Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Hyewon Woo"'
Publikováno v:
Annals of Child Neurology, Vol 31, Iss 4, Pp 271-275 (2023)
Purpose We aimed to evaluate the utility of facial analysis technology for genetic diagnoses in a typical pediatric genetic clinic. Methods A retrospective review identified children (aged
Externí odkaz:
https://doaj.org/article/90d8cf7a89b647e88ee130fe32c9dc16
Publikováno v:
Children, Vol 11, Iss 5, p 553 (2024)
Pediatric multiple sclerosis (MS) and neuromyelitis optica (NMO) are rare acquired demyelinating syndrome with limited epidemiological data available, particularly in non-Western setting. This study aimed to demonstrate the epidemiology of pediatric
Externí odkaz:
https://doaj.org/article/2273303165844207a8b1e7fb0e59a5ee
Publikováno v:
Annals of Child Neurology, Vol 31, Iss 3, Pp 219-221 (2023)
Externí odkaz:
https://doaj.org/article/603da5835efd4900b763ff4d6a793cda
Autor:
Soo Yeon Kim, Seungbok Lee, Hyewon Woo, Jiyeon Han, Young Jun Ko, Youngkyu Shim, Soojin Park, Se Song Jang, Byung Chan Lim, Jung Min Ko, Ki Joong Kim, Anna Cho, Hunmin Kim, Hee Hwang, Ji Eun Choi, Man Jin Kim, Jangsup Moon, Moon-Woo Seong, Sung Sup Park, Sun Ah Choi, Ji Eun Lee, Young Se Kwon, Young Bae Sohn, Jon Soo Kim, Won Seop Kim, Yun Jeong Lee, Soonhak Kwon, Young Ok Kim, Hoon Kook, Yong Gon Cho, Chong Kun Cheon, Ki-Soo Kang, Mi-Ryoung Song, Young-Joon Kim, Hyuk-Jin Cha, Hee-Jung Choi, Yun Kee, Sung-Gyoo Park, Seung Tae Baek, Murim Choi, Dong-Sung Ryu, Jong-Hee Chae
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-11 (2022)
Abstract Background Phase I of the Korean Undiagnosed Diseases Program (KUDP), performed for 3 years, has been completed. The Phase I program aimed to solve the problem of undiagnosed patients throughout the country and develop infrastructure, includ
Externí odkaz:
https://doaj.org/article/da31df2b66d24f748e7b60795882af11
Autor:
Hyewon Woo, Seungbok Lee, Ji Yeon Han, Woo Joong Kim, Man Jin Kim, Moon-Woo Seong, Soo Yeon Kim, Anna Cho, Byung Chan Lim, Ki Joong Kim, Jong-Hee Chae
Publikováno v:
Annals of Child Neurology, Vol 30, Iss 3, Pp 127-133 (2022)
Purpose X-linked myotubular myopathy (XLMTM) is a rare condition of centronuclear myopathy caused by myotubularin 1 (MTM1) mutations. Patients with XLMTM show different neurodevelopmental outcomes after the neonatal period depending on age and acquir
Externí odkaz:
https://doaj.org/article/d711970b3a5c4f0f9d2b83b88b2b3566
Autor:
Ji Yeon Han, Seungbok Lee, Hyewon Woo, Soo Yeon Kim, Hunmin Kim, Byung Chan Lim, Hee Hwang, Jieun Choi, Ki Joong Kim, Jong-Hee Chae
Publikováno v:
Annals of Child Neurology, Vol 29, Iss 4, Pp 149-158 (2021)
Purpose The purpose of this study was to expand our understanding of phenotypic and genetic variation in Allan-Herndon-Dudley syndrome (AHDS), which is a rare X-linked mental retardation syndrome characterized by hypotonia, generalized spasticity, an
Externí odkaz:
https://doaj.org/article/e9974141d72343a589a1fa9a051a5f6e
Autor:
Hyewon Woo, Seungbok Lee, Ji Yeon Han, Woo Joong Kim, Man Jin Kim, Moon-Woo Seong, Soo Yeon Kim, Anna Cho, Byung Chan Lim, Ki Joong Kim, Jong-Hee Chae
Publikováno v:
Annals of Child Neurology, Vol 30, Iss 4, Pp 220-220 (2022)
Externí odkaz:
https://doaj.org/article/2371a6cee8474f3d93f814f1883ff622
Autor:
Seungwoo Yoo, Matthew Stremlau, Alejandro Pinto, Hyewon Woo, Olivia Curtis, Henriette van Praag
Publikováno v:
Cells, Vol 10, Iss 7, p 1778 (2021)
Hyperlipidemia and hypertension are modifiable risk factors for cognitive decline. About 25% of adults over age 65 use both antihypertensives (AHTs) and statins to treat these conditions. Recent research in humans suggests that their combined use may
Externí odkaz:
https://doaj.org/article/febc2964b73e4dac95d0df7bdfc8eea6
Publikováno v:
Neurology Asia. 2023, Vol. 28 Issue 4, p1063-1067. 5p.
Publikováno v:
Pediatric Neurology. 139:35-42
Our study aimed to characterize seizure incidence and seizure outcome of pediatric autoimmune encephalitis (AE) focusing on subgroup analysis based on antibody (Ab).Among 110 pediatric patients with AE, we compared seizure characteristics and outcome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dadaeb3c55f59e7e5e27dc64ff8482cc
https://doi.org/10.1016/j.pediatrneurol.2022.11.008
https://doi.org/10.1016/j.pediatrneurol.2022.11.008