelines
ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE 136/11 :1408-1413,2012
A Gly1609Arg Missense Mutation in the vWF Gene in a Korean Patient with von Willebrand Disease Type 2A
ANNALS OF CLINICAL AND LABORATORY SCIENCE 42/1 :98-102,2012
Image analysis of peripheral compression artefacts of ThinPrep? liquid-based cytology preparations
CYTOPATHOLOGY 24/2 :99-104,2013
Immature platelet fraction in diabetes mellitus and metabolic syndrome
THROMBOSIS RESEARCH 132/6 :692-695,2013
The instability of commercial control materials in quality control of mean corpuscular volume
CLINICA CHIMICA ACTA 434/- :11-15,2014
Analytical and clinical performance of a new point of care LABGEOIB D-dimer test for diagnosis of venous thromboembolism
ANNALS OF CLINICAL AND LABORATORY SCIENCE 44/3 :254-261,2014
Monoclonal and polyclonal gammopathy measured by serum free light chain and immunofixation subdivide the clinical outcomes of diffuse large B-cell lymphoma according to molecular classification
ANNALS OF HEMATOLOGY 93/11 :1867-1877,2014
Comparison of Prothrombin Time Derived From CoaguChek XS and Laboratory Test According to Fibrinogen Level
JOURNAL OF CLINICAL LABORATORY ANALYSIS 29/1 :28-31,2015
Quantitative Influence of ABO Blood Groups on Factor VIII and Its Ratio to von Willebrand Factor, Novel Observations from an ARIC Study of 11,673 Subjects
PLOS ONE 10/8 :e0132626-,2015
Capillary-scale direct measurement of hemoglobin concentration of erythrocytes using photothermal angular light scattering
BIOSENSORS & BIOELECTRONICS 74/ :469-475,2015
Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposure
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY 467/11 :2243-2256,2015
Pretreatment Lymphopenia, Poor Performance Status, and Early Courses of Therapy Are Risk Factors for Severe Bacterial Infection in Patients with Multiple Myeloma during Treatment with Bortezomib-based Regimens
JOURNAL OF KOREAN MEDICAL SCIENCE 31/4 :510-518,2016
The prognostic significance of monoclonal immunoglobulin gene rearrangement in conjunction with histologic B-cell aggregates in the bone marrow of patients with diffuse large B-cell lymphoma
CANCER MEDICINE 5/6 :1066-1073,2016
Magnetic bead-based nucleic acid purification kit: Clinical application and performance evaluation in stool specimens
JOURNAL OF MICROBIOLOGICAL METHODS 124/ :62-68,2016
Association of Single Nucleotide Polymorphisms in the ST3GAL4 Gene with VWF Antigen and Factor VIII Activity
PLOS ONE 11/9 :e0160757-,2016
Clinical Utility of Bone Marrow Study in Gaucher Disease: A Case Report of Gaucher Disease Type 3 With Intractable Myoclonic Seizures
ANNALS OF LABORATORY MEDICINE 36/2 :177-179,2016
Automated CH50 liposome-based immunoassay: consideration in dilution and validation of reference interval
CLINICAL CHEMISTRY AND LABORATORY MEDICINE 54/10 :e309-e312,2016
Neutrophil to lymphocyte ratio and platelet to lymphocyte ratio as diagnostic markers for pneumonia severity
BRITISH JOURNAL OF BIOMEDICAL SCIENCE 73/3 :140-142,2016
A Rapid and Chemical-free Hemoglobin Assay with Photothermal Angular Light Scattering
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS 118/e5500 :1-6,2016
Smart Forensic Phone: Colorimetric analysis of a bloodstain for age estimation using a smartphone
SENSORS AND ACTUATORS B-CHEMICAL 243/ :221-225,2017
Color-coded LED microscopy for quantitative phase imaging: Implementation and application to sperm motility analysis
