Publications by authors named "Rimm Huh"

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Prevalence of idiopathic scoliosis in girls with central precocious puberty: effect of a gonadotropin-releasing hormone agonist.
Lindsey Yoojin Chung, Hyo-Kyoung Nam, Young-Jun Rhie, Rimm Huh, Kee-Hyoung Lee

Ann Pediatr Endocrinol Metab· June 2020

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Late-onset noninfectious interstitial lung disease following autologous haematopoietic stem cell transplantation in paediatric patients.
Yoon-Kyoung Lee, Rimm Huh, Jihyun Kim, Kangmo Ahn, Ki Woong Sung

Respirology· August 2016

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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.
Min Jung Kwak, Rimm Huh, Jinsup Kim, Hyung-Doo Park, Sung Yoon Cho

BMC Med Genet· August 2016

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Letter to the Editor: A Novel Mutation in the CREBBP Gene of a Korean Girl with Rubinstein-Taybi syndrome.
Rimm Huh, Sung Yoon Cho, Jinsup Kim, Chang-Seok Ki, Dong-Kyu Jin

Ann Clin Lab Sci· May 2016

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First Korean Case of Infantile Hypophosphatasia with Novel Mutation in ALPL and Literature Review.
Eu Gene Park, Sung Yoon Cho, Jeehun Lee, Jihyun Kim, Heeyeon Cho, Rimm Huh

Ann Clin Lab Sci· May 2016

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Estrogen-mediated Height Control in Girls with Marfan Syndrome.
Dong-Yun Lee, Hye Sun Hyun, Rimm Huh, Dong-Kyu Jin, Duk-Kyung Kim

J Korean Med Sci· February 2016

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Hypoparathyroidism in a 3-year-old Korean boy with Sotos syndrome and a novel mutation in NSD1.
Karn Wejaphikul, Sung Yoon Cho, Rimm Huh, Younghee Kwun, Jieun Lee

Ann Clin Lab Sci· January 2016

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A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia.
Mi Sun Chang, Jong Chul Han, Jieun Lee, Younghee Kwun, Rimm Huh

Ann Clin Lab Sci· December 2015

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Pharmacokinetics, Pharmacodynamics, and Efficacy of a Novel Long-Acting Human Growth Hormone: Fc Fusion Protein.
Su Jin Kim, Hyun-Hee Kwak, Sung Yoon Cho, Young Bae Sohn, Sung Won Park, Rimm Huh

Mol Pharm· October 2015

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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.
Hyeseon Kim, Jinsup Kim, Rimm Huh, Sung Yoon Cho, Dong-Kyu Jin

Ann Pediatr Endocrinol Metab· June 2015

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Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion.
Aram Yang, Yeon Hee Lee, Soon Young Nam, Yu Ju Jeong, Yechan Kyung, Rimm Huh

Ann Pediatr Endocrinol Metab· March 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.
Young Bae Sohn, Sung Yoon Cho, Jieun Lee, Yonghee Kwun, Rimm Huh

Mol Genet Metab· February 2015

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Identification and in vivo functional characterization of novel compound heterozygous BMP1 variants in osteogenesis imperfecta.
Sung Yoon Cho, P V Asharani, Ok-Hwa Kim, Aritoshi Iida, Noriko Miyake, Rimm Huh

Hum Mutat· February 2015

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Disease-specific growth charts for Korean infants with Prader-Willi syndrome.
Jieun Lee, Tsuyoshi Isojima, Mi Sun Chang, Young Hee Kwun, Rimm Huh

Am J Med Genet A· January 2015

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Impact of enzyme replacement therapy on linear growth in Korean patients with mucopolysaccharidosis type II (Hunter syndrome).
Sung Yoon Cho, Rimm Huh, Mi Sun Chang, Jieun Lee, Younghee Kwun

J Korean Med Sci· February 2014

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