Zobrazeno 1 - 10
of 1 131
pro vyhledávání: '"Jung-In Ko"'
Autor:
Min-Jung Kim, Taegyun Kim, Gil Joon Suh, Woon Yong Kwon, Kyung Su Kim, Yoon Sun Jung, Jung-In Ko, So Mi Shin, A Reum Lee
Publikováno v:
Clinical and Experimental Emergency Medicine, Vol 5, Iss 4, Pp 211-218 (2018)
Objective This study aimed to determine whether simultaneous decreases in the serum levels of cell adhesion molecules (intracellular cell adhesion molecule-1 [ICAM-1], vascular cell adhesion molecule-1 [VCAM-1], and E-selectin) and S100 proteins with
Externí odkaz:
https://doaj.org/article/428dc3345a6e42f78ee69012e3629f02
Autor:
Taegyun Kim, Kyung Su Kim, Gil Joon Suh, Woon Yong Kwon, Yoon Sun Jung, Jung-In Ko, So Mi Shin
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0228111 (2020)
BACKGROUND:The aim of this study was to investigate whether 33% duty cycle increases end-tidal carbon dioxide (ETCO2) level, a surrogate measurement for cardiac output during cardiopulmonary resuscitation (CPR), compared with 50% duty cycle. METHODS:
Externí odkaz:
https://doaj.org/article/5f26fe3cf224479883dd71393def56e1
Publikováno v:
Acute and Critical Care, Vol 34, Iss 3, Pp 232-234 (2019)
Externí odkaz:
https://doaj.org/article/072ad717f7a343eab0c40bf30f1df114
Autor:
Man Jin Kim, Jee-Soo Lee, Seung Won Chae, Sung Im Cho, Jangsup Moon, Jung Min Ko, Jong-Hee Chae, Moon-Woo Seong
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Background Ectodermal dysplasia (ED) is a rare genetic disorder that affects structures derived from the ectodermal germ layer. Results In this study, we analyzed the genetic profiles of 27 Korean patients with ED. Whole exome sequencing (WE
Externí odkaz:
https://doaj.org/article/5e5555b0c8b14cfdaa0a6b8cee224017
Autor:
Jun Sung Moon, Shinae Kang, Jong Han Choi, Kyung Ae Lee, Joon Ho Moon, Suk Chon, Dae Jung Kim, Hyun Jin Kim, Ji A Seo, Mee Kyoung Kim, Jeong Hyun Lim, Yoon Ju Song, Ye Seul Yang, Jae Hyeon Kim, You-Bin Lee, Junghyun Noh, Kyu Yeon Hur, Jong Suk Park, Sang Youl Rhee, Hae Jin Kim, Hyun Min Kim, Jung Hae Ko, Nam Hoon Kim, Chong Hwa Kim, Jeeyun Ahn, Tae Jung Oh, Soo-Kyung Kim, Jaehyun Kim, Eugene Han, Sang-Man Jin, Jaehyun Bae, Eonju Jeon, Ji Min Kim, Seon Mee Kang, Jung Hwan Park, Jae-Seung Yun, Bong-Soo Cha, Min Kyong Moon, Byung-Wan Lee
Publikováno v:
Diabetes & Metabolism Journal, Vol 48, Iss 4, Pp 546-708 (2024)
Externí odkaz:
https://doaj.org/article/1ca1a0c775dc4613bbda82213581a6e5
Autor:
Jung-In Ko, Sang Ook Ha, Min Seok Koo, Miyoung Kwon, Jieun Kim, Jin Jeon, So Hee Park, Sangwoo Shim, Youjin Chang, Taejin Park
Publikováno v:
Clinical and Experimental Emergency Medicine, Vol 2, Iss 4, Pp 244-249 (2015)
Objective Airway management in patients with suspected cervical spine injury is classified as a “difficult airway.” The best device for managing difficult airways is not known. Therefore, we conducted an intubation study simulating patients with
Externí odkaz:
https://doaj.org/article/477e1a19a4a24d4d9c18a4ceafd5a741
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 8, Pp n/a-n/a (2024)
ABSTRACT Introduction Holocarboxylase synthetase deficiency (HLCS deficiency, OMIM #253270) is an exceedingly rare metabolic disorder resulting in multiple carboxylase deficiencies owing to impaired biotin cycle. Clinical manifestations include sever
Externí odkaz:
https://doaj.org/article/4959441a6d4c46a5a75fbc5c95d12ccf
Autor:
Seung Min Shin, Ji Young Lee, Heo Nam Hun, Se Woong Choo, Yong Pyo Jeon, Jaewoo Chung, Jung Ho Ko, Hae-Won Koo, Dong Seoung Shin, Man Ryul Lee, Jae Sang Oh
Publikováno v:
Heliyon, Vol 10, Iss 15, Pp e35205- (2024)
Objective: We aimed to examine the effectiveness and safety of a novel torque-controlled catheter for cerebral angiography. Methods: A total of 417 patients who underwent routine transfemoral cerebral angiography were enrolled in a randomized control
Externí odkaz:
https://doaj.org/article/2512fde5205144419401f6a5c71d74dd
Autor:
Seung Hoon Lee, Seung Han Shin, Jung Min Ko, Boram Kim, Hyeon Sae Oh, Man Jin Kim, Seul Gi Park, Ee-Kyung Kim, Han-Suk Kim
Publikováno v:
Neonatal Medicine, Vol 29, Iss 3, Pp 112-116 (2022)
Schaaf-Yang syndrome (SYS) is a rare genomic imprinting disorder caused by truncating mutations in the paternally derived MAGE family member L2 (MAGEL2) allele. It is also responsible for Prader-Willi syndrome, characterized by neonatal hypotonia, de
Externí odkaz:
https://doaj.org/article/de4e4bed93c04833b55a4930bdab3326
Autor:
Jung Min Ko1,2 jmko@snu.ac.kr
Publikováno v:
Clinical & Experimental Pediatrics. Jul2024, Vol. 67 Issue 7, p356-357. 2p.