METHODS 136/ :66-74,2018
Platelet storage induces accelerated desialylation of platelets and increases hepatic thrombopoietin production
JOURNAL OF TRANSLATIONAL MEDICINE 16/1 :199-208,2018
HBsAg-Negative, Anti-HBc?Negative Patients Still Have a Risk of Hepatitis B Virus?Related Hepatitis after Autologous Stem Cell Transplantation for Multiple Myeloma or Malignant Lymphoma
CANCER RESEARCH AND TREATMENT 50/4 :1,121-1,129,2018
Biometric Image Analysis for Quantitation of Dividing Platelets
MICROMACHINES 10/1 :1-13,2018
Highly sensitive and accurate estimation of bloodstain age using smartphone
BIOSENSORS & BIOELECTRONICS 130/ :414-419,2019
Anti?phospholipid antibody syndrome occurrence in patients with persistent anti?phospholipid antibodies
RHEUMATOLOGY INTERNATIONAL 39/8 :1,359-1,367,2019
Early Cytomegalovirus Reactivation and Expansion of CD56brightCD16dim/?DNAM1+ Natural Killer Cells Are Associated with Antileukemia Effect after Haploidentical Stem Cell Transplantation in Acute Leukemia
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION 25/10 :2,070-2,078,2019
Automatically Controlled Microfluidic System for Continuous Separation of Rare Bacteria from Blood
CYTOMETRY PART A 95/11 :1,135-1,144,2019
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL 87/10 :1062-1067,2002
Plasma factor XIII activity in patients with disseminated intravascular coagulation
YONSEI MEDICAL JOURNAL 47/2 :196-200,2006
Plasma level of IL-6 and its relationship to procoagulant and fibrinolytic markers in acute ischemic stroke
YONSEI MEDICAL JOURNAL 47/2 :201-206,2006
늑막삼출과 주변 림프절 침범이 동반된 다발성골수종 1예
대한혈액학회지 41/1 :6-6,2006
t(5;12)(q13;p13) in acute myeloid leukemia with preceding granulocytic sarcoma
CANCER GENETICS AND CYTOGENETICS 177/2 :158-160,2007
자동혈구분석기 Cell-Dyn Sapphire의 평가
대한진단검사의학회지(The Korean Journal of Laboratory Medicine) 27/3 :162-168,2007
한국 von Willebrand병 환자의 von Willebrand 인자 유전자 돌연변이 조사
대한진단검사의학회지(The Korean Journal of Laboratory Medicine) 27/3 :169-176,2007
Anti-PF4/Heparin 항체 양성의 헤파린 유도 혈소판감소증 1예
대한혈액학회지 42/1 :10-10,2007
A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia
CANCER GENETICS AND CYTOGENETICS 179/2 :132-135,2007
Diagnosis of overt disseminated intravascular coagulation: A comparative study using criteria from the international society versus the Korean Society on Thrombosis and Hemostasis
YONSEI MEDICAL JOURNAL 48/4 :595-600,2007
Preceding orbital granulocytic sarcoma in an adult patient with acute myelogenous leukemia with t(8;21): a case study and review of the literature
Cancer Genetics And Cytogenetics 185/ :51-54,2008
Complex t(8;1.9;21)(q22;p13;q22) as a sole abnormality in a patient with de novo acute myeloid leukemia
Cancer Genetics And Cytogenetics 185/ :109-112,2008
Acute erythroleukemia with der(1;7)(q10;p10) as a sole acquired abnormality after treatment with azathioprine
Cancer Genetics And Cytogenetics 186/ :58-60,2008
Linear Relationship between ADAMTS13 Activity and Platelet Dynamics Even Before Severe Thrombocytopenia
Annals Of Clinical And Laboratory Science 38/ :368-375,2008
Transfusion-associated iron overload as a predictive factor for poor stem cell mobilization in patients with haematological malignancies
Transfusion Medicine 18/ :97-103,2008
Analysis of clinical presentations of Bruton Disease: A review of 20 years of accumulated data from pediatric patients at Severance Hospital
