Rimm Huh
Seoul, Republic of Korea
Last Updated: 09/26/2026
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Found 16 publications
Prevalence of idiopathic scoliosis in girls with central precocious puberty: effect of a gonadotropin-releasing hormone agonist.
Journal: Annals of pediatric endocrinology & metabolism
Published: October 07, 2019
First Korean Case of Infantile Hypophosphatasia with Novel Mutation in ALPL and Literature Review.
Journal: Annals of clinical and laboratory science
Published: June 18, 2016
Pharmacokinetics, Pharmacodynamics, and Efficacy of a Novel Long-Acting Human Growth Hormone: Fc Fusion Protein.
Journal: Molecular pharmaceutics
Published: September 16, 2015
Estrogen-mediated Height Control in Girls with Marfan Syndrome.
Journal: Journal of Korean medical science
Published: September 10, 2015
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.
Journal: BMC medical genetics
Published: September 07, 2015
Letter to the Editor: A Novel Mutation in the CREBBP Gene of a Korean Girl with Rubinstein-Taybi syndrome.
Journal: Annals of clinical and laboratory science
Published: August 16, 2015
Late-onset noninfectious interstitial lung disease following autologous haematopoietic stem cell transplantation in paediatric patients.
Journal: Respirology (Carlton, Vic.)
Published: August 08, 2015
Elevation of serum creatine kinase during methimazole treatment of Graves disease in a 13-year-old girl and a literature review of similar cases.
Journal: Annals of pediatric endocrinology & metabolism
Published: May 18, 2015
Hypoparathyroidism in a 3-year-old Korean boy with Sotos syndrome and a novel mutation in NSD1.
Journal: Annals of clinical and laboratory science
Published: April 19, 2015
A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia.
Journal: Annals of clinical and laboratory science
Published: February 20, 2015
Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion.
Journal: Annals of pediatric endocrinology & metabolism
Published: September 29, 2014
Safety and efficacy of enzyme replacement therapy with idursulfase beta in children aged younger than 6 years with Hunter syndrome.
Journal: Molecular genetics and metabolism
Published: July 08, 2014
Last Updated: 09/26/2026