60.

임신 출산 육아 대백과 - 제일병원 저 (박성원 공저) ,

비타북스, 2017/04/01



59. 

헌터 환자 길라잡이

58. 

Article Increase of Prevalence of Obesity and Metabolic Syndrome in Children and Adolescents in Korea during the COVID-19 Pandemic: A Cross-Sectional Study Using the KNHANES . 

Jung Eun Choi 1, Hye Ah Lee 2, Sung Won Park 3, Jung Won Lee, Ji Hyen Lee 1, Hyesook Park 4, Hae Soon Kim 1

Children 2023 Jun 23;10(7):1105.

57. 

"Hyponatremia in children with respiratory infections: a cross-sectional analysis of a cohort of 3938 patients.

Park, Sung Won, et al.

Scientific reports 8.1 (2018): 16494.

56. 

Hyponatremia in children with respiratory infections: a cross-sectional analysis of a cohort of 3938 patients Sung Won Park1, Son Moon Shin 1,MoonsunJeong1 ,Dong-Hee Cho2 , Keum Hwa Lee3, Michael Eisenhut4 ,

Sci Rep. 2018 Nov 7;8(1):164-94

55. 

Use of child safety seats during transportation of newborns.

김선혁, 박성원, 이연경, 고선영, 신손문*.

Korean J Pediatr. 2018 Aug;61(8):253-7.

54. 

Clinical Experiences with Febrile Infants, Younger than Three Months, with Urinary Tract Infection in a Single Center for Four Years: Incidence, Pathogens and Viral Co-infections.

윤석호, 신손문, 박성원*.

Child Kidney Dis. 2017 Oct;21(2):101-6.

53. 

Maternal food restrictions during breastfeeding.

정고운, 박성원, 이연경, 고선영, 신손문*.

Korean J Pediatr. 2017 Mar;60(3):70-6.

52

영아의 부모들에게 권장할 적절한 체온 측정 방법.

명관대, 박성원, 정고운, 이희철, 윤소영, 신손문*.

J Korean Soc Emerg Med. 2016 Oct;27(5):458-63. Korean.

51. 

단일기관에서 이중 질량 분석법(tandem mass spectrometry technology)을 이용한 선천성 대사이상 검사의 위양성율에 대한 연구.

김현수, 신손문, 고선영, 이연경, 박성원*.

J Korean Soc Inher Metab Dis. 2016 Apr; 16(1):18-23. Korean.

50. 

Predicting Factors of Roseola Infantum Infected with Human Herpesvirus 6 from Urinary Tract Infection.

고홍렬, 신손문, 박성원*.

Child Kidney Dis 2016 Oct; 20(2): 69-73.

49. 

Novel and Recurrent ACADS Mutations and Clinical Manifestations Observed in Korean Patients with Short-chain Acyl-coenzyme a Dehydrogenase Deficiency. Kim YM, Cheon CK*, Park KH, 

박성원, Kim GH, Yoo HW, Lee KA, Ko JM*. Ann Clin Lab Sci. 2016 Jul;46(4):360-6.

48. 

A new case of turner syndrome with early pubertal development.

윤석호, 이동준, 신손문, 윤소영, 박성원*.

Int J Clin Med. 2016 May;7(5):342-6.

47. 

The Prenatal and Postnatal Incidence of Congenital Anomalies of the Kidneys and Urinary Tract (CAKUT) Detected by Ultrasound.

최현아, 이동준, 신손문, 이연경, 고선영, 박성원*.

Child Kidney Dis. 2016 Apr;20(1):29-32. English.

46. 

AAV8-mediated expression of N-acetylglucosamine-1-phosphate transferase attenuates bone loss in a mouse model of mucolipidosis II.

Ko AR, Jin DK*, Cho SY, 박성원, Przybylska M, Yew NS, Cheng SH, Kim JS, Kwak MJ, Kim SJ, Sohn YB.

Mol Genet Metab. 2016 Apr;117(4):447-55.

45.

A Case of Short-chain Acyl-CoA Dehydrogenase Deficiency Detected by Newborn Screening.

박경원, Ko JM, 정고운, 이희철, 윤소영, 고선영, 이연경, 신손문, 박성원*.

J Korean Soc Inherit Metab Dis 2015 Apr;15(1):40-3.

44. 

Disease-specific Growth Charts of Marfan Syndrome Patients in Korea. Kwun Y, Kim SJ, Lee J, Isojima T, Choi DS, Kim DK, Huh J, Kang IS, Chang M, Cho SY, Sohn YB, 박성원, Jin DK*.

J Korean Med Sci. 2015 Jul;30(7):911-6.

43. 