Yonsei Medical Journal 49/1 :28-36,2008
Rare translocations involving chromosome band 8p11 in myeloid neoplasms
Cancer Genetics And Cytogenetics 186/ :127-129,2008
Trisomy 8 in an elderly patient with acute lymphoblastic leukemia as a sole abnormality
Cancer Genetics And Cytogenetics 187/ :57-58,2008
듀센형근이영양증 유전자의 결실 돌연변이 검출을 위한 Dual Priming Oligonucleotide 다중 PCR법의 평가
Korean Journal Of Laboratory Medicine 28/5 :386-391,2008
Acute promyelocytic leukemia relapsing as secondary acute myelogenous leukemia with translocation t(3;21)(q26;q22) and RUNX1-MDS1-EVI1 fusion transcript
Cancer Genetics And Cytogenetics 187/2 :61-73,2008
A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer
Cancer Genetics And Cytogenetics 182/2 :136-139,2008
8번 염색체 사체성을 보인 급성단구성백혈병 1예
Korean Journal Of Laboratory Medicine 28/4 :262-266,2008
Paracentric inversion-associated t(8;21) variant in de novo acute myelogenous leukemia: characteristic patterns of conventional cytogenetics, FISH, and multicolor banding analysis
Cancer Genetics And Cytogenetics 183/1 :72-76,2008
8p11 myeloproliferative syndrome preceded by t(8;9)(p11;q33), CEP110/FGFR1 fusion transcript: morphologic, molecular, and cytogenetic characterization of myeloid neoplasms associated with eosinophilia and FGFR1 abnormality
Cancer Genetics And Cytogenetics 181/ :93-99,2008
MLL rearrangement with t(6;11)(q15;q23) as a sole abnormality in a patient with de novo acute myeloid leukemia: conventional cytogenetics, FISH, and multicolor FISH analyses for detection of rare MLL-related chromosome abnormalities
Cancer Genetics And Cytogenetics 187/ :50-53,2008
Transfusion-Associated Iron Overload as an Adverse Risk Factor for Transplantation Outcome in Patients Undergoing Reduced-Intensity Stem Cell Transplantation for Myeloid Malignancies
Acta Haematologica 120/3 :182-189,2008
Three new nonsense mutations of MLH1 and MSH2 genes in Korean families with hereditary nonpolyposis colorectal cancer
Cancer Genetics and Cytogenetics 188/ :61-64,2009
Acute promyelocytic leukemia with insertion of PML exon 7a and partial deletion of exon 3 of RARA: a novel variant transcript related to aggressive course and not detected with real-time polymerase chain reaction analysis
Cancer Genetics and Cytogenetics 188/ :103-107,2009
Biphenotypic acute leukemia with b2a2 fusion transcript and trisomy 21
Cancer Genetics and Cytogenetics 188/ :129-131,2009
Acute promyelocytic leukemia in early pregnancy with translocation t(15;17) and variant PML/RARA fusion transcripts
Cancer Genetics and Cytogenetics 188/ :48-51,2009
JAK2 V617F/C618R mutation in a patient with polycythemia vera: A case study and review of the literature
Cancer Genetics and Cytogenetics 189/ :43-47,2009
Hereditary protein S deficiency from a novel large deletion mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification (MLPA)
Thrombosis Research 123/5 :793-795,2009
A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family
Blood Coagulation & Fibrinolysis 20/ :150-156,2009
Therapy-Related Myelodysplastic Syndrome/Acute Myeloid Leukemia after Treatment with Temozolomide in a Patient with Glioblastoma Multiforme
Annals Of Clinical And Laboratory Science 39/4 :392-398,2009
Therapy-related acute lymphoblastic leukemia with t(9;22)(q34;q11.2): a case study and review of the literature
Cancer Genetics and Cytogenetics 191/ :51-54,2009
Concomitant Isochromosome 17q and Trisomy 14 in a Patient with Myelodysplastic Syndrome in Leukemic Transformation
