Chang-Yoon Kim
University of Ulsan
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Featured researches published by Chang-Yoon Kim.
Neurotoxicology | 2003
Joon-Ho Ahn; Cheol-In Yoo; Choong Ryeol Lee; Ji Ho Lee; Hun Lee; Chang-Yoon Kim; Ji Kang Park; Tadashi Sakai; Chungsik Yoon; Yangho Kim
Characteristic high signal intensities confined to the globus pallidus on T1-weighted magnetic resonance image (MRI) can be observed in manganese (Mn)-exposed workers, however, these high signals should be differentiated from those due to other causes such as fat, hemoglobin breakdown products, melanoma, neurofibromatosis, and calcification. A 39-year-old woman was admitted with mutism and involuntary movements which had developed the day before. She had ingested two packs of liquid herbal medicine containing 0.53 mg of Mn daily for 4 months prior to visiting our hospital. Her MRI showed high signals, confined mainly to the globus pallidus on T1-weighted images. Follow-up brain MRI at an interval of 11 months showed no interval change. Brain computed tomography (CT) at the time of the second MRI showed symmetric calcification on both globus pallidus. Blood levels of liver function tests, calcium, phosphorus, and parathyroid hormone were within normal ranges. The increased signals, which were first presumed to be induced by Mn, were concluded to be due to calcification based on the following reasons. First, follow-up brain MRI at an interval of 11 months did not show any interval change. Second, the ingested amount of 1.06 mg Mn daily for 4 months is even less than that added to mineral supplements for adults. Third, Mn-induced high signals in T1-weighted MRI do not show any abnormal findings in brain CT. The present case report suggests that brain CT should be performed to rule out symmetric calcification on basal ganglia in patients showing increased signals in T1-weighted MRI, but who do not have a significant exposure history to Mn. The present report also showed that the amount of 1.06 mg Mn daily ingested for 4 months did not cause the high signal in brain MRI.
Psychiatry Research-neuroimaging | 2010
Byungsu Kim; Hyun-Sook Kim; Yeon Ho Joo; Jiyoung Lim; Chang-Yoon Kim; Kyuyoung Song
The gene encoding D-amino acid oxidase (DAO), which acts as a receptor for the schizophrenia-associated neurotransmitter, N-methyl-D-aspartate (NMDA), is regarded as a potential candidate gene for schizophrenia. However, the potential association of the DAO gene with schizophrenia has been the subject of some debate. Here, we tested three single nucleotide polymorphisms (SNPs) of DAO in a group of Korean schizophrenia patients, and found no significant association in the overall study subjects. Interestingly, however, we found gender-specific differences in allele distributions, with SNP rs2070586 appearing to act as a risk allele in female schizophrenia patients, but as a protective allele in males. Our data support the hypothesis that DAO plays a role in schizophrenia, possibly in a gender-dependent manner.
Schizophrenia Research | 2016
Jungsun Lee; Chang-Yoon Kim; Yeon Ho Joo; Dominick T. Newell; Sylvain Bouix; Martha Elizabeth Shenton; Marek Kubicki
INTRODUCTION Diffusion weighted MRI (dMRI) is a method sensitive to pathological changes affecting tissue microstructure. Most dMRI studies in schizophrenia, however, have focused solely on white matter. There is a possibility, however, that subtle changes in diffusivity exist in gray matter (GM). Accordingly, we investigated diffusivity in GM in patients with recent onset schizophrenia. METHODS We enrolled 45 patients and 21 age and sex-matched healthy controls. All subjects were evaluated using the short form of the Wechsler Adult Intelligence Scale, the Positive and Negative Syndrome Scale (PANSS), and the video based social cognition scale. DMRI and T1W images were acquired on a 3 Tesla magnet, and mean Fractional Anisotropy (FA), Trace (TR) and volume were calculated for each of the 68 cortical GM Regions of Interest parcellated using FreeSurfer. RESULTS There was no significant difference of FA and GM volume between groups after Bonferroni correction. For the dMRI measures, however, patients evinced increased TR in the left bank of the superior temporal sulcus, the right inferior parietal, the right inferior temporal, and the right middle temporal gyri. In addition, higher TR in the right middle temporal gyrus and the right inferior temporal gyrus, respectively, was associated with decreased social function and higher PANSS score in patients with schizophrenia. CONCLUSION This study demonstrates high sensitivity of dMRI to subtle pathology in GM in recent onset schizophrenia, as well as an association between increased diffusivity in temporal GM regions and abnormalities in social cognition and exacerbation of psychiatric symptoms.
Human Psychopharmacology-clinical and Experimental | 2012
Jung Goo Lee; Jong-Il Lee; Yang-Tae Kim; Kim Ch; Chang-Yoon Kim; Jin-Sang Yoon; So-Young Yoo; Young Hoon Kim
The aim of this study was to evaluate the efficacy and safety of quetiapine fumarate extended release (XR) in the treatment of Korean subjects with acute schizophrenia.
Schizophrenia Research | 2017
Jungsun Lee; Chang-Yoon Kim; Yeon Ho Joo; Dominick T. Newell; Sylvain Bouix; Martha Elizabeth Shenton; Marek Kubicki
a Department of Psychiatry, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea b Psychiatry Neuroimaging Laboratory, Department of Psychiatry, Brigham and Womens Hospital, Harvard Medical School, Boston, MA, USA c VA Boston Healthcare System, Brockton Division, Brockton, MA, USA d Department of Radiology, Brigham and Womens Hospital, Harvard Medical School, Boston, MA, USA
Human Genetics | 2005
Seong-Gene Lee; Yeonho Joo; Byungsu Kim; Seockhoon Chung; Hie-Lim Kim; Inchul Lee; Bo-Youl Choi; Chang-Yoon Kim; Kyuyoung Song
The Journal of Clinical Psychiatry | 2007
Hanik K. Yoo; Soon-Ho Choi; Subin Park; Hee-Ryung Wang; Jin-Pyo Hong; Chang-Yoon Kim
Journal of Nervous and Mental Disease | 2003
Oh-Su Han; Hochang B. Lee; Joon-Ho Ahn; Jong-Ik Park; Maeng-Je Cho; Jin-Pyo Hong; Bong-Jin Hahm; Chang-Yoon Kim
Journal of epilepsy research | 2014
Eun Mi Lee; Joong Koo Kang; Jungsu S. Oh; Jae Seung Kim; Yong-Wook Shin; Chang-Yoon Kim
Clinical Neuropharmacology | 2011
Jung-Sun Lee; Joon-Ho Ahn; Jong-Il Lee; Jong-Hoon Kim; InKwa Jung; Chang-Uk Lee; Jun-Young Lee; Sang-Ick Lee; Chang-Yoon Kim