ANTIOXIDANTS-BASEL 2021 10.3390/antiox10060895

Serum 5-Hydroxyindoleacetic Acid and Ratio of 5-Hydroxyindoleacetic Acid to Serotonin as Metabolomics Indicators for Acute Oxidative Stress and Inflammation in Vancomycin-Associated Acute Kidney Injury

Lee¹, HS; Kim, SM; Jang, JH; Park, HD; Lee, SY

ANN LAB MED 2021 10.3343/alm.2021.41.3.268

Immunosuppressive Drug Measurement by Liquid Chromatography Coupled to Tandem Mass Spectrometry: Interlaboratory Comparison in the Korean Clinical Laboratories

Kim¹, HK; Park, HD; Lee, SG; Chae, H; Song, SH; Lee, YW; Yun, YM; Ahn, S; Kim, S; Lee, SM; Lee, SY; Chun, S

CLIN CHEM LAB MED 2021 10.1515/cclm-2020-1392

Prognostic implication of elevated cardiac troponin I in patients visiting emergency department without diagnosis of coronary artery disease

Song¹, M; Kim, T; Kang, EJ; Park, JE; Park, SH; Cha, WC; Yoon, H; Hwang, SY; Shin, TG; Sim, MS; Jo, I; Park, HD; Choi, JH

ANN LAB MED 2021 10.3343/alm.2021.41.2.230

Schemes and Performance Evaluation Criteria of Korean Association of External Quality Assessment (KEQAS) for Improving Laboratory Testing

Kim¹, S; Lee, K; Park, HD; Lee, YW; Chun, S; Min, WK

DRUG DES DEVEL THER 2021 10.2147/DDDT.S285488

Individualized Vancomycin Dosing with Therapeutic Drug Monitoring and Pharmacokinetic Consultation Service: A Large-Scale Retrospective Observational Study

Kim¹, SM; Lee, HS; Hwang, NY; Kim, K; Park, HD; Lee, SY

ARCH PATHOL LAB MED 2021 10.5858/arpa.2020-0112-RA

Current Status of Clinical Application of Point-of-Care Testing

Park¹, HD

ANN LAB MED 2021 10.3343/alm.2021.41.1.114

Comparison of Three Blood Collection Tubes for 35 Biochemical Analytes: The Becton Dickinson Barricor Tube, Serum Separating Tube, and Plasma Separating Tube

Shin¹, S; Oh, J; Park, HD

J KOREAN MED SCI 2020 10.3346/jkms.2020.35.e376

Therapeutic Drug Level Monitoring of Teicoplanin in Korean Pediatric Patients with Normal versus Impaired Renal Function

Choi¹, JS; Kim, JM; Kim, D; Kim, SH; Cho, H; Park, HD; Lee, SY; Kang, CI; Kim, YJ

CLIN CARDIOL 2020 10.1002/clc.23486

Cardiac troponin I predicts clinical outcome of patients with cancer at emergency department

Park¹, S; Kim, T; Cha, WC; Yoon, H; Hwang, SY; Shin, TG; Sim, MS; Jo, I; Lee, SH; Park, HD; Choi, JH

ANN LAB MED 2019 10.3343/alm.2019.39.5.447

Use of Liquid Chromatography-Tandem Mass Spectrometry for Clinical Testing in Korean Laboratories: a Questionnaire Survey

Chae¹, H; Cho, SE; Park, HD; Chun, S; Lee, YW; Yun, YM; Song, SH; Lee, SG; Lee, K; Song, J; Lee, SY

J CLIN LAB ANAL 2019 10.1002/jcla.22921

Performance evaluation of serum PIVKA-II measurement using HISCL-5000 and a method comparison of HISCL-5000, LUMIPULSE G1200, and ARCHITECT i2000

Ryu¹, MR; Kang, ES; Park, HD

INFECT DRUG RESIST 2019 10.2147/IDR.S208783

A nationwide utilization survey of therapeutic drug monitoring for five antibiotics in South Korea

Choi¹, R; Woo, HI; Park, HD; Lee, SY

BMC NEPHROLOGY 2019 10.1186/s12882-019-1403-1

Creatinine- and cystatin C-based estimated glomerular filtration rate slopes for the prediction of kidney outcome: a comparative retrospective study

Kim¹, S; Hwang, S; Jang, HR; Sohn, I; Ahn, HS; Park, HD; Huh, W; Jin, DC; Kim, YG; Kim, DJ; Oh, HY; Lee, JE

J TRACE ELEM MED BIO 2019 10.1016/j.jtemb.2019.02.004

Assessment of 7 trace elements in serum of patients with nontuberculous mycobacterial lung disease

Oh¹, J; Shin, SH; Choi, R; Kim, S; Park, HD; Kim, SY; Han, SA; Koh, WJ; Lee, SY

J PHARMACEUT BIOMED 2019 10.1016/j.jpba.2019.02.001

Therapeutic drug monitoring of teicoplanin using an LC-MS/MS method: Analysis of 421 measurements in a naturalistic clinical setting

