Zobrazeno 1 - 10 of 15 pro vyhledávání: '"Sang Kyoon Hong"'
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Akademický článek
A Validation Study of a Smartphone-Based Finger Tapping Application for Quantitative Assessment of Bradykinesia in Parkinson's Disease.
Autor: Chae Young Lee, Seong Jun Kang, Sang-Kyoon Hong, Hyeo-Il Ma, Unjoo Lee, Yun Joong Kim
Publikováno v: PLoS ONE, Vol 11, Iss 7, p e0158852 (2016)
Most studies of smartphone-based assessments of motor symptoms in Parkinson's disease (PD) focused on gait, tremor or speech. Studies evaluating bradykinesia using wearable sensors are limited by a small cohort size and study design. We developed an
Externí odkaz: https://doaj.org/article/6257d00ecd9b4b1797114a6edbf53dc2
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2
Meta-Analysis of Differentially Expressed Genes in the Substantia Nigra in Parkinson’s Disease Supports Phenotype-Specific Transcriptome Changes
Autor: Sang-Kyoon Hong, Jeehee Yoon, Young Eun Kim, Duong My Phung, Jinwoo Lee, Yun Joong Kim
Publikováno v: Frontiers in Neuroscience
Frontiers in Neuroscience, Vol 14 (2020)
BackgroundStudies regarding differentially expressed genes (DEGs) in Parkinson’s disease (PD) have focused on common upstream regulators or dysregulated pathways or ontologies; however, the relationships between DEGs and disease-related or cell typ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::086eb405dc628844499d73c44845fc64
http://europepmc.org/articles/PMC7775392
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3
The burden of rare damaging variants in hereditary atypical parkinsonism genes is increased in patients with Parkinson's disease
Autor: Yoon Shin Cho, Sang-Kyoon Hong, Jinwoo Lee, Nan Young Kim, Yun Joong Kim, Jeehee Yoon
Publikováno v: Neurobiology of aging. 100
Increased burdens of rare coding variants in genes related to lysosomal storage disease or mitochondrial pathways were reported to be associated with idiopathic Parkinson's disease. Under a hypothesis that the burden of damaging rare coding variants
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2733f2ccb42467abf79f679650c2753
https://pubmed.ncbi.nlm.nih.gov/33423827
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4
Dysregulation of the causative genes for hereditary parkinsonism in the midbrain in Parkinson's disease
Autor: Yun Joong Kim, Jae-Min Oh, Young Eun Kim, Unjoo Lee, Jeehee Yoon, Sang-Kyoon Hong, Jeong Hoon Hong, Yeo Jin Kim, Junbeom Jeon, Hyeo-Il Ma, Jaemoon Shin, Nan Young Kim, Suk Yun Kang
Publikováno v: Movement Disorders. 32:1211-1220
Background and Objectives Many hereditary movement disorders with complex phenotypes without a locus symbol prefix for familial PD present as parkinsonism; however, the dysregulation of genes associated with these phenotypes in the SNpc of PD patient
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::49feaefd46a569a45d52f4fc57225281
https://doi.org/10.1002/mds.27019
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5
Familiar Hyperekplexia, a Potential Cause of Cautious Gait: A New Korean Case and a Systematic Review of Phenotypes
Autor: Nan Young Kim, Young H. Sohn, Yoonju Lee, Sang-Kyoon Hong, Phil Hyu Lee, Su Jin Chung, Seong Ho Jeong
Publikováno v: Journal of Movement Disorders, Vol 10, Iss 1, Pp 53-58 (2017)
Journal of Movement Disorders
Familial hyperekplexia, also called startle disease, is a rare neurological disorder characterized by excessive startle responses to noise or touch. It can be associated with serious injury from frequent falls, apnea spells, and aspiration pneumonia.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd64b08117c785e5a7c09450e4101f74
https://doi.org/10.14802/jmd.16044
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6
Tau Accumulation in Primary Motor Cortex of Variant Alzheimer’s Disease with Spastic Paraparesis
Autor: Sang Kyoon Hong, Hanna Cho, Jae Yong Choi, Yun Joong Kim, Young Hoon Ryu, Chul Hyoung Lyoo, Mi Song Hwang, Myung Sik Lee
Publikováno v: Journal of Alzheimer's Disease. 51:671-675
We studied topographic distribution of tau and amyloid-β in a patient with variant Alzheimer's disease with spastic paraparesis (VarAD) by comparing AD patients. The proband developed progressive memory impairment, dysarthria, and spastic paraparesi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3027f29725a45db0eb5370bbf8606974
https://doi.org/10.3233/jad-151052
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8
Neuroimaging studies and whole exome sequencing of PLA2G6-associated neurodegeneration in a family with intrafamilial phenotypic heterogeneity
Autor: Nan Young Kim, Myung Sik Lee, Yun Joong Kim, Sang-Kyoon Hong, Chul Hyoung Lyoo
Publikováno v: Parkinsonism & Related Disorders. 21:402-406
Background PLA2G6 -associated neurodegeneration (PLAN) encompasses infantile- or atypical neuroaxonal dystrophy, and adult-onset dystonia-parkinsonism. Examination of the intrafamilial phenotypic variability of PLAN by neuroimaging data and backgroun
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a21624d037d5e0f7e9379d47e0e792a8
https://doi.org/10.1016/j.parkreldis.2015.01.010
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10
A Validation Study of a Smartphone-Based Finger Tapping Application for Quantitative Assessment of Bradykinesia in Parkinson's Disease
Autor: Sang-Kyoon Hong, Yun Joong Kim, Hyeo-Il Ma, Unjoo Lee, Seong Jun Kang, Chae Young Lee
Publikováno v: PLoS ONE
PLoS ONE, Vol 11, Iss 7, p e0158852 (2016)
PLOS ONE(11): 7
Background Most studies of smartphone-based assessments of motor symptoms in Parkinson's disease (PD) focused on gait, tremor or speech. Studies evaluating bradykinesia using wearable sensors are limited by a small cohort size and study design. We de
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afd41de0ece77c3efbcc6a9e25848f3b
https://pubmed.ncbi.nlm.nih.gov/27467066
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