Annals Of Clinical And Laboratory Science 39/2 :176-181,2009
A Novel PHEX Mutation in a Korean Patient with Sporadic Hypophosphatemic Rickets
Annals Of Clinical And Laboratory Science 39/2 :182-187,2009
Two case reports of 1q triplication in myeloproliferative neoplasms
Cancer Genetics and Cytogenetics 191/2 :111-112,2009
Non-age related Y chromosome loss in an elderly patient with acute promyelocytic leukemia
Leukemia Research 33/ :e114-e115,2009
der(1)t(1;19)(p13;p13.1) in two elderly patients with myeloid neoplasms: New case reports and review of the literature
Leukemia Research 33/8 :128-131,2009
Concomitant t(3;3)(q21;q26), trisomy 19, and E255V mutation associated with imatinib mesylate resistance in chronic myelogenous leukemia
Cancer Genetics and Cytogenetics 190/ :46-48,2009
Detection of a novel CBFB/MYH11 variant fusion transcript (K-type) showing partial insertion of exon 6 of CBFB gene using two commercially available multiplex RT-PCR kits
Cancer Genetics and Cytogenetics 189/2 :87-92,2009
A tandem triplication, trp(1)(q21q32), in a patient with follicular lymphoma: a case study and review of the literature
Cancer Genetics and Cytogenetics 189/ :127-131,2009
BCR/ABL rearrangement with b3a3 fusion transcript in a case of childhood acute lymphoblastic leukemia
Cancer Genetics and Cytogenetics 189/ :132-137,2009
Chronic Myelomonocytic Leukemia with der(9)t(1;9)(q11;q34) as a Sole Abnormality
Annals Of Clinical And Laboratory Science 39/3 :307-312,2009
Detection of FUS-ERG chimeric transcript in two cases of acute myeloid leukemia with t(16;21)(p11.2;q22) with unusual characteristics
Cancer Genetics and Cytogenetics 194/2 :111-118,2009
CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia
Cancer Genetics and Cytogenetics 195/1 :94-95,2009
Therapy-related myelodysplastic syndrome with der(17)t(12;17)(q13;p13) as a new recurrent cytogenetic abnormality after treatment for chronic lymphocytic leukemia
Leukemia Research 33/7 :1001-1004,2009
Association between acute promyelocytic leukemia and ring chromosome 6
Cancer Genetics and Cytogenetics 192/1 :48-50,2009
Three-way translocation involving MLL, MLLT1, and a novel third partner, NRXN1, in a patient with acute lymphoblastic leukemia and t(2;19;11) (p12;p13.3;q23)
Cancer Genetics and Cytogenetics 197/1 :32-38,2010
A novel t(1;12)(q21;q24) in a patient with myelodysplastic syndrome
Annals of Hematology 89/ :513-516,2010
Short Report: Automated Detection of Malaria-Associated Pseudoeosinophilia and Abnormal WBC Scattergram by the Sysmex XE-2100 Hematology Analyzer: A Clinical Study with 1,801 Patients and Real-Time Quantitative PCR Analysis in Vivax Malaria-Endemic
American Journal of Tropical Medicine and Hygiene 82/3 :412-414,2010
Agranular platelets as a cardinal feature of ARC syndrome
Journal Of Pediatric Hematology Oncology 32/4 :253-258,2010
An SRY-Deleted XXY Female Resulting from a Paternally Inherited t(Y;22)
Annals of Clinical and Laboratory Science 40/3 :295-299,2010
Molecular characterization of alternative SET-NUP214 fusion transcripts in a case of acute undifferentiated leukemia
Cancer Genetics and Cytogenetics 201/2 :73-80,2010
Prognostic significance of trisomy 6 in an adult acute myeloid leukemia with t(8;21)
Cancer Genetics and Cytogenetics 202/2 :141-143,2010
Constitutional pericentric inversion 9 and hematological disorders: a Korean tertiary institution's experience over eight years
