Genetic obesity: an update with emerging therapeutic approaches

por Sohn, Young Bae
Publicado 2022

Updates on Paget’s Disease of Bone

por Choi, Yong Jun, Sohn, Young Bae, Chung, Yoon-Sok
Publicado 2022

The First Korean Patient with Potocki-Shaffer Syndrome: A Rare Cause of Multiple Exostoses

por Sohn, Young Bae, Yim, Shin-Young, Cho, Eun-Hae, Kim, Ok-Hwa
Publicado 2015

Reciprocal Deletion and Duplication of 17p11.2-11.2: Korean Patients with Smith-Magenis Syndrome and Potocki-Lupski Syndrome

por Lee, Cha Gon, Park, Sang-Jin, Yun, Jun-No, Yim, Shin-Young, Sohn, Young Bae
Publicado 2012

An Unusual Presentation of Diabetic Ketoacidosis in Familial Hajdu-Cheney Syndrome: A Case Report

por Lee, Gil-Ho, An, So-Yeon, Sohn, Young Bae, Jeong, Seon-Yong, Chung, Yoon-Sok
Publicado 2013

A case report of pycnodysostosis with atypical femur fracture diagnosed by next-generation sequencing of candidate genes

por Song, Hyung Keun, Sohn, Young Bae, Choi, Yong Jun, Chung, Yoon-Sok, Jang, Ja-Hyun
Publicado 2017

Rare presentation of Rothmund-Thomson syndrome with predominantly cutaneous findings

por Yang, Ji Young, Sohn, Young Bae, Lee, Jin-Sung, Jang, Ja-Hyun, Lee, Eun-So
Publicado 2017

Successful switching from insulin to sulfonylurea in a 3-month-old infant with diabetes due to p.G53D mutation in KCNJ11

por Yoon, Jong Seo, Park, Kyu Jung, Sohn, Young Bae, Lee, Hae Sang, Hwang, Jin Soon
Publicado 2018

Design and rationale for a comparison study of Olmesartan and Valsartan On myocardial metabolism In patients with Dilated cardiomyopathy (OVOID) trial: study protocol for a randomi...

por Jo, Sua, Moon, Hyeyeon, Park, Kyungil, Sohn, Chang-Bae, Kim, Jeonghwan, Kwon, Yong-Seop, Kim, Su Hong
Publicado 2022

Osteogenesis Imperfecta Type VI with Severe Bony Deformities Caused by Novel Compound Heterozygous Mutations in SERPINF1

por Cho, Sung Yoon, Ki, Chang-Seok, Sohn, Young Bae, Kim, Su Jin, Maeng, Se Hyun, Jin, Dong-Kyu
Publicado 2013

A Case of CATCH22 Syndrome Diagnosed in Postmenopausal Woman

por Lee, Seung Kyung, Lee, Min Jeong, Lee, Hyo Jin, Kim, Bu Kyung, Sohn, Young Bae, Chung, Yoon-Sok
Publicado 2013

Serum levels of FGF21 are reduced and negatively correlated with adiponectin in children with Prader-Willi syndrome

por Kim, Su Jin, Sohn, Young Bae, Cho, Sung-Yoon, Choi, Young Ok, Kim, Chi Hwa, Jin, Dong-Kyu
Publicado 2013

Effects of recombinant human growth hormone treatment on growth, body composition, and safety in infants or toddlers with Prader-Willi syndrome: a randomized, active-controlled tri...

por Yang, Aram, Choi, Jin-Ho, Sohn, Young Bae, Eom, Yunae, Lee, Jiyoon, Yoo, Han-Wook, Jin, Dong-Kyu
Publicado 2019

When do we need more than local compression to control intraoral haemorrhage?

por Sohn, Jun-Bae, Lee, Ho, Han, Yoon-Sic, Jung, Da-Un, Sim, Hye-Young, Kim, Hee-Sun, Oh, Sohee
Publicado 2019

Impact of Scoring Balloon Angioplasty on Lesion Preparation for DCB Treatment of Coronary Lesions

por Shin, Eun-Seok, Ann, Soe Hee, Jang, Mi Hee, Kim, Bitna, Kim, Tae-Hyun, Sohn, Chang-Bae, Choi, Byung Joo
Publicado 2023

Array-Based Comparative Genomic Hybridization in 190 Korean Patients with Developmental Delay and/or Intellectual Disability: A Single Tertiary Care University Center Study

por Lee, Cha Gon, Park, Sang-Jin, Yun, Jun-No, Ko, Jung Min, Kim, Hyon-Ju, Yim, Shin-Young, Sohn, Young Bae
Publicado 2013

Fracture patterns and causes in the craniofacial region: an 8-year review of 2076 patients

por Jin, Ki-Su, Lee, Ho, Sohn, Jun-Bae, Han, Yoon-Sic, Jung, Da-Un, Sim, Hye-Young, Kim, Hee-Sun
Publicado 2018

A novel MLL2 gene mutation in a Korean patient with Kabuki syndrome

por Kim, Soo Jin, Cho, Sung Yoon, Maeng, Se Hyun, Sohn, Young Bae, Kim, Su-Jin, Ki, Chang-Seok, Jin, Dong-Kyu
Publicado 2013

Network analysis of the metabolome and transcriptome reveals novel regulation of potato pigmentation

por Cho, Kyoungwon, Cho, Kwang-Soo, Sohn, Hwang-Bae, Ha, In Jin, Hong, Su-Young, Lee, Hyerim, Kim, Young-Mi, Nam, Myung Hee
Publicado 2016

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

por Cho, Sung Yoon, Lee, Jeehun, Ko, Ah-Ra, Kwak, Min Jung, Kim, Sujin, Sohn, Young Bae, Park, Sung Won, Jin, Dong-Kyu
Publicado 2015