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Alteration of the corpus callosum in patients with Alzheimer's disease: Deep learning-based assessment

PloS one, 2021-12, Vol.16 (12), p.e0259051-e0259051

2021

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Human-to-mouse prion-like propagation of mutant huntingtin protein

Acta neuropathologica, 2016-10, Vol.132 (4), p.577-592

2016

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Drug-induced Parkinsonism: A strong predictor of idiopathic Parkinson's disease

PloS one, 2021-03, Vol.16 (3), p.e0247354-e0247354

2021

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Task-specific tremor with use of scissors

Movement disorders, 2012-06, Vol.27 (7), p.921-922

2012

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Automatic, Qualitative Scoring of the Interlocking Pentagon Drawing Test (PDT) based on U-Net and Mobile Sensor Data

Sensors (Basel, Switzerland), 2020-02, Vol.20 (5), p.1283

2020

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A Validation Study of a Smartphone-Based Finger Tapping Application for Quantitative Assessment of Bradykinesia in Parkinson's Disease

PloS one, 2016-07, Vol.11 (7), p.e0158852-e0158852

2016

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Significant changes in synovial fluid microRNAs after high tibial osteotomy in medial compartmental knee osteoarthritis: Identification of potential prognostic biomarkers

PloS one, 2020-01, Vol.15 (1), p.e0227596-e0227596

2020

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Targeted next-generation sequencing of well-differentiated rectal, gastric, and appendiceal neuroendocrine tumors to identify potential targets

Human pathology, 2019-05, Vol.87, p.83-94

2019

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Striatal Subregion Analysis Associated with REM Sleep Behavior Disorder in Parkinson's Disease

Journal of integrative neuroscience, 2023-01, Vol.22 (1), p.18-18

2023

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Meta-Analysis of Differentially Expressed Genes in the Substantia Nigra in Parkinson's Disease Supports Phenotype-Specific Transcriptome Changes

Frontiers in neuroscience, 2020-12, Vol.14, p.596105-596105

2020

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RelCurator: a text mining-based curation system for extracting gene–phenotype relationships specific to neurodegenerative disorders

Genes & Genomics, 2023, 45(8), , pp.1025-1036

2023

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Evidence of Inflammation in Parkinson’s Disease and Its Contribution to Synucleinopathy

Journal Of Movement Disorders, 2022, 15(1), , pp.1-14

2022

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Synergistic effects of longitudinal amyloid and vascular changes on lobar microbleeds

Neurology, 2016-10, Vol.87 (15), p.1575

2016

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Genetics of Progressive Supranuclear Palsy

Journal of movement disorders, 2015-09, Vol.8 (3), p.122-129

2015

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Potential Link Between Cognition and Motor Reserve in Patients With Parkinson’s Disease

Journal Of Movement Disorders, 2022, 15(3), , pp.249-257

2022

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Accuracy of Machine Learning Using the Montreal Cognitive Assessment for the Diagnosis of Cognitive Impairment in Parkinson’s Disease

Journal Of Movement Disorders, 2022, 15(2), , pp.132-139

2022

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Microglial inhibition alleviates alpha-synuclein propagation and neurodegeneration in Parkinson's disease mouse model

NPJ Parkinson's Disease, 2024-02, Vol.10 (1), p.32-32, Article 32

2024

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PhenGenVar: A User-Friendly Genetic Variant Detection and Visualization Tool for Precision Medicine

Journal of personalized medicine, 2022-06, Vol.12 (6), p.959

2022

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An interpretable multiparametric radiomics model of basal ganglia to predict dementia conversion in Parkinson’s disease

NPJ Parkinson's Disease, 2023-08, Vol.9 (1), p.127-127, Article 127

2023

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Corticobasal syndrome associated with antiphospholipid syndrome without cerebral infarction

Neurology, 2014-02, Vol.82 (8), p.730

2014

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Novel Ferritin Light Chain Gene Mutation in a Korean Patient with Neuroferritinopathy

Journal Of Movement Disorders, 2019, 12(1), , pp.63-65

2019

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A Patient with Neuroferritinopathy Presenting with Juvenile-Onset Voice Tremor

Journal Of Movement Disorders, 2020, 13(1), , pp.66-68

2020

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Expansion of the clinicopathological and mutational spectrum of Perry syndrome

Parkinsonism & related disorders, 2014-04, Vol.20 (4), p.388-393

2014

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Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease

Neurogenetics, 2008-10, Vol.9 (4), p.263-269

2008

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Alteration of the corpus callosum in patients with Alzheimer's disease: Deep learning-based assessment

Human-to-mouse prion-like propagation of mutant huntingtin protein

Drug-induced Parkinsonism: A strong predictor of idiopathic Parkinson's disease

Task-specific tremor with use of scissors

Automatic, Qualitative Scoring of the Interlocking Pentagon Drawing Test (PDT) based on U-Net and Mobile Sensor Data

A Validation Study of a Smartphone-Based Finger Tapping Application for Quantitative Assessment of Bradykinesia in Parkinson's Disease

Significant changes in synovial fluid microRNAs after high tibial osteotomy in medial compartmental knee osteoarthritis: Identification of potential prognostic biomarkers

Targeted next-generation sequencing of well-differentiated rectal, gastric, and appendiceal neuroendocrine tumors to identify potential targets

Striatal Subregion Analysis Associated with REM Sleep Behavior Disorder in Parkinson's Disease

Meta-Analysis of Differentially Expressed Genes in the Substantia Nigra in Parkinson's Disease Supports Phenotype-Specific Transcriptome Changes

RelCurator: a text mining-based curation system for extracting gene–phenotype relationships specific to neurodegenerative disorders

Evidence of Inflammation in Parkinson’s Disease and Its Contribution to Synucleinopathy

Synergistic effects of longitudinal amyloid and vascular changes on lobar microbleeds

Genetics of Progressive Supranuclear Palsy

Potential Link Between Cognition and Motor Reserve in Patients With Parkinson’s Disease

Accuracy of Machine Learning Using the Montreal Cognitive Assessment for the Diagnosis of Cognitive Impairment in Parkinson’s Disease

Microglial inhibition alleviates alpha-synuclein propagation and neurodegeneration in Parkinson's disease mouse model

PhenGenVar: A User-Friendly Genetic Variant Detection and Visualization Tool for Precision Medicine

An interpretable multiparametric radiomics model of basal ganglia to predict dementia conversion in Parkinson’s disease

Corticobasal syndrome associated with antiphospholipid syndrome without cerebral infarction

Validation of the Korean Version of the Scale for Outcomes in Parkinson’s Disease-Autonomic

Novel Ferritin Light Chain Gene Mutation in a Korean Patient with Neuroferritinopathy

A Patient with Neuroferritinopathy Presenting with Juvenile-Onset Voice Tremor

Expansion of the clinicopathological and mutational spectrum of Perry syndrome

Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease

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