Zobrazeno 1 - 10
of 107
pro vyhledávání: '"Kyung-Wook Kang"'
Autor:
Kang-Ho Choi, Ja-Hae Kim, Jae-Myung Kim, Kyung-Wook Kang, Joon-Tae Kim, Seong-Min Choi, Man-Seok Park, Ki-Hyun Cho
Publikováno v:
Journal of Stroke, Vol 23, Iss 2, Pp 285-288 (2021)
Externí odkaz:
https://doaj.org/article/ce2f51dee4824535aaf7256fd49f7d0b
Autor:
Kang-Ho Choi, Ja-Hae Kim, Changho Lee, Jae-Myung Kim, Kyung-Wook Kang, Joon-Tae Kim, Seong-Min Choi, Man-Seok Park, Ki-Hyun Cho
Publikováno v:
Journal of Stroke, Vol 23, Iss 2, Pp 273-276 (2021)
Externí odkaz:
https://doaj.org/article/de52021d210141e9866adbb6eb4c4f13
Autor:
Seung-Hyun Min, Joon-Tae Kim, Kyung-Wook Kang, Min-Ji Choi, Hana Yoon, Yuki Shinohara, Michael H Lev, Jeffrey L Saver, Ki-Hyun Cho
Publikováno v:
PLoS ONE, Vol 15, Iss 3, p e0229836 (2020)
BACKGROUND AND PURPOSE:We hypothesized that admission insular infarcts could be associated with early neurological deterioration (END) in acute minor stroke with large vessel occlusion. METHODS:Using acute and follow-up diffusion-weighted imaging (DW
Externí odkaz:
https://doaj.org/article/5384fa42b14444f586db4b3817c861d5
Autor:
You-Ri Kang, Tai-Seung Nam, Jae-Myung Kim, Kyung Wook Kang, Seong-Min Choi, Seung-Han Lee, Byeong C. Kim, Myeong-Kyu Kim
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
BackgroundTo analyze the clinical phenotype of hereditary spastic paraplegia (HSP) caused by SPG11 mutations (SPG11-HSP).MethodsAmong the 17 patients with sporadic HSP who performed whole exome sequencing analysis, six were diagnosed with SPG11-HSP.
Externí odkaz:
https://doaj.org/article/3c2ce49d42d544549867204349e6adea
Autor:
You-Ri Kang, Tai-Seung Nam, Jae-Myung Kim, Kyung Wook Kang, Seung-Han Lee, Seong-Min Choi, Myeong-Kyu Kim
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Alexander disease (AxD) is a rare autosomal dominant astrogliopathy caused by mutations in the gene encoding for glial fibrillary acidic protein. AxD is divided into two clinical subtypes: type I and type II AxD. Type II AxD usually manifests bulbosp
Externí odkaz:
https://doaj.org/article/a60cd334984f456a8fde75844e7bc8d3
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
BackgroundThe 2019 coronavirus disease (COVID-19) pandemic has been associated with a significant increase in sleep disorders. This study aimed to determine the prevalence of restless leg syndrome (RLS) and the effect of COVID-19 on RLS during the pa
Externí odkaz:
https://doaj.org/article/ae9d711fb8b74bdcb7225716d6b5242f
Publikováno v:
Medicina, Vol 59, Iss 9, p 1573 (2023)
Background: Aside from primary pseudotumor cerebri syndrome (PTCS) with an unknown etiology (i.e., idiopathic intracranial hypertension), which typically occurs in association with obesity, several conditions including cerebral venous abnormalities,
Externí odkaz:
https://doaj.org/article/7c65985683a24961b4ca264d8a364a62
Autor:
You-Ri Kang, Kun-Hee Kim, Tai-Seung Nam, Kyung-Hwa Lee, Kyung Wook Kang, Seung-Jin Lee, Seok-Yong Choi, Gopalakrishnan Chandrasekaran, Myeong-Kyu Kim
Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
Anti-melanoma differentiation-associated gene 5 (anti-MDA5) antibody is a myositis-specific marker detected in clinically amyopathic dermatomyositis (DM). DM with anti-MDA5 antibody can be accompanied by rapidly progressive interstitial lung disease
Externí odkaz:
https://doaj.org/article/59c8febc44264228b3fed2f4b1120d30
Publikováno v:
Epilia: Epilepsy and Community. 4:68-72
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8da1a50bb5211e316a1e207413e8a8b2
https://doi.org/10.35615/epilia.2022.00368
https://doi.org/10.35615/epilia.2022.00368
Autor:
Kyung Wook Kang, Wonkuk Kim, Yong Won Cho, Sang Kun Lee, Ki-Young Jung, Wonchul Shin, Dong Wook Kim, Won-Joo Kim, Hyang Woon Lee, Woojun Kim, Keuntae Kim, So-Hyun Lee, Seok-Yong Choi, Myeong-Kyu Kim
Publikováno v:
PeerJ, Vol 7, p e8278 (2019)
Background Knowledge of the genetic etiology of epilepsy can provide essential prognostic information and influence decisions regarding treatment and management, leading us into the era of precision medicine. However, the genetic basis underlying epi
Externí odkaz:
https://doaj.org/article/30eadd62d9f74b40b003291739f7b13e