Pharmacokinetics, Pharmacodynamics, and Efficacy of a Novel Long-Acting Human Growth Hormone: Fc Fusion Protein.

Kim SJ, Kwak HH, Cho SY, Sohn YB, 박성원, Huh R, Kim J, Ko AR, Jin DK*.

Mol Pharm. 2015 Oct 5;12(10):3759-65.

42. 

Effect of systemic high dose enzyme replacement therapy on the improvement of CNS defects in a mouse model of mucopolysaccharidosis type II.

Cho SY, Lee J, Ko AR, Kwak MJ, Kim S, Sohn YB, 박성원, Jin DK*.

Orphanet J Rare Dis. 2015 Oct 31;10:141.

41. 

Case of mild Schmid-type metaphyseal chondrodysplasia with novel sequence variation involving an unusual mutational site of the COL10A1 gene.

Park H, Hong S, Cho SI, Kim OH, Cho TJ, Choi IH, Jin DK, Sohn YB, 박성원, Cho HH, Cheon JE, Kim SY, Kim JY, Park SS, Seong MW*.

Eur J Med Genet. 2015 Mar;58(3):175-9.

40. 

Identification and in vivo functional characterization of novel compound heterozygous BMP1 variants in osteogenesis imperfecta.

Cho SY, Asharani PV, Kim OH, Iida A, Miyake N, Matsumoto N, Nishimura G, Ki CS, Hong G, Kim SJ, Sohn YB, 박성원, Lee J, Kwun Y, Carney TJ, Huh R, Ikegawa S*, Jin DK*.

Hum Mutat. 2015 Feb;36(2):191-5.

39. 

Amiodarone으로 태아 빈맥 치료 후 출생한 미숙아 환아에서 생후 1개월에 발현된 상심실성 빈맥과 일과성 갑상샘 기능이상의 경험

남승우, 고선영*, 이연경, 윤소영, 박성원, 신손문.

Korean J Perinatol. 2014 Sep;25(3):189-194. Korean.

38. 

Impact of Enzyme Replacement Therapy on Linear Growth in Korean Patients with Mucopolysaccharidosis Type II (Hunter Syndrome).

Cho SY, Huh R, Chang MS, Lee J, Kwun Y, Maeng SH, Kim SJ, Sohn YB, 박성원, Kwon EK, Han SJ, Jung J, Jin DK*.

J Korean Med Sci. 2014 Feb;29(2):254-60.

37. 

Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center.

Yoo Y, Chang MS, Lee J, Cho SY, 박성원, Jin DK*, Park HD.

Ann Pediatr Endocrinol Metab. 2013 Sep;18(3):128-34. English.

36. 

Five novel mutations of GALNS in Korean patients with mucopolysaccharidosis IVA.

Park HD, Ko AR, Ki CS, Lee SY, Kim JW, Cho SY, Kim SH, 박성원, Sohn YB, Jin DK*.

Am J Med Genet A. 2013 Mar;161A(3):509-17.

35. 

모유수유 지속여부가 모유황달 치료 및 모유수유 성공에 미치는 영향.

안은섭, 김민균, 이연경, 고선영, 윤소영, 정고운, 박성원, 신손문*.

Korean J Perinatol. 2013 Dec;24(4):259-64. Korean.

34. 

Another possible underlying mechanism for the positive association between celiac disease and systemic lupus erythematosus: the role of interleukin 21.

박성원, Park SJ, Shin JI*.

J Rheumatol. 2013 Sep;40(9):1619.

33. 

Phase I/II clinical trial of enzyme replacement therapy with idursulfase beta in patients with mucopolysaccharidosis II (Hunter Syndrome).

Sohn YB, Cho SY, 박성원, Kim SJ, Ko AR, Kwon EK, Han SJ, Jin DK*.

Orphanet J Rare Dis. 2013 Mar 18;8:42.

32. 

Diagnosis and constitutional and laboratory features of Korean girls referred for precocious puberty.

Kim D, Cho SY, Maeng SH, Yi ES, Jung YJ, 박성원, Sohn YB, Jin DK*

Korean J Pediatr. 2012 Dec;55(12):481-6. English.

31. 

Identification of 11 novel mutations in 49 Korean patients with mucopolysaccharidosis type II.

Sohn YB, Ki CS, Kim CH, Ko AR, Yook YJ, Lee SJ, Kim SJ, 박성원, Yeau S, Kwon EK, Han SJ, Choi EW, Lee SY, Kim JW, Jin DK.

Clin Genet. 2012 Feb;81(2):185-90.

30. 

Retrospective analysis of the clinical manifestations and survival of Korean patients with mucopolysaccharidosis type II: Emphasis on the cardiovascular complication and mortality cases.