Annals of Clinical and Laboratory Science 40/3 :273-277,2010
Constitutional Pericentric Inversion 9 in Korean Patients with Chronic Myelogenous Leukemia
KOREAN JOURNAL OF LABORATORY MEDICINE 30/3 :218-223,2010
Comparison of Effects of Two Different Formulations of Clopidogrel Bisulfate Tablets on Platelet Aggregation and Bleeding Time in Healthy Korean Volunteers: A Single-Dose, Randomized, Open-Label, 1-Week, Two-Period, Phase IV Crossover Study
Clinical Therapeutics 32/9 :1664-1673,2010
Molecular cytogenetic analysis of Korean patients with Waldenstrom macroglobulinemia
Cancer Genetics and Cytogenetics 197/2 :117-121,2010
Diagnosis of non-overt disseminated intravascular coagulation made according to the International Society on Thrombosis and Hemostasis criteria with some modifications
대한혈액학회지 45/4 :260-263,2010
Case Report: A Heparin Binding Site Arg79Cys Missense Mutation in the SERPINC1 Gene in a Korean Patient with Hereditary Antithrombin Deficiency
ANNALS OF CLINICAL AND LABORATORY SCIENCE 41/1 :89-92,2011
Rapid Identification of Thrombocytopenia-Associated Multiple Organ Failure Using Red Blood Cell Parameters and a Volume/Hemoglobin Concentration Cytogram
YONSEI MEDICAL JOURNAL 52/5 :845-850,2011
Acute Promyelocytic Leukemia with Trisomy 8 and del(9)(q22) after Treatment of Cervical Cancer with Concurrent Chemoradiotherapy: A Case Report
ONKOLOGIE 34/7 :388-390,2011
DELTA NEUTROPHIL INDEX: A PROMISING DIAGNOSTIC AND PROGNOSTIC MARKER FOR SEPSIS
SHOCK 37/ :242-246,2012
Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect
CLINICAL GENETICS 82/2 :180-186,2012
CD5-negative Blastoid Variant Mantle Cell Lymphoma with Complex CCND1/IGH and MYC Aberrations
ANNALS OF LABORATORY MEDICINE 32/1 :95-98,2012
Fibrinogen residue gamma Ala341 is necessary for calcium binding and 'A-a' interactions
THROMBOSIS AND HAEMOSTASIS 107/5 :875-883,2012
Comparison Study of the Rates of Manual Peripheral Blood Smear Review From 3 Automated Hematology Analyzers, Unicel DxH 800, ADVIA 2120i, and XE 2100, Using International Consensus Group Guidelines
ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE 136/11 :1408-1413,2012
A Gly1609Arg Missense Mutation in the vWF Gene in a Korean Patient with von Willebrand Disease Type 2A
ANNALS OF CLINICAL AND LABORATORY SCIENCE 42/1 :98-102,2012
Image analysis of peripheral compression artefacts of ThinPrep? liquid-based cytology preparations
CYTOPATHOLOGY 24/2 :99-104,2013
Immature platelet fraction in diabetes mellitus and metabolic syndrome
THROMBOSIS RESEARCH 132/6 :692-695,2013
The instability of commercial control materials in quality control of mean corpuscular volume
CLINICA CHIMICA ACTA 434/- :11-15,2014
Analytical and clinical performance of a new point of care LABGEOIB D-dimer test for diagnosis of venous thromboembolism
ANNALS OF CLINICAL AND LABORATORY SCIENCE 44/3 :254-261,2014
Monoclonal and polyclonal gammopathy measured by serum free light chain and immunofixation subdivide the clinical outcomes of diffuse large B-cell lymphoma according to molecular classification
ANNALS OF HEMATOLOGY 93/11 :1867-1877,2014
Comparison of Prothrombin Time Derived From CoaguChek XS and Laboratory Test According to Fibrinogen Level
JOURNAL OF CLINICAL LABORATORY ANALYSIS 29/1 :28-31,2015
Quantitative Influence of ABO Blood Groups on Factor VIII and Its Ratio to von Willebrand Factor, Novel Observations from an ARIC Study of 11,673 Subjects
