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American Journal of Medical Genetics. Part A|March 27, 2013
Improvement of CNS defects via continuous intrathecal enzyme replacement by osmotic pump in mucopolysaccharidosis type II miceYoung Bae Sohn, Jeehun Lee, Sung Yoon Cho, et al.
Scientific Reports|November 9, 2019
Impact of BMI on peak growth hormone responses to provocative tests and therapeutic outcome in children with growth hormone deficiencyAram Yang, Sung Yoon Cho, Min Jung Kwak, et al.
Medicine|February 23, 2023
Six-year clinical outcomes of enzyme replacement therapy for perinatal lethal and infantile hypophosphatasia in Korea: Two case reportsInsung Kim, Eu-Seon Noh, Min-Sun Kim, et al.
Medicine|May 24, 2024
Cartilage-hair hypoplasia-anauxetic dysplasia spectrum disorders harboring RMRP mutations in two Korean children: A case reportJu Heon Park, Minji Im, Yae-Jean Kim, et al.
Annals of Clinical and Laboratory Science|June 28, 2015
Spinal Stenosis with Paraparesis in a Korean Boy with Albright's Hereditary Osteodystrophy: Identification of a Novel Nonsense Mutation in the GNASSang Heon Lee, Seung Hyeon Mun, Sung Yoon Cho, et al.
Annals of Pediatric Endocrinology & Metabolism|October 20, 2021
Wilson disease diagnosed incidentally by targeted gene panel sequencing in a Korean boy with severe obesityMinji Im, Ari Song, Jiyeon Kim, et al.
American Journal of Medical Genetics. Part A|October 24, 2014
Disease-specific growth charts for Korean infants with Prader-Willi syndromeJieun Lee, Tsuyoshi Isojima, Mi Sun Chang, et al.
International Journal of Molecular Sciences|January 21, 2023
WT1 Pulsed Human CD141+ Dendritic Cell Vaccine Has High Potential in Solid Tumor-Targeted ImmunotherapySung Yoon Cho, Seong Mun Jeong, Young Joo Jeon, et al.
Orphanet Journal of Rare Diseases|September 27, 2015
Decreased performance in IDUA knockout mouse mimic limitations of joint function and locomotion in patients with Hurler syndromeChihwa Kim, Min Jung Kwak, Sung Yoon Cho, et al.
Journal of Human Genetics|January 11, 2013
The proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in KoreaSung Yoon Cho, Chang-Seok Ki, Young Bae Sohn, et al.
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