Park HD - Search Results

1

Two novel HADHB gene mutations in a Korean patient with mitochondrial trifunctional protein deficiency.

Park HD, Kim SR, Ki CS, Lee SY, Chang YS, Jin DK, Park WS. Park HD, et al. Among authors: park ws. Ann Clin Lab Sci. 2009 Fall;39(4):399-404. Ann Clin Lab Sci. 2009. PMID: 19880769

2

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

Park HD, Kim HK, Kim JW, Kim DW, Lee JH, Huh W, Youn JI, Kim HG, Kim YG, Kim MH, Lee SY. Park HD, et al. Transfusion. 2008 Nov;48(11):2395-400. doi: 10.1111/j.1537-2995.2008.01850.x. Epub 2008 Jul 22. Transfusion. 2008. PMID: 18657077

3

Biochemical and molecular investigation of two Korean patients with glycogen storage disease type III.

Oh SH, Park HD, Ki CS, Choe YH, Lee SY. Oh SH, et al. Among authors: park hd. Clin Chem Lab Med. 2008;46(9):1245-9. doi: 10.1515/CCLM.2008.252. Clin Chem Lab Med. 2008. PMID: 18785866

4

A novel ATP7A gross deletion mutation in a Korean patient with Menkes disease.

Park HD, Moon HK, Lee J, Lee M, Lee SY, Kim JW, Ki CS. Park HD, et al. Ann Clin Lab Sci. 2009 Spring;39(2):188-91. Ann Clin Lab Sci. 2009. PMID: 19429807

5

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

Park HD, Lee DH, Choi TY, Lee YK, Kim JW, Ki CS, Lee YW. Park HD, et al. Clin Chem Lab Med. 2009;47(8):930-3. doi: 10.1515/CCLM.2009.223. Clin Chem Lab Med. 2009. PMID: 19569981

6

Association of ATP7B mutation detection rate with biochemical characteristics in Korean patients with Wilson disease.

Park HD, Park HK, Chung HS, Lee SY, Kim JW, Ki CS. Park HD, et al. Among authors: park hk. Ann Clin Lab Sci. 2010 Winter;40(1):15-9. Ann Clin Lab Sci. 2010. PMID: 20124325

7

Clinical and genetic analysis of Korean patients with Cornelia de Lange syndrome: two novel NIPBL mutations.

Park HD, Ki CS, Kim JW, Kim WT, Kim JK. Park HD, et al. Ann Clin Lab Sci. 2010 Winter;40(1):20-5. Ann Clin Lab Sci. 2010. PMID: 20124326

8

The relationship between Lewis/Secretor genotypes and serum carbohydrate antigen 19-9 levels in a Korean population.

Park HD, Park KU, Song J, Ki CS, Han KS, Kim JQ. Park HD, et al. Among authors: park ku. Korean J Lab Med. 2010 Feb;30(1):51-7. doi: 10.3343/kjlm.2010.30.1.51. Korean J Lab Med. 2010. PMID: 20197723

9

Clinical, biochemical, and genetic analysis of korean patients with pseudohypoparathyroidism type Ia.

Park CH, Park HD, Lee SY, Kim JW, Sohn YB, Park SW, Jin DK. Park CH, et al. Among authors: park hd, park sw. Ann Clin Lab Sci. 2010 Summer;40(3):261-6. Ann Clin Lab Sci. 2010. PMID: 20689139

10

A mother and daughter with the p.R443X mutation of mucopolysaccharidosis type II: Genotype and phenotype analysis.

Sohn YB, Kim SJ, Park SW, Park HD, Ki CS, Kim CH, Huh SW, Yeau S, Paik KH, Jin DK. Sohn YB, et al. Among authors: park hd, park sw. Am J Med Genet A. 2010 Dec;152A(12):3129-32. doi: 10.1002/ajmg.a.33589. Am J Med Genet A. 2010. PMID: 21108396

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