Chong Kun Cheon
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Explore the profile of Chong Kun Cheon including associated specialties, affiliations and a list of published articles.
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Articles
67
Citations
401
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Recent Articles
1.
Lee N, Noh H, Cheon C
Stem Cell Res
. 2025 Feb;
84:103690.
PMID: 40020439
Mucopolysaccharidosis Type IIIA (MPS IIIA), known as Sanfilippo syndrome type A, is a rare autosomal recessive lysosomal storage disorder caused by the mutations in the N-sulfoglucosamine Sulfohydrolase (SGSH) gene, encoding...
2.
Lee H, Han J, Jeong R, Kang Y, Choi B, Kim S, et al.
Sci Rep
. 2025 Feb;
15(1):4882.
PMID: 39929944
Mucopolysaccharidosis type II (MPS II) is caused by a deficiency in iduronate-2-sulfatase (Ids), an enzyme that catabolizes glycosaminoglycan (GAG). Ids insufficiency results in the accumulation of GAG in various organs,...
3.
Sung J, Kim I, Im M, Ahn Y, Kim S, Jang J, et al.
Mol Genet Metab Rep
. 2025 Feb;
42:101189.
PMID: 39897469
Mucopolysaccharidosis (MPS) IVA (Morquio A syndrome) is an autosomal recessive lysosomal storage disorder caused by a mutation affecting the enzyme -acetylgalactosamine-6-sulfatase (EC 3.1.6.4, GALNS). Enzyme replacement therapy (ERT) has been...
4.
Jo H, Jang H, Cheon C, Yoon J, Yoo S, Lee J, et al.
BMC Pediatr
. 2025 Feb;
25(1):89.
PMID: 39893395
Background: This study aimed to compare the response to growth hormone (GH) therapy according to the presence of GH deficiency (GHD) in short-stature children born small for gestational age (SGA)...
5.
Lee N, Noh H, Cheon C
Stem Cell Res
. 2025 Jan;
83:103639.
PMID: 39793273
Mucopolysaccharidosis Type Ⅱ, as Known as Hunter syndrome, is a rare X-liked genetic disease caused by mutations in iduronate-2-sulfatase (IDS) gene. We obtained peripheral blood mononuclear cells (PBMCs) from a...
6.
Lee Y, Cheon C, Suh J, Moon J, Ahn M, Chang S, et al.
Ann Pediatr Endocrinol Metab
. 2025 Jan;
29(6):349-355.
PMID: 39778403
Rare endocrine diseases are complex conditions that require lifelong specialized care due to their chronic nature and associated long-term complications. In Korea, a lack of nationwide data on clinical practice...
7.
Cheon C
Ann Pediatr Endocrinol Metab
. 2024 Nov;
29(5):277-278.
PMID: 39506341
No abstract available.
8.
Park J, Choi T, Kim T, Lee Y, Wellalage Don D, George-Abraham J, et al.
J Genet Genomics
. 2024 Oct;
51(12):1389-1403.
PMID: 39368701
Williams syndrome (WS) is a rare multisystemic disorder caused by recurrent microdeletions on 7q11.23, characterized by intellectual disability, distinctive craniofacial and dental features, and cardiovascular problems. Previous studies have explored...
9.
Rivera Romero O, Chae H, Faienza M, Vergani E, Cheon C, Di Mase R, et al.
Front Endocrinol (Lausanne)
. 2024 Jul;
15:1419667.
PMID: 39050564
Introduction: To analyse the perspectives of healthcare professionals (HCPs) regarding the acceptance of digital health solutions for growth hormone (GH) deficiency care. This study identified factors impacting HCPs' intent to...
10.
Lee S, Yoo S, Yoon J, Cheon C, Kim Y
Ann Pediatr Endocrinol Metab
. 2024 Jul;
29(3):207.
PMID: 38956757
No abstract available.