Jung¹, J; Lee, K; Oh, J; Choi, R; Woo, HI; Park, HD; Kang, CI; Kim, YJ; Lee, SY

NUTRIENTS 2019 10.3390/nu11030668

Reply: "Letter to the Editor Re: Oh J., et al. Nutrients 2019, 11, 343"

Oh¹, J; Park, HD; Kim, SY; Koh, WJ; Lee, SY

ANN LAB MED 2019 10.3343/alm.2019.39.3.243

Accurate and Rapid Measurement of Glycated Hemoglobin Using HLC-723 G11 Variant Mode

Park¹, MS; Lee, K; Song, J; Park, HD

ANN LAB MED 2019 10.3343/alm.2019.39.3.269

Dried Blood Spot Multiplexed Steroid Profiling Using Liquid Chromatography Tandem Mass Spectrometry in Korean Neonates

Choi¹, R; Park, HD; Oh, HJ; Lee, K; Song, J; Lee, SY

NUTRIENTS 2019 10.3390/nu11020343

Assessment of Vitamin Status in Patients with Nontuberculous Mycobacterial Pulmonary Disease: Potential Role of Vitamin A as a Risk Factor

Oh¹, J; Park, HD; Kim, SY; Koh, WJ; Lee, SY

ANN CLIN LAB SCI 2018

Rare Association of Mucolipidosis III alpha/beta with Dilated Cardiomyopathy

Kwak¹, MJ; Lee, HW; Kim, YM; Cho, SY; Park, HD; Jin, DK

ANN LAB MED 2018 10.3343/alm.2018.38.6.530

Clinical Utility and Cross-Reactivity of Insulin and C-Peptide Assays by the Lumipulse G1200 System

Oh¹, J; Kim, JH; Park, HD

SCAND J CLIN LAB INV 2018 10.1080/00365513.2018.1502464

Performance evaluation of serum IgG subclass quantification using a SPAPLUS turbidimetric analyzer and comparison with the BNII nephelometer

Cho¹, EH; Choi, R; Kang, ES; Park, HD

J PEDIATR ENDOCR MET 2017 10.1515/jpem-2017-0158

Reassessing the significance of the PAH c.158G > A (p.Arg53His) variant in patients with hyperphenylalaninemia

Choi¹, R; Lee, J; Park, HD; Park, JE; Kim, YH; Ki, CS; Lee, SY; Song, J; Kim, JW; Lee, DH

Ann Lab Med. 2017 May;37(3):261-266. doi: 10.3343/alm.2017.37.3.261.

Novel SLC37A4 Mutations in Korean Patients With Glycogen Storage Disease lb

Choi R1¹, Park HD2, Ko JM3, Lee J4, Lee DH4, Hong SJ5, Ki CS1, Lee SY1, Kim JW1, Song J6, Choe YH7.

J Infect. 2017 Mar;74(3):272-280. doi: 10.1016/j.jinf.2016.10.009. Epub 2016 Nov 10.

Evaluation of vitamin status in patients with pulmonary tuberculosis

Oh J1¹, Choi R1, Park HD1, Lee H2, Jeong BH2, Park HY2, Jeon K2, Kwon OJ2, Koh WJ3, Lee SY4.

Ann Lab Med. 2017 Mar;37(2):169-171. doi: 10.3343/alm.2017.37.2.169.

Thyroxine (T4) Autoantibody Interference of Free T4 Concentration Measurement in a Patient With Hashimoto's Thyroiditis

Lee MN1¹, Lee SY2, Hur KY3, Park HD4.

Gut. 2017 Feb;66(2):323-329. doi: 10.1136/gutjnl-2016-311854. Epub 2016 Sep 6.

Non-alcoholic fatty liver disease and progression of coronary artery calcium score: a retrospective cohort study

Sinn DH1¹, Kang D2, Chang Y3,4,5, Ryu S3,4,5, Gu S6, Kim H6, Seong D2, Cho SJ7, Yi BK2,8, Park HD9, Paik SW1, Song YB1,10, Lazo M10, Lima JA10, Guallar E10, Cho J2,3,5,10, Gwak GY1.

ANNALS OF LABORATORY MEDICINE, JAN 2017, 37(1):58-62, DOI: 10.3343/alm.2017.37.1.58

Novel Pathogenic Variant (c.580C>7) in the CPS1 Gene in a Newborn With Carbamoyl Phosphate Synthetase 1 Deficiency Identified by Whole Exome Sequencing

Choi R¹, Park HD, Yang M, Ki CS, Lee SY, Kim JW, Song J, Chang YS, Park WS

Ann Lab Med. 2017 Jan;37(1):63-65. doi: 10.3343/alm.2017.37.1.63.

First Report of Familial Dysalbuminemic Hyperthyroxinemia With an ALB Variant

Cho YY1¹,2, Song JS3, Park HD3, Kim YN1, Kim HI1, Kim TH1, Chung JH1, Ki CS4, Kim SW5.

Ann Lab Med. 2016 Mar;36(2):145-53. doi: 10.3343/alm.2016.36.2.145.

DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population

Park KJ1¹, Park HK2, Kim YJ2, Lee KR2, Park JH1, Park JH3, Park HD4, Lee SY4, Kim JW1,5.

Ann Lab Med. 2016 Nov;36(6):561-72. doi: 10.3343/alm.2016.36.6.561.

A Population-Based Genomic Study of Inherited Metabolic Diseases Detected Through Newborn Screening

Park KJ1¹, Park S2, Lee E2, Park JH1, Park JH3, Park HD4, Lee SY4, Kim JW1,5.

Ann Lab Med. 2016 Sep;36(5):413-9. doi: 10.3343/alm.2016.36.5.413.

Performance Evaluation of the Serum Thyroglobulin Assays With Immunochemiluminometric Assay and Immunoradiometric Assay for Differentiated Thyroid Cancer

Cho YY1¹, Chun S2, Lee SY2, Chung JH1, Park HD3, Kim SW4.

Eur J Intern Med. 2016 Sep;33:88-92. doi: 10.1016/j.ejim.2016.06.028. Epub 2016 Jul 12.

Diagnostic performances of M-protein tests according to the clinical presentations of kidney disease

Koo EH1¹, Shin JH1, Jang HR1, Park HD2, Kwon GY3, Huh W1, Kim DJ1, Kim YG1, Oh HY1, Lee JE4.

BMC Med Genet. 2016 Aug 12;17(1):58. doi: 10.1186/s12881-016-0319-x.

Report of 5 novel mutations of the alpha-L-iduronidase gene and comparison of Korean mutations in relation with those of Japan or China in patients with mucopolysaccharidosis I

Kwak MJ1¹, Huh R2, Kim J2, Park HD3, Cho SY2, Jin DK4.

Clin Biochem. 2016 May;49(7-8):573-9. doi: 10.1016/j.clinbiochem.2016.01.010. Epub 2016 Jan 15.

A simple and rapid analytical method based on solid-phase extraction and liquid chromatography-tandem mass spectrometry for the simultaneous determination of free catecholamines and metanephrines in urine and its application to routine clinical analysis

Woo HI1¹, Yang JS2, Oh HJ3, Cho YY4, Kim JH4, Park HD3, Lee SY5.

BMC Med Genet. 2016 Apr 21;17:33. doi: 10.1186/s12881-016-0295-1.

PHKA2 mutation spectrum in Korean patients with glycogen storage disease type IX: prevalence of deletion mutations

Choi R1¹, Park HD2, Kang B3, Choi SY3, Ki CS1, Lee SY1, Kim JW1, Song J4, Choe YH5.

Clin Biochem. 2015 Dec;48(18):1350-3. doi: 10.1016/j.clinbiochem.2015.08.016. Epub 2015 Aug 18.

Direct assay of iduronate-2-sulfatase for Hunter disease using UPLC-tandem mass spectrometry and fluorogenic substrate

Lee K1¹, Jun SH2, Song SH3, Park HD4, Park KU1, Song J5.

Ann Lab Med. 2015 Nov;35(6):578-85. doi: 10.3343/alm.2015.35.6.578.

Dried Blood Spot Testing for Seven Steroids Using Liquid Chromatography-Tandem Mass Spectrometry With Reference Interval Determination in the Korean Population

Kim B1¹, Lee MN1, Park HD1, Kim JW1, Chang YS2, Park WS2, Lee SY3.

J Anal Toxicol. 2015 Nov-Dec;39(9):675-85. doi: 10.1093/jat/bkv057. Epub 2015 Aug 3.

Comparison of Different Time of Flight-Mass Spectrometry Modes for Small Molecule Quantitative Analysis

Chindarkar NS1¹, Park HD2, Stone JA1, Fitzgerald RL1.

Ann Hepatol. 2015 Nov-Dec;14(6):882-8. doi: 10.5604/16652681.1171776.

Evaluation of alpha-fetoprotein as a screening marker for hepatocellular carcinoma in hepatitis prevalent areas

Chun S1¹, Rhie SY2, Ki CS1, Kim JE2, Park HD1.

Ann Lab Med. 2015 Sep;35(5):535-9. doi: 10.3343/alm.2015.35.5.535.

CYP21A2 Mutation Analysis in Korean Patients With Congenital Adrenal Hyperplasia Using Complementary Methods: Sequencing After Long-Range PCR and Restriction Fragment Length Polymorphism Analysis With Multiple Ligation-Dependent Probe Amplification Assay

Hong G1¹, Park HD2, Choi R1, Jin DK3, Kim JH4, Ki CS1, Lee SY1, Song J5, Kim JW1.

Ann Lab Med. 2015 Sep;35(5):519-22. doi: 10.3343/alm.2015.35.5.519.

