Zobrazeno 1 - 10
of 197
pro vyhledávání: '"Jeong Kee Seo"'
Publikováno v:
Korean Journal of Pediatrics, Vol 58, Iss 1, Pp 28-32 (2015)
PurposeDiencephalic syndrome is an uncommon cause of failure to thrive in early childhood that is associated with central nervous system neoplasms in the hypothalamic-optic chiasmatic region. It is characterized by complex signs and symptoms related
Externí odkaz:
https://doaj.org/article/b15cd70360714ed0ae74ceeb7b5e9f9d
Publikováno v:
Emerging Infectious Diseases, Vol 13, Iss 5, Pp 791-791 (2007)
Externí odkaz:
https://doaj.org/article/671ca0a973984fd696d3a3b10059b69d
Publikováno v:
Journal of Korean Medical Science
Background Glycogen storage disease (GSD) is an inherited disorder leading to abnormal glucose metabolism and glycogen accumulation, and is associated with various complications including hepatic adenoma and hepatocellular carcinoma. The aim of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a5689a9c975423e9aaed0f2f6f84f79
http://europepmc.org/articles/PMC6942134
http://europepmc.org/articles/PMC6942134
Autor:
Jae Sung Ko, Cho Rong Lee, Gyeong Hoon Kang, Hyoung Jin Kang, Sung-Gyoo Park, Choong Ho Shin, Solha Hwang, Murim Choi, Hye-Eun Kim, Sun Mi Baek, Jin Soo Moon, Jeong Kee Seo, Sangmoon Lee
Publikováno v:
Journal of Allergy and Clinical Immunology. 137(1):327-330
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0dae0b38672bb8c0d54070ef90805d8
Autor:
Jeong Kee Seo, Hye Ran Yang, Jung Ok Shim, Jae Sung Ko, Jin Soo Moon, Sung Sup Park, Ju Young Chang
Publikováno v:
Journal of Korean Medical Science
Background Mutations in ATP7B cause Wilson disease (WD). However, direct DNA full sequencing cannot detect all mutations in patients with WD. Multiplex ligation-dependent probe amplification (MLPA) analysis is reportedly useful in increasing the diag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41ed3b43065a7f03f9d99c898233ecd4
https://doi.org/10.3346/jkms.2018.33.e177
https://doi.org/10.3346/jkms.2018.33.e177
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 61:285-291
Objective: The aim of the present study was to investigate the genetic polymorphisms of the autophagy-associated genes autophagy-related 16-like 1 (ATG16L1), immunity-related GTPase M (IRGM), Unc-51-like kinase 1 (ULK1), and NOD2 with respect to earl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::085e18089410d8c48688b05fc1bac0ce
https://doi.org/10.1097/mpg.0000000000000796
https://doi.org/10.1097/mpg.0000000000000796
Autor:
Jeong Kee Seo1 jkseo@snu.ac.kr
Publikováno v:
Pediatric Gastroenterology, Hepatology & Nutrition. Dec2012, Vol. 15 Issue 4, p197-209. 13p.
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 57:570-575
OBJECTIVE Several studies have indicated that plasma citrulline levels reflect the extent of mucosal injury of the small intestine. This study was performed to determine whether plasma citrulline levels correlate with the disease activity in pediatri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f190ce7589c85e40409afe791693aa1
https://doi.org/10.1097/mpg.0b013e31829e264e
https://doi.org/10.1097/mpg.0b013e31829e264e
Autor:
Jeong Wan Seo, Jae Sung Ko, Jae Hee Lee, Jung Hwan Choi, Hae Il Cheong, Jeong Kee Seo, Jeana Hong
Publikováno v:
European Journal of Pediatrics. 172:545-550
Congenital chloride diarrhea (CLD, OMIM#214700) is an autosomal recessive disorder caused by mutations in the solute carrier family 26 member 3 (SLC26A3) gene, which encodes an intestinal chloride/bicarbonate exchanger. While more than 50 mutations h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d8b1b5763254c980bb49d60e4d90f19
https://doi.org/10.1007/s00431-012-1905-3
https://doi.org/10.1007/s00431-012-1905-3
Publikováno v:
World journal of gastroenterology. 22(20)
To investigate clinical profiles and mutations of ABCB11 in Koreans with progressive familial intrahepatic cholestasis 2 and review the differences between Koreans and others.Of 47 patients with neonatal cholestasis, five infants had chronic intrahep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a93b5a3546adca6053de75140c43306
https://pubmed.ncbi.nlm.nih.gov/27239116
https://pubmed.ncbi.nlm.nih.gov/27239116