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Prevalence of idiopathic scoliosis in girls with central precocious puberty: effect of a gonadotropin-releasing hormone agonist

Annals of Pediatric Endocrinology & Metabolism, 2020, 25(2), , pp.92-96

2020

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Elevation of serum creatine kinase during methimazole treatment of Graves disease in a 13-year-old girl and a literature review of similar cases

Annals of Pediatric Endocrinology & Metabolism, 2015, 20(2), , pp.106-109

2015

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Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion

Annals of Pediatric Endocrinology & Metabolism, 2015, 20(1), , pp.40-45

2015

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Safety and efficacy of enzyme replacement therapy with idursulfase beta in children aged younger than 6 years with Hunter syndrome

Molecular genetics and metabolism, 2015-02, Vol.114 (2), p.156-160

2015

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

BMC medical genetics, 2016-08, Vol.17 (1), p.58-58, Article 58

2016

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Safety and efficacy of enzyme replacement therapy with idursulfase beta in children aged younger than 6years with Hunter syndrome

Molecular genetics and metabolism, 2015-02, Vol.114 (2), p.156-160

2015

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

Molecular pharmaceutics, 2015-10, Vol.12 (10), p.3759-3765

2015

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Late-onset noninfectious interstitial lung disease following autologous haematopoietic stem cell transplantation in paediatric patients

Respirology (Carlton, Vic.), 2016-08, Vol.21 (6), p.1068-1074

2016

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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

BMC medical genetics, 2016-08, Vol.17 (1)

2016

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Identification and In Vivo Functional Characterization of Novel Compound Heterozygous BMP1 Variants in Osteogenesis Imperfecta

Human mutation, 2015-02, Vol.36 (2), p.191-195

2015

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Disease-specific growth charts for Korean infants with Prader-Willi syndrome

American journal of medical genetics. Part A, 2015-01, Vol.167A (1), p.86-94

2015

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Letter to the Editor: A Novel Mutation in the CREBBP Gene of a Korean Girl with Rubinstein-Taybi syndrome

Annals of clinical and laboratory science, 2015, Vol.45 (4), p.458

2015

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Estrogen-mediated Height Control in Girls with Marfan Syndrome

Journal of Korean Medical Science, 2016, 31(2), 211, pp.275-279

2016

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First Korean Case of Infantile Hypophosphatasia with Novel Mutation in ALPL and Literature Review

Annals of clinical and laboratory science, 2016-05, Vol.46 (3), p.302-307

2016

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Hypoparathyroidism in a 3-year-old Korean boy with Sotos syndrome and a novel mutation in NSD1

Annals of clinical and laboratory science, 2015, Vol.45 (2), p.215-218

2015

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A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia

Annals of clinical and laboratory science, 2015, Vol.45 (1), p.90-93

2015

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Impact of enzyme replacement therapy on linear growth in Korean patients with mucopolysaccharidosis type II (Hunter syndrome)

Journal of Korean Medical Science, 2014, 29(2), 185, pp.254-260

2014

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Letter to the Editor: A Novel Mutation in the CREBBP Gene of a Korean Girl with Rubinstein-Taybi syndrome

Annals of clinical and laboratory science, 2015, Vol.45 (4), p.458-461

2015

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Glycogen Storage Disease Presenting as Fetal Hydrops: A Case Report

Korean Journal of Perinatology, 2013, Vol.24 (3), p.187

2013

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Prevalence of idiopathic scoliosis in girls with central precocious puberty: effect of a gonadotropin-releasing hormone agonist

Elevation of serum creatine kinase during methimazole treatment of Graves disease in a 13-year-old girl and a literature review of similar cases

Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion

Safety and efficacy of enzyme replacement therapy with idursulfase beta in children aged younger than 6 years with Hunter syndrome

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

Safety and efficacy of enzyme replacement therapy with idursulfase beta in children aged younger than 6years with Hunter syndrome

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

Late-onset noninfectious interstitial lung disease following autologous haematopoietic stem cell transplantation in paediatric patients

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

Identification and In Vivo Functional Characterization of Novel Compound Heterozygous BMP1 Variants in Osteogenesis Imperfecta

Disease-specific growth charts for Korean infants with Prader-Willi syndrome

Letter to the Editor: A Novel Mutation in the CREBBP Gene of a Korean Girl with Rubinstein-Taybi syndrome

Estrogen-mediated Height Control in Girls with Marfan Syndrome

First Korean Case of Infantile Hypophosphatasia with Novel Mutation in ALPL and Literature Review

Hypoparathyroidism in a 3-year-old Korean boy with Sotos syndrome and a novel mutation in NSD1

A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia

Impact of enzyme replacement therapy on linear growth in Korean patients with mucopolysaccharidosis type II (Hunter syndrome)

Letter to the Editor: A Novel Mutation in the CREBBP Gene of a Korean Girl with Rubinstein-Taybi syndrome

Glycogen Storage Disease Presenting as Fetal Hydrops: A Case Report

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