Publications by authors named "Mi Sun Chang"

Claim this Profile
A
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, Chang-Seok Ki, Changwon Kee

Ann Clin Lab Sci· December 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Osteogenesis imperfecta Type I caused by a novel mutation in the start codon of the COL1A1 gene in a Korean family.
Sung Yoon Cho, Ji-Ho Lee, Chang-Seok Ki, Mi Sun Chang, Dong-Kyu Jin

Ann Clin Lab Sci· December 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Disease-specific Growth Charts of Marfan Syndrome Patients in Korea.
Younghee Kwun, Su Jin Kim, Jieun Lee, Tsuyoshi Isojima, Doo-Seok Choi, MiSun Chang

J Korean Med Sci· July 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
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

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Improvement of cardiac function by short-term enzyme replacement therapy in a murine model of cardiomyopathy associated with Hunter syndrome evaluated by serial echocardiography with speckle tracking 2-D strain analysis.
Sang-Chol Lee, Jieun Lee, Dong-Kyu Jin, Jung-Sun Kim, Eun-Seok Jeon, Mi Sun Chang

Mol Genet Metab· July 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A biochemical and physicochemical comparison of two recombinant enzymes used for enzyme replacement therapies of hunter syndrome.
Yo Kyung Chung, Young Bae Sohn, Jong Mun Sohn, Jieun Lee, Mi Sun Chang

Glycoconj J· May 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
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

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center.
Yangho Yoo, Mi Sun Chang, Jieun Lee, Sung Yoon Cho, Sung Won Park

Ann Pediatr Endocrinol Metab· September 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis