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

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

Publikováno v: Annals of Pediatric Endocrinology & Metabolism, Vol 20, Iss 2, Pp 106-109 (2015)

We report a 13-year-old girl with Graves disease, who showed an increased level of serum creatine kinase (CK) accompanied by myalgia after methimazole (MMI) treatment. This patient developed muscular pain two weeks after MMI administration, along wit

Externí odkaz: https://doaj.org/article/57fbe40cc5f34f9fb20c5979ab5d0f1c

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

Autor: Hyo Kyoung Nam, Lindsey Yoojin Chung, Rimm Huh, Kee Hyoung Lee, Young Jun Rhie

Publikováno v: Annals of Pediatric Endocrinology & Metabolism
Annals of Pediatric Endocrinology & Metabolism, Vol 25, Iss 2, Pp 92-96 (2020)

Purpose Adolescent idiopathic scoliosis (AIS) is the most common form of scoliosis and occurs in children between 10 to 18 years old, during periods of growth spurts and puberty changes. In patients with central precocious puberty (CPP), due to early

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7a9267032fa35f1eec8d163161f0236
http://europepmc.org/articles/PMC7336263

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

Autor: Ki Woong Sung, Yoon-Kyoung Lee, Kangmo Ahn, Jihyun Kim, Rimm Huh, Joongbum Cho

Publikováno v: Respirology. 21:1068-1074

Background and objective High-dose chemotherapy (HDCT) followed by autologous haematopoietic stem cell transplantation (HSCT) is widely used in paediatric cancer patients, but few data about noninfectious interstitial lung disease (ILD) following thi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cc3e358536806f667dd95d3e0c72454c
https://doi.org/10.1111/resp.12787

Comment on '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'

Autor: Sung Yoon Cho, Jinsup Kim, Dong-Kyu Jin, Min Jung Kwak, Rimm Huh, Hyung-Doo Park

Publikováno v: Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-2 (2018)
BMC Medical Genetics

Background Mucopolysaccharidosis I (MPS I) is an autosomal recessive lysosomal storage disorder caused by a lack of the lysosomal enzyme α-L-iduronidase (IDUA). To date, more than 200 IDUA mutations have been reported. However, only a few types of m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de3f1bafce3945bd389ff56dc2591b12

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

Autor: Sung Yoon Cho, Young Bae Sohn, Rimm Huh, Jieun Lee, Dong-Kyu Jin, Yonghee Kwun

Publikováno v: Molecular Genetics and Metabolism. 114:156-160

Idursulfase beta (Hunterase®) has been used for enzyme replacement therapy (ERT) of patients with mucopolysaccharidosis II (MPS II, Hunter syndrome) aged 6 years or older since 2012 in Korea. The objective of this study was to evaluate the safety an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f12f86af4785bf3fd0f4cb71e54fc5f3
https://doi.org/10.1016/j.ymgme.2014.08.009