Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Hwa-Kyoung Chung"'
Autor:
Won-Chul Cho, Jae Seok Song, Byong-Gon Park, Hwa-Kyoung Chung, Hye Yeon Park, Daeho Kwon, Woon-Seob Shin, Seung Hee Choi
Publikováno v:
Molecular & Cellular Toxicology. 15:57-63
Ethylenethiourea (ETU) is one of the main metabolite of ethylenebisdithiocarbamate fungicides and potential exposure is highest for workers involved in rubber and fungicide production. Exposure of ETU induces endocrine disruption, teratogenesis, carc
Autor:
Byong-Gon Park, Daeho Kwon, Yoon-Sun Park, Jae Seok Song, Woon-Seob Shin, Hwa-Kyoung Chung, Seong-Chun Kwon
Publikováno v:
Molecular & Cellular Toxicology. 14:105-112
In the present study, we evaluated the mancozeb-induced toxicity on the liver, thyroid, and testis via histological and functional hormone assay in male rats. Mancozeb was orally administered at 800 mg/kg body weight/day for 4 weeks. Upon the chronic
Autor:
Jeong Hyun Yoo, Hyang Woon Lee, Yun Seo Choi, A-reum Jung, Hwa-Kyoung Chung, Hyeon Jin Kim, Chang-hyun Park
Publikováno v:
The Journal of Neuropsychiatry and Clinical Neurosciences. 29:343-350
Brain functional integration can be disrupted in patients with temporal lobe epilepsy (TLE), but the clinical relevance of this disruption is not completely understood. The authors hypothesized that disrupted functional integration over brain regions
Autor:
Jung Ho Pae, Weonjeong Lim, Hee Yeon Choi, Hwa Kyoung Chung, Seung Sin Lee, Hyang Woon Lee, Jin Woo Kim, Sun Jong Kim
Publikováno v:
The Ewha Medical Journal. 36:79
수면은 휴식을 넘어서 신체와 정신의 건강을 위하여 필요한 과 정으로, 좋은 수면을 유지하는 것은 삶의 질을 높이고 각종 신체, 정신질환을 예방하는 데 중요한 요소이다[1]. 수면의학은 야
Autor:
Hwa Kyoung Chung
Publikováno v:
Neurology. 78:P06.144-P06.144
Objective: The aim of this study is to analysis clinical characteristics of GBS patients and to compare between EGRIS in the acute stage and their clinical outcomes. Background Respiratory difficulty is one of fatal complications in patients with GBS
Autor:
Hwa Kyoung Chung
Publikováno v:
Neurology. 78:P05.145-P05.145
Objective: We report two different types of intermediate AR CMT patients with GDAP1 mutations: a His256Arg homozygous mutation, and two heterozygous Pro111His and Val219Gly mutations. Background Various phenotypes have been reported in Charcot-Marie-
Autor:
Hae Soon Kim, Sung-Hee Kim, Jae Won Hyun, Hyang Woon Lee, Hwa Kyoung Chung, Sung Jin Kim, Ye Ji Choi
Publikováno v:
Journal of Epilepsy Research
Chromosome 22q11.2 deletion syndrome is the most common interstitial deletion syndrome. Major clinical manifestation includes hypocalcemia secondary to hypoparathyroidim. At least 10% of the patients with this syndrome had hypocalcemic seizures which