Development and Validation of Liquid Chromatography-Tandem Mass Spectrometry Method for Quantification of Plasma Metanephrines for Differential Diagnosis of Adrenal Incidentaloma

Lee SM1¹, Lee MN1,2, Oh HJ1, Cho YY3, Kim JH3, Woo HI4, Park HD1, Lee SY5.

Ann Lab Med. 2015 Jul;35(4):458-62. doi: 10.3343/alm.2015.35.4.458. Epub 2015 May 21.

Biochemical and Genetic Analysis of Seven Korean Individuals With Suspected Metachromatic Leukodystrophy

Han M1¹, Jun SH2, Lee YJ3, Eun BL4, Lee SJ1, Seong MW1, Park SS1, Song SH1, Park HD5, Song J6.

Clin Chim Acta. 2015 Apr 15;444:50-3. doi: 10.1016/j.cca.2015.02.008. Epub 2015 Feb 11.

Application of whole exome sequencing to a rare inherited metabolic disease with neurological and gastrointestinal manifestations: A congenital disorder of glycosylation mimicking glycogen storage disease

Choi R1¹, Woo HI2, Choe BH3, Park S4, Yoon Y4, Ki CS1, Lee SY1, Kim JW1, Song J5, Kim DS6, Kwon S6, Park HD7.

Transplant Proc. 2015 Mar;47(2):504-10. doi: 10.1016/j.transproceed.2014.10.049.

Usefulness of High-Sensitivity Troponin I for the Monitoring of Subclinical Acute Cellular Rejection After Cardiac Transplantation

Ahn KT1¹, Choi JO1, Lee GY1, Park HD2, Jeon ES3.

Ann Clin Lab Sci. 2015 Spring;45(2):152-7.

The Distribution of Abbott High-Sensitivity Troponin I Levels in Korean Patients with Chest Pain

Lee K1¹, Lee SY1, Choi JO2, Jeon ES2, Park HD3.

Clin Genet. 2015 Feb;87(2):196-8. doi: 10.1111/cge.12350. Epub 2014 Feb 21.

A novel ACAD8 mutation in asymptomatic patients with isobutyryl-CoA dehydrogenase deficiency and a review of the ACAD8 mutation spectrum

Yun JW1¹, Jo KI, Woo HI, Lee SY, Ki CS, Kim JW, Song J, Lee DH, Lee YW, Park HD.

Ann Lab Med. 2015 Jan;35(1):41-9. doi: 10.3343/alm.2015.35.1.41. Epub 2014 Dec 8.

A Simple and Rapid Method Based on Liquid Chromatography-Tandem Mass Spectrometry for the Measurement of alpha-L-Iduronidase Activity in Dried Blood Spots: An Application to Mucopolysaccharidosis I (Hurler) Screening

Yang JS1¹, Min HK1, Oh HJ2, Woo HI3, Lee SY4, Kim JW3, Song J5, Park HD3.

Ann Lab Med. 2015 Jan;35(1):165-8. doi: 10.3343/alm.2015.35.1.165. Epub 2014 Dec 8.

Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry Measurement of Leukocyte Arylsulfatase A Activity Using a Natural Substrate

Han M1¹, Jun SH2, Song SH1, Park HD3, Park KU4, Song J4.

Diabetes Metab. 2014 Sep;40(4):272-7. doi: 10.1016/j.diabet.2014.01.006. Epub 2014 Mar 11.

Strong correlation between glycaemic variability and total glucose exposure in type 2 diabetes is limited to subjects with satisfactory glycaemic control

Suh S1¹, Joung JY2, Jin SM2, Kim MY2, Bae JC2, Park HD3, Lee MS2, Lee MK2, Kim JH4.

Ann Clin Lab Sci. 2014 Spring;44(2):213-6.

A Korean Patient with Glutaric Aciduria Type 1 with a Novel Mutation in the Glutaryl CoA Dehydrogenase Gene

Kim HS1¹, Yu HJ, Lee J, Park HD, Kim JH, Shin HJ, Jin DK, Lee M.

J Perinat Med. 2014 Jan;42(1):121-7. doi: 10.1515/jpm-2013-0154.

Steroid profiling for congenital adrenal hyperplasia by tandem mass spectrometry as a second-tier test reduces follow-up burdens in a tertiary care hospital: A retrospective and prospective evaluation

Seo JY¹, Park HD, Kim JW, Oh HJ, Yang JS, Chang YS, Park WS, Lee SY.

J Anal Toxicol. 2014 Sep;38(7):387-96. doi: 10.1093/jat/bku075. Epub 2014 Jul 1.

False-Positive Interferences of Common Urine Drug Screen Immunoassays: A Review

Saitman A1¹, Park HD2, Fitzgerald RL3.

BMC Med Genet. 2014 Aug 15;15:94. doi: 10.1186/s12881-014-0094-5.

Novel GALT variations and mutation spectrum in the Korean population with decreased galactose-1-phosphate uridyltransferase activity

Choi R¹, Jo KI, Ko DH, Lee DH, Song J, Jin DK, Ki CS, Lee SY, Kim JW, Lee YW1, Park HD.