Sohn YB, Choi EW, Kim SJ, 박성원, Kim SH, Cho SY, Jeong SI, Huh J, Kang IS, Lee HJ, Paik KH, Jin DK. 

Am J Med Genet A. 2012 Jan;158A(1):90-6.

29. 

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

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

Clin Genet. 2012 Jan;81(1):96-8.

28. 

A Korean patient with Morquio B disease with a novel c.13_14insA mutation in the GLB1 gene.

Sohn YB, Park HD, 박성원, Kim SH, Cho SY, Ko AR, Ki CS, Yeau S, Jin DK.

Ann Clin Lab Sci. 2012 Winter;42(1):89-93.

27. 

A study of the relationship between clinical phenotypes and plasma iduronate-2-sulfatase enzyme activities in Hunter syndrome patients.

Lee OJ, Kim SJ, Sohn YB, Park HD, Lee SY, Kim CH, Ko AR, Yook YJ, Lee SJ, 박성원, Kim SH, Cho SY, Kwon EK, Han SJ, Jin DK.

Korean J Pediatr. 2012 Mar;55(3):88-92. English.

26. 

Enzyme replacement therapy improves joint motion and outcome of the 12-min walk test in a mucopolysaccharidosis type VI patient previously treated with bone marrow transplantation.

Sohn YB, 박성원, Kim SH, Cho SY, Ji ST, Kwon EK, Han SJ, Oh SJ, Park YJ, Ko AR, Paik KH, Lee J, Lee DH, Jin DK.

Am J Med Genet A. 2012 May;158A(5):1158-63.

25. 

Two novel insulin receptor gene mutations in a patient with Rabson-Mendenhall syndrome: the first Korean case confirmed by biochemical, and molecular evidence.

Kim D, Cho SY, Yeau SH, 박성원, Sohn YB, Kwon MJ, Kim JY, Ki CS, Jin DK.

J Korean Med Sci. 2012 May;27(5):565-8.

24. 

Familial Xp22.33-Xp22.12 deletion delineated by chromosomal microarray analysis causes proportionate short stature.

Cho SY, Ki CS, Jang JH, Sohn YB, 박성원, Kim SH, Kim SJ, Jin DK.

Am J Med Genet A. 2012 Jun;158A(6):1462-6.

23. 

Auditory characteristics and therapeutic effects of enzyme replacement in mouse model of the mucopolysaccharidosis (MPS) II.

Hong SH, Chu H, Kim KR, Ko MH, Kwon SY, Moon IJ, Chung WH, Cho YS, Kim CH, Suh MW, Choi EW, Sohn YB, 박성원, Kim SH, Cho SY, Ko AR, Jin DK.

Am J Med Genet A. 2012 Sep;158A(9):2131-8.

22. 

Clinical, biochemical, and genetic analysis of two korean patients with trichorhinophalangeal syndrome type I and growth hormone deficiency.

Sohn YB, Ki CS, 박성원, Cho SY, Ko AR, Kwon MJ, Kim JY, Park HD, Kim OH, Jin DK.

Ann Clin Lab Sci. 2012 Summer;42(3):307-12.

21. 

Continuous renal replacement therapy in neonates weighing less than 3 kg.

Sohn YB, Paik KH, Cho HY, Kim SJ, 박성원, Kim ES, Chang YS, Park WS, Choi YH, Jin DK.

Korean J Pediatr. 2012 Aug;55(8):286-92. English.

20. 

LIN28B polymorphisms are associated with central precocious puberty and early puberty in girls.

박성원, Lee ST, Sohn YB, Cho SY, Kim SH, Kim SJ, Kim CH, Ko AR, Paik KH, Kim JW, Jin DK.

Korean J Pediatr. 2012 Oct;55(10):388-92. English.

19. 

Serum cystatin C for estimation of residual renal function in children on peritoneal dialysis.

Kim SJ, Sohn YB, 박성원, Jin DK, Paik KH.

Pediatr Nephrol. 2011 Mar;26(3):433-40.

18. 

Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia.

Kim SJ, Bieganski T, Sohn YB, Kozlowski K, Sem`euml;nov M, Okamoto N, Kim CH, Ko AR, Ahn GH, Choi YL, 박성원, Ki CS, Kim OH, Nishimura G, Unger S, Superti-Furga A, Jin DK.

Hum Genet. 2011 May;129(5):497-502.

17. 

Mutations of ACADS gene associated with short-chain acyl-coenzyme A dehydrogenase deficiency.