PLOS ONE 10/8 :e0132626-,2015
Capillary-scale direct measurement of hemoglobin concentration of erythrocytes using photothermal angular light scattering
BIOSENSORS & BIOELECTRONICS 74/ :469-475,2015
Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposure
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY 467/11 :2243-2256,2015
Pretreatment Lymphopenia, Poor Performance Status, and Early Courses of Therapy Are Risk Factors for Severe Bacterial Infection in Patients with Multiple Myeloma during Treatment with Bortezomib-based Regimens
JOURNAL OF KOREAN MEDICAL SCIENCE 31/4 :510-518,2016
The prognostic significance of monoclonal immunoglobulin gene rearrangement in conjunction with histologic B-cell aggregates in the bone marrow of patients with diffuse large B-cell lymphoma
CANCER MEDICINE 5/6 :1066-1073,2016
Magnetic bead-based nucleic acid purification kit: Clinical application and performance evaluation in stool specimens
JOURNAL OF MICROBIOLOGICAL METHODS 124/ :62-68,2016
Association of Single Nucleotide Polymorphisms in the ST3GAL4 Gene with VWF Antigen and Factor VIII Activity
PLOS ONE 11/9 :e0160757-,2016
Clinical Utility of Bone Marrow Study in Gaucher Disease: A Case Report of Gaucher Disease Type 3 With Intractable Myoclonic Seizures
ANNALS OF LABORATORY MEDICINE 36/2 :177-179,2016
Automated CH50 liposome-based immunoassay: consideration in dilution and validation of reference interval
CLINICAL CHEMISTRY AND LABORATORY MEDICINE 54/10 :e309-e312,2016
Neutrophil to lymphocyte ratio and platelet to lymphocyte ratio as diagnostic markers for pneumonia severity
BRITISH JOURNAL OF BIOMEDICAL SCIENCE 73/3 :140-142,2016
A Rapid and Chemical-free Hemoglobin Assay with Photothermal Angular Light Scattering
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS 118/e5500 :1-6,2016
Smart Forensic Phone: Colorimetric analysis of a bloodstain for age estimation using a smartphone
SENSORS AND ACTUATORS B-CHEMICAL 243/ :221-225,2017
Color-coded LED microscopy for quantitative phase imaging: Implementation and application to sperm motility analysis
METHODS 136/ :66-74,2018
Platelet storage induces accelerated desialylation of platelets and increases hepatic thrombopoietin production
JOURNAL OF TRANSLATIONAL MEDICINE 16/1 :199-208,2018
HBsAg-Negative, Anti-HBc?Negative Patients Still Have a Risk of Hepatitis B Virus?Related Hepatitis after Autologous Stem Cell Transplantation for Multiple Myeloma or Malignant Lymphoma
CANCER RESEARCH AND TREATMENT 50/4 :1,121-1,129,2018
Biometric Image Analysis for Quantitation of Dividing Platelets
MICROMACHINES 10/1 :1-13,2018
Highly sensitive and accurate estimation of bloodstain age using smartphone
BIOSENSORS & BIOELECTRONICS 130/ :414-419,2019
Anti?phospholipid antibody syndrome occurrence in patients with persistent anti?phospholipid antibodies
RHEUMATOLOGY INTERNATIONAL 39/8 :1,359-1,367,2019
Early Cytomegalovirus Reactivation and Expansion of CD56brightCD16dim/?DNAM1+ Natural Killer Cells Are Associated with Antileukemia Effect after Haploidentical Stem Cell Transplantation in Acute Leukemia
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION 25/10 :2,070-2,078,2019
Automatically Controlled Microfluidic System for Continuous Separation of Rare Bacteria from Blood
CYTOMETRY PART A 95/11 :1,135-1,144,2019
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