Choi HJ1, Bang HI2, Ki CS1, Lee SY1, Kim JW1, Song J3, Shin MR4, Lee YW5, Lee DH6, Park HD7.

Two Novel FAH Gene Mutations in a Patient with Hereditary Tyrosinemia Type I

Choi HJ1¹, Bang HI2, Ki CS1, Lee SY1, Kim JW1, Song J3, Shin MR4, Lee YW5, Lee DH6, Park HD7.

Clin Chim Acta. 2014 Apr 20;431:1-8. doi: 10.1016/j.cca.2014.01.032. Epub 2014 Feb 5.

Molecular genetics of citrullinemia types I and II

Woo HI1¹, Park HD2, Lee YW3.

Rapid Commun Mass Spectrom. 2014 Mar 30;28(6):587-94. doi: 10.1002/rcm.6823.

Ultra-performance liquid chromatography/tandem mass spectrometry for determination of sulfatides in dried blood spots from patients with metachromatic leukodystrophy

Han M1¹, Jun SH, Song SH, Park HD, Park KU, Song J.

Clin Chem Lab Med. 2013 Nov;51(11):2195-200. doi: 10.1515/cclm-2013-0045.

The relationship between estimated average glucose and fasting plasma glucose

Kim HY¹, Lee SY, Suh S, Kim JH, Lee MK, Park HD.

Clin Chem Lab Med. 2013 Aug;51(8):e179-82. doi: 10.1515/cclm-2012-0737.

Establishing reference intervals for LDL subfractions in a Korean population using the Lipoprint LDL system

Huh HJ¹, Park BT, Lee SY, Kang ES, Park HD.

Ann Clin Lab Sci. 2013 Summer;43(3):311-6.

Three Patients with Glycogen Storage Disease Type II and the Mutational Spectrum of GAA in Korean Patients

Park HD1¹, Lee DH, Choi TY, Lee YK, Lee SY, Kim JW, Ki CS, Lee YW.

A Novel Mutation (c.200T > C) in the NAGLU Gene of a Korean Patient with Mucopolysaccharidosis IIIB

A Novel Mutation (c.200T > C) in the NAGLU Gene of a Korean Patient with Mucopolysaccharidosis IIIB

¹,A Novel Mutation (c.200T > C) in the NAGLU Gene of a Korean Patient with Mucopolysaccharidosis IIIB

Am J Med Genet A. 2013 Mar;161A(3):509-17. doi: 10.1002/ajmg.a.35298. Epub 2013 Feb 8.

Five novel mutations of GALNS in Korean patients with mucopolysaccharidosis IVA

Park HD1¹, Ko AR, Ki CS, Lee SY, Kim JW, Cho SY, Kim SH, Park SW, Sohn YB, Jin DK.

Clin Biochem. 2013 Feb;46(3):209-13. doi: 10.1016/j.clinbiochem.2012.10.008. Epub 2012 Oct 22.

Mutation spectrum of the ASS1 gene in Korean patients with citrullinemia type I

Woo HI1¹, Ki CS, Lee SY, Kim JW, Song J, Jin DK, Park WS, Lee DH, Lee YW, Park HD.

Ann Lab Med. 2013 Jan;33(1):75-9. doi: 10.3343/alm.2013.33.1.75. Epub 2012 Dec 17.

The First Korean Case of Mucopolysaccharidosis IIIC (Sanfilippo Syndrome Type C) Confirmed by Biochemical and Molecular Investigation

Huh HJ1¹, Seo JY, Cho SY, Ki CS, Lee SY, Kim JW, Park HD, Jin DK.

Ann Clin Lab Sci. 2013 Winter;43(1):31-6.

Identification of PRODH Mutations in Korean Neonates with Type 1 Hyperprolinemia

Jang MA1¹, Kim BC, Ki CS, Lee SY, Kim JW, Choi TY, Lee DH, Song J, Lee YW, Park HD.

Proteomics.?2012 Dec;12(23-24):3590-7. doi: 10.1002/pmic.201200101.

Serum CA19-9, cathepsin D, and matrix metalloproteinase-7 as a diagnostic panel for pancreatic ductal adenocarcinoma

Park HD1¹,?Kang ES,?Kim JW,?Lee KT,?Lee KH,?Park YS,?Park JO,?Lee J,?Heo JS,?Choi SH,?Choi DW,?Kim S,?Lee JK,?Lee SY.

Ann Clin Lab Sci. 2012 Fall;42(4):424-8.

SLC22A5 Mutations in a Patient with Systemic Primary Carnitine Deficiency: The First Korean Case Confirmed by Biochemical and Molecular Investigation

Yoon YA1¹, Lee DH, Ki CS, Lee SY, Kim JW, Lee YW, Park HD.

Genet Med. 2012 Jul;14(7):648-55. doi: 10.1038/gim.2012.2. Epub 2012 Feb 16.

