Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sook Kun Song"'
Autor:
Hyun Sook Kim, Chul Hyoung Lyoo, Phil Hyu Lee, Sang Jin Kim, Mee Young Park, Hyeo-Il Ma, Jae Hyeok Lee, Sook Kun Song, Jong Sam Baik, Jin Ho Kim, Myung Sik Lee
Publikováno v:
Journal of Movement Disorders, Vol 8, Iss 1, Pp 14-20 (2015)
Objective Huntington’s disease (HD) is a rare neurological disorder, and its current status in Korea is not well investigated. This study aims to determine the prevalence and incidence of HD and to investigate the clinical features of HD patients i
Externí odkaz:
https://doaj.org/article/87330b40af7740048826d0c7ed27e4e0
Autor:
Jun Kyu Mun, Jinyoung Youn, Jin Whan Cho, Eung-Seok Oh, Ji Sun Kim, Suyeon Park, Wooyoung Jang, Jin Se Park, Seong-Beom Koh, Jae Hyeok Lee, Hee Kyung Park, Han-Joon Kim, Beom S Jeon, Hae-Won Shin, Sun-Ah Choi, Sang Jin Kim, Seong-Min Choi, Ji-Yun Park, Ji Young Kim, Sun Ju Chung, Chong Sik Lee, Tae-Beom Ahn, Won Chan Kim, Hyun Sook Kim, Sang Myung Cheon, Jae Woo Kim, Hee-Tae Kim, Jee-Young Lee, Eun-Joo Kim, Jong-Min Kim, Kwang Soo Lee, Joong-Seok Kim, Min-Jeong Kim, Jong Sam Baik, Ki-Jong Park, Hee Jin Kim, Mee Young Park, Ji Hoon Kang, Sook Kun Song, Yong Duk Kim, Ji Young Yun, Ho-Won Lee, In-Uk Song, Young H Sohn, Phil Hyu Lee, Jeong-Ho Park, Hyung Geun Oh, Kun Woo Park, Do-Young Kwon
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0162254 (2016)
Despite the clinical impact of non-motor symptoms (NMS) in Parkinson's disease (PD), the characteristic NMS in relation to the motor subtypes of PD is not well elucidated. In this study, we enrolled drug-naïve PD patients and compared NMS between PD
Externí odkaz:
https://doaj.org/article/22e83ff02f354480b891e9d6fa76c87e
Autor:
Phil Hyu Lee, Hyeo Il Ma, Jae-Hyeok Lee, Jong Sam Baik, Mee Young Park, Sook Kun Song, Jin Ho Kim, Chul Hyoung Lyoo, Myung Sik Lee, Hyun Kim, Sang Jin Kim
Publikováno v:
Journal of Movement Disorders, Vol 8, Iss 1, Pp 14-20 (2015)
Journal of Movement Disorders
Journal of Movement Disorders
Huntington’s disease (HD) is a well-known neurological disorder of inherited genetic cause, the incurable nature of which has made patients and doctors helpless. Even after the discovery of the CAG repeat expansion of the IT-15 gene in 1993, no sat
Autor:
Jinyoung Youn, Ho-Won Lee, Ji Young Kim, Min Jeong Kim, Ji Young Yun, Seong Min Choi, Ji-Hoon Kang, Young H. Sohn, Mee Young Park, Han Joon Kim, Eun-Joo Kim, Kun Woo Park, Jinwhan Cho, Jong Min Kim, In Uk Song, Jeong-Ho Park, Tae-Beom Ahn, Seong Beom Koh, Yong Duk Kim, Ki-Jong Park, Kwang-Soo Lee, Jae-Hyeok Lee, Hae-Won Shin, Beom S. Jeon, Ji Yun Park, Joong-Seok Kim, Sun Ju Chung, Ji Sun Kim, Jae Woo Kim, Do Young Kwon, Chong Sik Lee, Hyung Geun Oh, Hyunsook Kim, Hee Jin Kim, Won Chan Kim, Sang Jin Kim, Hee Tae Kim, Jong Sam Baik, Sang Myung Cheon, Hee Kyung Park, Sook Kun Song, Phil Hyu Lee, Sun Ah Choi, Jee Young Lee
Publikováno v:
Journal of Clinical Neurology (Seoul, Korea)
Background and Purpose Nonmotor symptoms (NMS) in Parkinson's disease (PD) have multisystem origins with heterogeneous manifestations that develop throughout the course of PD. NMS are increasingly recognized as having a significant impact on the heal
Publikováno v:
Neurology. 75(22)
Objective: To explore the neuroanatomic basis of amnestic mild cognitive impairment (aMCI) in patients with Parkinson disease (PD; aMCI-PD + ) and without PD (aMCI-PD − ). Methods: A total of 119 patients with aMCI (aMCI-PD − , n = 78, and aMCI-P