Kim SH, Park HD, Sohn YB, 박성원, Cho SY, Ji S, Kim SJ, Choi EW, Kim CH, Ko AR, Yeau S, Paik KH,Jin DK.

Ann Clin Lab Sci. 2011 Fall;41(1):84-8.

16. 

High prevalence of carpal tunnel syndrome in children with mucopolysaccharidosis type II (Hunter syndrome).

Kwon JY, Ko K, Sohn YB, Kim SJ, 박성원, Kim SH, Cho SY, Jin DK.

Am J Med Genet A. 2011 Jun;155A(6):1329-35.

15. 

Two novel PEX1 mutations in a patient with Zellweger syndrome: the first Korean case confirmed by biochemical, and molecular evidence.

Cho SY, Chang YP, Park JY, Park HD, Sohn YB, 박성원, Kim SH, Ji S, Kim SJ, Choi EW, Kim CH, Ko AR, Paik KH, Jin DK.

Ann Clin Lab Sci. 2011 Spring;41(2):182-7.

14. 

The metabolic syndrome and body composition in childhood cancer survivors. Sohn YB, Kim SJ, 박성원, Kim SH, Cho SY, Lee SH, Yoo KH, Sung KW, Chung JH, Koo HH, Jin DK.

Korean J Pediatr. 2011 Jun;54(6):253-9.

13. 

A polymorphism in the growth hormone receptor is associated with height in children with Prader-Willi syndrome.

박성원, Lee ST, Sohn YB, Kim SH, Cho SY, Ko AR, Ji ST, Kwon JY, Yeau S, Paik KH, Kim JW, Jin DK.

Am J Med Genet A. 2011 Dec;155A(12):2970-3.

12. 

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

Park CH, Park HD, Lee SY, Kim JW, Sohn YB, 박성원, Jin DK

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

11. 

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

Sohn YB, Kim SJ, 박성원, Park HD, Ki CS, Kim CH, Huh SW, Yeau S, Paik KH, Jin DK.

Am J Med Genet A. 2010 Dec;152A(12):3129-32.

10. 

A study of early pubertal development and precocious puberty in children with Prader-Willi sydrome. [dissertation]

박성원

서울: 성균관대학교 의과대학 대학원 소아청소년과; 2010년 12월.

9. 

Differential effects of insufflated, subcutaneous, and intravenous growth hormone on bone growth, cognitive function, and NMDA receptor subunit expression.

박성원, Shin S, Kim CH, Ko AR, Kwak MJ, Nam MH, Park SY, Kim SJ, Sohn YB, Galinsky RE, Kim H, Yeo Y, Jin DK.

Endocrinology. 2010 Sep;151(9):4418-27.

8. 

Chronic peritoneal dialysis in a 4-year-old boy with Lesch-Nyhan disease.

Kim SJ, Sohn YB, 박성원, Jin DK, Paik KH.

Pediatr Nephrol. 2009 May;24(5):1089-90.

7. 

Genotyping of CYP21A2 for congenital adrenal hyperplasia screening using allele-specific primer extension followed by bead array hybridization.

6. 

투석 환자에서 성장호르몬 치료의 효과와 성장에 영향을 주는 요인에 대한 연구.

Kim SJ, 박성원, Sohn YB, Jin DK, Paik KH.

J Korean Soc Pediatr Nephrol. 2008 Apr;12(1):38-46. Korean.

5. 

소아 복막 투석 환자에서 발생한 복막염의 경험적 항생제 치료에 관한 연구.

Lee SG, Cho J, Sohn YB, 박성원, Kim SJ, Jin DK, Paik KH.

J Korean Soc Pediatr Nephrol. 2008 Oct;12(2):213-20. Korean.

4. 

중고등학교 교과서에 실린 소아 관련 정보의 조사

김정훈, 박성원, 신손문*, 성인경, 박미정, 정유미, 하정훈

Korean J Pediatr. 2007 Apr;50(4):340-7. Korean.

3. 

증상이 있는 신생아 자발성 기흉에 대한 임상적 연구.

박성원, 윤병호, 김경아, 고선영, 이우길, 신손문, 이연경*

Korean J Perinatol. 2006 Sep;17(3):304-9. Korean.

2. 

자동화 청성뇌간반응을 이용한 신생아 청력선별검사 결과 분석

박성원, 윤병호, 김경아, 고선영, 이연경, 신손문*, 홍성화

Korean J Pediatr. 2006 Oct;49(10):1056-60. Korean.

1.

신생아 황달에서 경피적 빌리루빈 측정기의 유용성

안주란, 박성원, 이희철, 김경아, 고선영, 이연경, 신손문*.

Korean J Pediatr. 2004 Dec;47(12):1287-92. Korean.