Enhanced interpretation of newborn screening results without analyte cutoff values

Marquardt G¹, Currier R, McHugh DM, Gavrilov D, Magera MJ, Matern D, Oglesbee D, Raymond K, Rinaldo P, Smith EH, Tortorelli S, Turgeon CT, Lorey F, Wilcken B, Wiley V, Greed LC, Lewis B, Boemer F, Schoos R, Marie S, Vincent MF, Sica YC, Domingos MT, Al-Thihli K, Sinclair G, Al-Dirbashi OY, Chakraborty P, Dymerski M, Porter C, Manning A, Seashore MR, Quesada J, Reuben A, Chrastina P, Hornik P, Atef Mandour I, Atty Sharaf SA, Bodamer O, Dy B, Torres J, Zori R, Cheillan D, Vianey-Saban C, Ludvigson D, Stembridge A, Bonham J, Downing M, Dotsikas Y, Loukas YL, Papakonstantinou V, Zacharioudakis GS, Bar?th ?, Karg E, Franzson L, Jonsson JJ, Breen NN, Lesko BG, Berberich SL, Turner K, Ruoppolo M, Scolamiero E, Antonozzi I, Carducci C, Caruso U, Cassanello M, la Marca G, Pasquini E, Di Gangi IM, Giordano G, Camilot M, Teofoli F, Manos SM, Peterson CK, Mayfield Gibson SK, Sevier DW, Lee SY, Park HD, Khneisser I, Browning P, Gulamali-Majid F, Watson MS, Eaton RB, Sahai I, Ruiz C, Torres R, Seeterlin MA, Stanley EL, Hietala A, McCann M, Campbell C, Hopkins PV, de Sain-Van der Velden MG, Elvers B, Morrissey MA, Sunny S, Knoll D, Webster D, Frazier DM, McClure JD, Sesser DE, Willis SA, Rocha H, Vilarinho L, John C, Lim J, Caldwell SG, Tomashitis K, Casti?eiras Ramos DE, Cocho de Juan JA, Rueda Fern?ndez I, Yahyaoui Mac?as R, Egea-Mellado JM, Gonz?lez-Gallego I, Delgado Pecellin C, Garc?a-Valdecasas Bermejo MS, Chien YH, Hwu WL, Childs T, McKeever CD, Tanyalcin T, Abdulrahman M, Queijo C, Lemes A, Davis T, Hoffman W, Baker M, Hoffman GL.

J Korean Acad Nurs. 2012 Jun;42(3):443-51. doi: 10.4040/jkan.2012.42.3.443.

A Comparison of the Rates of Hemolysis and Repeated Blood Sampling using Syringe Needles versus Vacuum Tube Needles in the Emergency Department

Sung YH1¹, Hwang MS, Lee JH, Park HD, Ryu KH, Cho MS, Yi YH, Song S.

Ann Hematol. 2012 Apr;91(4):511-7. doi: 10.1007/s00277-011-1326-9. Epub 2011 Sep 8.

Gene mutations in the Ras pathway and the prognostic implication in Korean patients with juvenile myelomonocytic leukemia

Park HD1¹, Lee SH, Sung KW, Koo HH, Jung NG, Cho B, Kim HK, Park IA, Lee KO, Ki CS, Kim SH, Yoo KH, Kim HJ.

Ann Clin Lab Sci. 2012 Winter;42(1):7-13.

The Relationship between Serum Neutrophil Gelatinase-Associated Lipocalin and Renal Function in Patients with Vancomycin Treatment

Park HD1¹, Seo JY, Lee SY.

Clin Genet. 2012 Jan;81(1):96-8. doi: 10.1111/j.1399-0004.2011.01704.x.

Mutational spectrum in eight Korean patients with 3-methylcrotonyl-CoA carboxylase deficiency

Cho SY¹, Park HD, Lee YW, Ki CS, Lee SY, Sohn YB, Park SW, Kim SH, Ji S, Kim SJ, Choi EW, Kim CH, Ko AR, Paik KH, Lee DH, Jin DK.

Ann Clin Lab Sci. 2011 Spring;41(2):197-200.

A novel PHKA2 gross deletion mutation in a Korean patient with X-linked liver glycogenosis type I

Park KJ1¹, Park HD, Lee SY, Ki CS, Choe YH.

Ann Clin Lab Sci. 2011 Spring;41(2):167-73.

Three Korean Patients with Maple Syrup Urine Disease: Four Novel Mutations in the BCKDHA Gene

Park HD1¹, Lee DH, Hong YH, Kang DH, Lee YK, Song J, Lee SY, Kim JW, Ki CS, Lee YW.

Genet Med. 2011 Mar;13(3):230-54. doi: 10.1097/GIM.0b013e31820d5e67.

Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: A worldwide collaborative project

McHugh D¹, Cameron CA, Abdenur JE, Abdulrahman M, Adair O, Al Nuaimi SA, ?hlman H, Allen JJ, Antonozzi I, Archer S, Au S, Auray-Blais C, Baker M, Bamforth F, Beckmann K, Pino GB, Berberich SL, Binard R, Boemer F, Bonham J, Breen NN, Bryant SC, Caggana M, Caldwell SG, Camilot M, Campbell C, Carducci C, Bryant SC, Caggana M, Caldwell SG, Camilot M, Campbell C, Carducci C, Cariappa R, Carlisle C, Caruso U, Cassanello M, Castilla AM, Ramos DE, Chakraborty P, Chandrasekar R, Ramos AC, Cheillan D, Chien YH, Childs TA, Chrastina P, Sica YC, de Juan JA, Colandre ME, Espinoza VC, Corso G, Currier R, Cyr D, Czuczy N, D'Apolito O, Davis T, de Sain-Van der Velden MG, Delgado Pecellin C, Di Gangi IM, Di Stefano CM, Dotsikas Y, Downing M, Downs SM, Dy B, Dymerski M, Rueda I, Elvers B, Eaton R, Eckerd BM, El Mougy F, Eroh S, Espada M, Evans C, Fawbush S, Fijolek KF, Fisher L, Franzson L, Frazier DM, Garcia LR, Bermejo MS, Gavrilov D, Gerace R, Giordano G, Irazabal YG, Greed LC, Grier R, Grycki E, Gu X, Gulamali-Majid F, Hagar AF, Han L, Hannon WH, Haslip C, Hassan FA, He M, Hietala A, Himstedt L, Hoffman GL, Hoffman W, Hoggatt P, Hopkins PV, Hougaard DM, Hughes K, Hunt PR, Hwu WL, Hynes J, Ibarra-Gonz?lez I, Ingham CA, Ivanova M, Jacox WB, John C, Johnson JP, J?nsson JJ, Karg E, Kasper D, Klopper B, Katakouzinos D, Khneisser I, Knoll D, Kobayashi H, Koneski R, Kozich V, Kouapei R, Kohlmueller D, Kremensky I, la Marca G, Lavochkin M, Lee SY, Lehotay DC, Lemes A, Lepage J, Lesko B, Lewis B, Lim C, Linard S, Lindner M, Lloyd-Puryear MA, Lorey F, Loukas YL, Luedtke J, Maffitt N, Magee JF, Manning A, Manos S, Marie S, Hadachi SM, Marquardt G, Martin SJ, Matern D, Mayfield Gibson SK, Mayne P, McCallister TD, McCann M, McClure J, McGill JJ, McKeever CD, McNeilly B, Morrissey MA, Moutsatsou P, Mulcahy EA, Nikoloudis D, Norgaard-Pedersen B, Oglesbee D, Oltarzewski M, Ombrone D, Ojodu J, Papakonstantinou V, Reoyo SP, Park HD, Pasquali M, Pasquini E, Patel P, Pass KA, Peterson C, Pettersen RD, Pitt JJ, Poh S, Pollak A, Porter C, Poston PA, Price RW, Queijo C, Quesada J, Randell E, Ranieri E, Raymond K, Reddic JE, Reuben A, Ricciardi C, Rinaldo P, Rivera JD, Roberts A, Rocha H, Roche G, Greenberg CR, Mellado JM, Juan-Fita MJ, Ruiz C, Ruoppolo M, Rutledge SL, Ryu E, Saban C, Sahai I, Garc?a-Blanco MI, Santiago-Borrero P, Schenone A, Schoos R, Schweitzer B, Scott P, Seashore MR, Seeterlin MA, Sesser DE, Sevier DW, Shone SM, Sinclair G, Skrinska VA, Stanley EL, Strovel ET, Jones AL, Sunny S, Takats Z, Tanyalcin T, Teofoli F, Thompson JR, Tomashitis K, Domingos MT, Torres J, Torres R, Tortorelli S, Turi S, Turner K, Tzanakos N, Valiente AG, Vallance H, Vela-Amieva M, Vilarinho L, von D?beln U, Vincent MF, Vorster BC, Watson MS, Webster D, Weiss S, Wilcken B, Wiley V, Williams SK, Willis SA, Woontner M, Wright K, Yahyaoui R, Yamaguchi S, Yssel M, Zakowicz WM.

Ann Clin Lab Sci. 2011 Fall;41(1):44-7.

Brief Communication: Multiplex Ligation-Dependent Probe Amplification Assay for Diagnosis of Congenital Adrenal Hyperplasia

¹,Brief Communication: Multiplex Ligation-Dependent Probe Amplification Assay for Diagnosis of Congenital Adrenal Hyperplasia

Korean J Lab Med. 2011 Jan;31(1):54-60. doi: 10.3343/kjlm.2011.31.1.54.

Clinical, Biochemical and Genetic Analyses in Two Korean Patients with Medium-chain Acyl-CoA Dehydrogenase Deficiency

Woo HI1¹, Park HD, Lee YW, Lee DH, Ki CS, Lee SY, Kim JW.

Ann Clin Lab Sci. 2010 Summer;40(3):261-6.

