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1.
Journal of Clinical Neurology ; : 633-645, 2020.
Article | WPRIM | ID: wpr-833666

ABSTRACT

Background@#and Purpose: The Movement Disorder Society-Sponsored Revision of the Unified Parkinson’s Disease Rating Scale (MDS-UPDRS) is widely used for estimating the symptoms of Parkinson’s disease. Translation and validation of the MDS-UPDRS is necessary for non-English speaking countries and regions. The aim of this study was to validate the Korean version of the MDS-UPDRS. @*Methods@#Altogether, 362 patients in 19 centers were recruited for this study. We translated the MDS-UPDRS to Korean using the translation-back translation method and cognitive pretesting. We performed both confirmatory and exploratory factor analyses to validate the scale.We calculated the comparative fit index (CFI) for confirmatory factor analysis, and used unweighted least squares for exploratory factor analysis. @*Results@#The CFI was higher than 0.90 for all parts of the scale. Exploratory factor analysis also showed that the Korean MDS-UPDRS has the same number of factors in each part as the English version. @*Conclusions@#The Korean MDS-UPDRS has the same overall structure as the English MDSUPDRS. Our translated scale can be designated as the official Korean MDS-UPDRS.

2.
Journal of the Korean Neurological Association ; : 363-366, 2016.
Article in Korean | WPRIM | ID: wpr-179061

ABSTRACT

A 70-year-old woman underwent cardiopulmonary bypass surgery for aorta dissection. After 10 days she developed a vertical gaze palsy, and 2 months later she presented with dysarthria, bradykinesia, postural instability, blepharospasm, and truncal tilt to the left. Brain imaging indicated old lacunes in the bilateral thalamus. Her symptoms remained unchanged during a 4-year follow-up, which seems to be incompatible with progressive supranuclear palsy (PSP). However, the clinical features of this case were suggestive of PSP-like syndrome after cardiopulmonary bypass surgery.


Subject(s)
Aged , Female , Humans , Aorta , Blepharospasm , Cardiopulmonary Bypass , Dysarthria , Follow-Up Studies , Hypokinesia , Neuroimaging , Paralysis , Parkinsonian Disorders , Supranuclear Palsy, Progressive , Thalamus
3.
Journal of Clinical Neurology ; : 146-148, 2009.
Article in English | WPRIM | ID: wpr-180082

ABSTRACT

BACKGROUND: Multiple sclerosis (MS) is a demyelinating disease of the central nervous system. Secondary amyloidosis can occur as a complication of chronic systemic inflammatory and infectious diseases. Until now there has been no report of secondary amyloidosis associated with MS. We report herein a case of renal biopsy-proven secondary amyloidosis in a patient with MS. CASE REPORT: A 41-year-old woman with MS was hospitalized due to aggravated quadriparesis and edema in both lower extremities. Laboratory findings showed nephrotic-range proteinuria and hypoalbuminemia. A percutaneous renal biopsy procedure was performed, the results of which revealed secondary amyloid-A-type amyloidosis associated with MS. CONCLUSIONS: This is the first report of secondary amyloidosis associated with MS.


Subject(s)
Adult , Female , Humans , Amyloidosis , Biopsy , Central Nervous System , Communicable Diseases , Demyelinating Diseases , Edema , Hypoalbuminemia , Lower Extremity , Multiple Sclerosis , Nephrotic Syndrome , Proteinuria , Quadriplegia
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