- Presynaptic Dopaminergic Dysfunction Was Overestimated in Huntington’s Disease Presenting as Young Age-Onset Parkinsonism
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Kim T, Choi BJ, Lyoo CH
- KMID: 2533699
- J Mov Disord.
- 2022 Sep;15(3):293-295.
- doi: 10.14802/jmd.22071
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- Anti-LGI1 Antibody Limbic Encephalitis Presented with Amnestic Mild Cognitive Impairment
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Kim HK, Cho H, Lyoo CH
- KMID: 2153168
- J Korean Neurol Assoc.
- 2016 Feb;34(1):71-73.
- doi: 10.17340/jkna.2016.1.15
No abstract available. -
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- Asymmetric Parkinsonism With Progressive Nigrosomal Change Secondary to Kernohan’s Notch Phenomenon
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Kim HK, Baek MS, Ahn SJ, Lyoo CH
- KMID: 2530229
- J Mov Disord.
- 2022 May;15(2):184-186.
- doi: 10.14802/jmd.21162
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- Novel Ferritin Light Chain Gene Mutation in a Korean Patient with Neuroferritinopathy
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Yoon SH, Kim NY, Kim YJ, Lyoo CH
- KMID: 2438684
- J Mov Disord.
- 2019 Jan;12(1):63-65.
- doi: 10.14802/jmd.18062
No abstract available. -
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- A Patient with Neuroferritinopathy Presenting with Juvenile-Onset Voice Tremor
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Park CW, Kim NY, Kim YJ, Song SK, Lyoo CH
- KMID: 2501672
- J Mov Disord.
- 2020 Jan;13(1):66-68.
- doi: 10.14802/jmd.19038
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- A Patient with Recurrent Dyskinesia and Hyperpyrexia Syndrome
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Baek MS, Lee HW, Lyoo CH
- KMID: 2395014
- J Mov Disord.
- 2017 Sep;10(3):154-157.
- doi: 10.14802/jmd.17022
Dyskinesia hyperpyrexia syndrome is a rare medical emergency in Parkinson's disease. It is characterized by continuous dyskinesia associated with hyperthermia, rhabdomyolysis, and alteration of the mental state. We present the... -
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- Optical Coherence Tomography Findings Facilitate the Diagnosis of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
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Cho H, Lyoo CH, Park SE, Seo Y, Han SH, Han J
- KMID: 2518980
- Korean J Ophthalmol.
- 2021 Aug;35(4):330-331.
- doi: 10.3341/kjo.2021.0032
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- Cortical Hypometabolism in Opsoclonus-Myoclonus Syndrome
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Lee SH, La YG, Lyoo CH, Lee MS
- KMID: 2184645
- J Korean Neurol Assoc.
- 2015 May;33(2):103-105.
- doi: 10.17340/jkna.2015.2.6
Opsoclonus-myoclonus syndrome (OMS) is characterized by opsoclonus and arrhythmic myoclonic jerks predominantly involving the trunk, limbs, and head. We present two patients with OMS after respiratory tract infection who exhibited... -
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- A Spinocerebellar Ataxia Type 6 Patient Caused by De Novo Expansion of Normal Range CAG Repeats
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Jung DE, Lyoo CH
- KMID: 2554819
- J Korean Neurol Assoc.
- 2024 May;42(2):150-152.
- doi: 10.17340/jkna.2023.0105
Spinocerebellar ataxia type 6 (SCA6) is classified as a CAG repeat disorder, where the number of expanded CAG repeats often undergoes meiotic instability, when transmitted from one generation to the... -
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- Three Patients With Classic and Atypical Neurodegeneration With Brain Iron Accumulation
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Lee SY, Lyoo CH, Seo KD, Lee MS
- KMID: 2185069
- J Korean Neurol Assoc.
- 2008 Aug;26(3):243-246.
Neurodegeneration with brain iron accumulation (NBIA) is a disorder characterized by various mixtures of extrapyramidal, pyramidal or psychiatric abnormalities associated with iron accumulation in the basal ganglia. The mutations in... -
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- Inadequate Efficacy of Deep Brain Stimulation in a Patient with Parkinson's disease due to Partial Breakage of Electrode Lead
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Lyoo CH, Chang JW, Lee MS
- KMID: 1852265
- J Korean Neurol Assoc.
- 2005 Dec;23(6):820-822.