Clinical, Biochemical, and Genetic Analysis of Korean Patients with Pseudohypoparathyroidism Type Ia

Park CH1¹, Park HD, Lee SY, Kim JW, Sohn YB, Park SW, Jin DK.

Clin Chem. 2010 May;56(5):764-71. doi: 10.1373/clinchem.2009.139618. Epub 2010 Mar 18.

Multiplex Enzyme Assay for Galactosemia Using Ultraperformance Liquid Chromatography-Tandem Mass Spectrometry

Ko DH1¹, Jun SH, Park HD, Song SH, Park KU, Kim JQ, Song YH, Song J.

J Obstet Gynaecol. 2009 Nov;29(8):694-7. doi: 10.3109/01443610903177128.

Acitretin-contaminated blood products and pregnancy

Han JY1¹, Choi JS, Chun JM, Park HD, Lee SY, Kim CH, Park Q, Nava-Ocampo AA, Koren G.

Korean J Lab Med. 2010 Feb;30(1):51-7. doi: 10.3343/kjlm.2010.30.1.51.

The Relationship between Lewis/Secretor Genotypes and Serum Carbohydrate Antigen 19-9 Levels in a Korean Population

Park HD1¹, Park KU, Song J, Ki CS, Han KS, Kim JQ.

Ann Clin Lab Sci. 2010 Winter;40(1):15-9.

Association of ATP7B Mutation Detection Rate with Biochemical Characteristics in Korean Patients with Wilson Disease

Park HD1¹, Park HK, Chung HS, Lee SY, Kim JW, Ki CS.

Ann Clin Lab Sci. 2010 Winter;40(1):20-5.

Clinical and Genetic Analysis of Korean Patients with Cornelia de Lange Syndrome: Two Novel NIPBL Mutations

Park HD1¹, Ki CS, Kim JW, Kim WT, Kim JK.

J Obstet Gynaecol. 2009 Nov;29(8):694-7. doi: 10.3109/01443610903177128.

Pregnancy outcome of women transfused during pregnancy with blood products inadvertently obtained from donors treated with acitretin

Han JY1¹, Choi JS, Chun JM, Park HD, Lee SY, Kim CH, Park Q, Nava-Ocampo AA, Koren G.

Ann Clin Lab Sci. 2009 Fall;39(4):399-404.

Two Novel HADHB Gene Mutations in a Korean Patient with Mitochondrial Trifunctional Protein Deficiency

Park HD1¹, Kim SR, Ki CS, Lee SY, Chang YS, Jin DK, Park WS.

Clin Chem Lab Med. 2009;47(8):930-3. doi: 10.1515/CCLM.2009.223.

Clinical, biochemical, and genetic analysis of a Korean neonate with hereditary tyrosinemia type 1

Park HD1¹, Lee DH, Choi TY, Lee YK, Kim JW, Ki CS, Lee YW.

Int J Clin Pharmacol Ther. 2009 Jul;47(7):476-82.

A fully validated HPLC method for the simultaneous determination of acitretin and etretinate in plasma and its application to a pharmacokinetic study in healthy Korean subjects

Park HD1¹, Kim HK, Chun MR, Kim JW, Kim DW, Lee JH, Huh WS, Youn JI, Kim HG, Kim YG, Kim MH, Lee SY.

Cancer Genet Cytogenet. 2009 Jul 15;192(2):90-2. doi: 10.1016/j.cancergencyto.2009.03.013.

A novel four-way t(6;16;21;8)(p21.3;p11.2;q22;q22) in acute myeloid leukemia with RUNX1/RUNX1T1 rearrangement

Park KJ¹, Park HD, Kim HJ, Yoo KH, Koo HH, Kim SH.

Clin Genet. 2009 Apr;75(4):405-7. doi: 10.1111/j.1399-0004.2008.01132.x.

Carrier frequency of the R778L, A874V, and N1270S mutations in the ATP7B gene in a Korean population

Carrier frequency of the R778L¹, A874V, and N1270S mutations in the ATP7B gene in a Korean population

BMC Med Genet. 2009 Mar 24;10:29. doi: 10.1186/1471-2350-10-29.

A novel c.-22T > C mutation in GALK1 promoter is associated with elevated galactokinase phenotype

Park HD1¹, Kim YK, Park KU, Kim JQ, Song YH, Song J.

Ann Clin Lab Sci. 2009 Spring;39(2):188-91.

A Novel ATP7A Gross Deletion Mutation in a Korean Patient with Menkes Disease

Park HD1¹, Moon HK, Lee J, Lee M, Lee SY, Kim JW, Ki CS.

Transfusion. 2008 Nov;48(11):2395-400. doi: 10.1111/j.1537-2995.2008.01850.x. Epub 2008 Jul 22.

Evaluation of the transfusion safety of blood products and determination of plasma concentrations of acitretin and etretinate in patients receiving transfusions

Park HD1¹, Kim HK, Kim JW, Kim DW, Lee JH, Huh W, Youn JI, Kim HG, Kim YG, Kim MH, Lee SY.