- A Case of MRI-Negative Encephalomyelitis in a Patient With Long-Term Stable Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease
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Hwangbo J, Oh Si
- KMID: 2543824
- J Clin Neurol.
- 2023 Jul;19(4):422-424.
- doi: 10.3988/jcn.2022.0433
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- The Frequency of Korean Patients With Parkinson’s Disease Carrying GBA Mutations in a Subgroup With Age at Onset ≤ 55 Years Old
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Hwangbo J, Lee MJ, Kim SJ, Lee J
- KMID: 2542426
- J Mov Disord.
- 2023 May;16(2):207-209.
- doi: 10.14802/jmd.22191
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- A New Positive Sign of Functional Weakness in Conversion Disorder: Polysomnography with Extended Surface Electromyography
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Hwangbo J, Kang MR, Ji KH
- KMID: 2511104
- J Sleep Med.
- 2020 Dec;17(2):188-191.
- doi: 10.13078/jsm.200025
Patients often present with combinations of psychological disorders that manifest with neurological symptoms and/or signs that are not attributable to identifiable structural or functional etiology associated with the nervous system.... -
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- Prosopometamorphopsia and Visual Field Defect Improved by Valproic acid in a CADASIL Patient
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Hwangbo J, Cho JW, Jung SH, Shin JH, Jung NY
- KMID: 2464140
- J Korean Neurol Assoc.
- 2019 Nov;37(4):368-371.
- doi: 10.17340/jkna.2019.4.5
Persistent aura without infarction is defined as an aura persisting for 1 week or more without evidence of infarction on neuroimaging. It is difficult to differentiate persistent visual aura without... -
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- Gerstmann-Sträussler-Scheinker Disease (Pro102Leu) Presenting as Rapidly Progressive Dementia
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Jung SH, Chae SH, Hwangbo J, Kim HS, Lee YJ, Kim YS, Jung NY
- KMID: 2464144
- J Korean Neurol Assoc.
- 2019 Nov;37(4):384-387.
- doi: 10.17340/jkna.2019.4.9
Genetic prion diseases account for about 10-15% of all cases of human prion disease and are caused by mutations in the prion protein gene. Gerstmann-Sträussler-Scheinker (GSS) disease is a rare... -
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