A patient with Parkinson's disease developed fluctuation in the deep brain stimulation (DBS) effect, an unpleasant left facial paresthesia and the left limb dystonia. Impedance of the right DBS was... -
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- Apolipoprotein E Polymorphism in Schizophrenic Patients
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Choi YS, Lim CK, Lyoo CH
- KMID: 2340567
- J Korean Neuropsychiatr Assoc.
- 2001 May;40(3):503-509.
OBJECTIVES: To explore the role of apolipoprotein E in schizophrenia, we investigated apoli-poprotein E polymorphism in groups of patients with schizophrenia and normal controls. We also examined the relationship of... -
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- A Patient with Genetically Confirmed Myoclonus-Dystonia Responded to Anticholinergic Treatment and Improved Spontaneously
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Lee JH, Lyoo CH, Lee MS
- KMID: 2179010
- J Clin Neurol.
- 2011 Dec;7(4):231-232.
- doi: 10.3988/jcn.2011.7.4.231
BACKGROUND: The various medical treatments applied to myoclonus-dystonia patients with a mutation of the epsilon-sarcoglycan gene (SGCE) have not been beneficial in most cases. Most patients experience progressive deterioration or... -
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- Huntington's Disease Confirmed by Genetic and Pathological Study
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Lyoo CH, Lee MS, Kim YJ, Suk SH, Yang KH, Song KS
- KMID: 2342560
- J Korean Neurol Assoc.
- 1996 Sep;14(3):725-737.
Huntington's disease is an autosomal dominantly inherited neurodegenerative disease, which is characterized by choreic movement and progressive dementia. A definite diagnosis of Huntington's disease cannot be made by clinical informations... -
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- Subthalamic Deep Brain Stimulation for Parkinson's Disease
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Lyoo CH, Chang JW, Lee MS
- KMID: 1572446
- J Korean Neurol Assoc.
- 2006 Jun;24(3):191-203.
The recent progress in the basic knowledge of basal ganglia pathways and advances in the techniques of the neuroimaging studies enabled subthalamic deep brain stimulation (STN DBS). In Korea, more... -
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- Increased Uptake of AV-1451 in a Subacute Infarction Lesion
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Cho SH, Cho H, Park S, Ryu YH, Choi JY, Lyoo CH, Na DL, Seo SW, Kim HJ
- KMID: 2410912
- Yonsei Med J.
- 2018 Jun;59(4):563-565.
- doi: 10.3349/ymj.2018.59.4.563
¹â¸F-AV-1451 is a tau PET ligand that has high affinity for paired helical filament tau. However, various off-target bindings unrelated to tau have also been reported. Herein, we report a... -
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- A family with machado-joseph disease confirmed by gene analysis
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Lyoo CH, Kim YD, Lee MS
- KMID: 2442970
- J Korean Neurol Assoc.
- 1997 Apr;15(2):403-412.
The Machado Joseph disease(MJD) is a progressive neurodegenerative disease with an autosomal dominant inheritance. Patients affected by MJD may present variable combinations of cerebellar ataxia, ophthalmoplegia, pyramidal tract signs, extrapyramidal... -
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- Parkin Gene Mutation in Korean Patients with Young Age Onset Sporadic Parkinson's Disease
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Lee KO, Lyoo CH, Lee MS
- KMID: 1957673
- J Korean Neurol Assoc.
- 2006 Feb;24(1):26-30.
BACKGROUND: Abnormalities of the parkin gene is the most frequently found genetic abnormality in patients with sporadic young age onset of Parkinson's disease (PD). We investigated the frequency of abnormalities... -
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- A Familial Case of Myoclonus-Dystonia
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Oh SH, Kim HS, Lyoo CH, Lee JG, Lee MS
- KMID: 2343018
- J Korean Neurol Assoc.
- 2002 Sep;20(5):509-514.
BACKGROUND: Myoclonus-dystonia is a rare familial disease characterized by autosomal dominant inheritance, nonor slowly progressive axial myoclonus combined with dystonic posture, normal electroencephalography (EEG) finding, and dramatic response to alcohol... -
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- Point Mutations at alpha-Synuclein Gene are not Found in Korean Familial Parkinson's Disease
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Lyoo CH, Kim HS, Kim YD, Kim JH, Lee MS
- KMID: 1905133
- J Korean Neurol Assoc.
- 1999 Jul;17(4):534-540.
BACKGROUND: Recent developments of molecular biological techniques have enabled the identification of genetic abnormalities responsible for the development of familial Parkinson's disease (PD). The alpha-synuclein, a major component of Lewy... -
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