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Potential Benefits and Perils of Incorporating ChatGPT to the Movement Disorders Clinic

Deik A

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Adult-Onset Genetic Leukoencephalopathies With Movement Disorders

Fu MH, Chang YY

Genetic leukoencephalopathies (GLEs) are a group of white matter abnormalities with heterogeneous radiological and phenotypic features. Although these conditions have mostly been described in children, adult-onset cases are increasingly recognized...
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Myorhythmia and Other Movement Disorders in Two Patients With Coronavirus Disease 2019 Encephalopathy

Hoe RHM, Yang F, Shuit SK, Yong GKW, Puah SH, Ting JSJ, Sadasiv MS, Umapathi T

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Diagnosis Versus Classification of Essential Tremor: A Research Perspective

Erro R, Picillo M, Pellecchia MT, Barone P

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Preservation of Dopamine Transporters in a Patient With Micrographia Due to Cerebral Infarction: A Case Report

Arakaki Y, Yoshimoto T, Ishiyama H, Tanaka T, Hattori Y, Ihara M

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The Clinical Characterization of Blocking Tics in Patients With Tourette Syndrome

Baizabal-Carvallo JF, Jankovic J

Objective Tourette syndrome (TS) is a neurodevelopmental disorder characterized by the presence of motor and phonic tics. Blocking phenomena, characterized by arrests in motor activity causing interruptions in movements or...
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A Brief History of NBIA Gene Discovery

Hayflick SJ

Neurodegenerative disorders associated with high basal ganglia iron are known by the overarching term of ‘NBIA’ disorders or ‘neurodegeneration with brain iron accumulation’. Discovery of their individual genetic bases was...
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Periodic Jaw-Opening Myoclonus in Subacute Sclerosing Panencephalitis

Garg D, Kumar A, Sharma S

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Absence of Alpha-Synuclein Pathology in the Stomach of a Patient With Prodromal Dementia With Lewy Bodies

Shin C, Kim SI, Park SH, Shin JH, Lee CY, Kim HJ, Lee HJ, Kong SH, Suh YS, Yang HK, Jeon B

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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

Hwangbo J, Lee MJ, Kim SJ, Lee J

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Investigation of the Long-Term Effects of Amantadine Use in Parkinson’s Disease

Park S, Shin JH, Jeon SH, Lee CY, Kim HJ, Jeon B

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Wall-Eyed Bilateral Internuclear Ophthalmoplegia Syndrome in a Patient With Progressive Supranuclear Palsy: A Case Report and Literature Review

Kim A, Jung YJ, Yoo D, Shin C, Jeong SH

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Gastrointestinal Dysfunction in Parkinson’s Disease: Neuro-Gastroenterology Perspectives on a Multifaceted Problem

Tan AH, Chuah KH, Beh YY, Schee JP, Mahadeva S, Lim SY

Patients with Parkinson’s disease (PD) face a multitude of gastrointestinal (GI) symptoms, including nausea, bloating, reduced bowel movements, and difficulties with defecation. These symptoms are common and may accumulate during...
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Sex and Gender Influence Urinary Symptoms and Management in Multiple System Atrophy

Bailey ES, Hooshmand SJ, Badihian N, Sandroni P, Benarroch EE, Bower JH, Low PA, Singer W, Coon EA

Objective Multiple system atrophy (MSA) is characterized by urinary dysfunction, yet the influence of sex and gender on urinary symptoms and treatment is unclear. We sought to characterize sex...
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Reliability and Validity of the Embouchure Dystonia Severity Rating Scale

Mantel T, Lee A, Furuya S, Morise M, Altenmüller E, Haslinger B

Objective Embouchure dystonia (ED) is a task-specific movement disorder that leads to loss of fine motor control of the embouchure and tongue muscles in wind musicians. In contrast to...
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Novel Compound Heterozygous Mutations in the SYNE1 Gene in a Taiwanese Family: A Case Report and Literature Review

Kuo CY, Yu PS, Chao CY, Wang CC, Fan WL, Wu YR

Mutations in the synaptic nuclear envelope protein 1 (SYNE1) gene are associated with substantial clinical heterogeneity. Here, we report the first case of SYNE1 ataxia in Taiwan due to two...
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Safinamide as an Adjunct to Levodopa in Asian and Caucasian Patients With Parkinson’s Disease and Motor Fluctuations: A Post Hoc Analysis of the SETTLE Study

Bhidayasiri R, Ishida T, Kamei T, Husni RE, Suzuki I, Wu SL, Cho JW

Objective Safinamide is a selective, reversible monoamine oxidase B inhibitor with demonstrated efficacy and tolerability in placebo-controlled studies and is clinically useful for patients with motor fluctuations. This study evaluated...
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Clinical Characteristics, Genetic Features, and Long-Term Outcome of Wilson’s Disease in a Taiwanese Population: An 11-Year Follow-Up Study

Fan SP, Kuo YC, Lee NC, Chien YH, Hwu WL, Huang YH, Lin HI, Tseng TC, Su TH, Tzeng SR, Hsu CT, Chen HL, Lin CH, Ni YH

ObjectiveaaWilson’s disease (WD) is a rare genetic disorder of copper metabolism, and longitudinal follow-up studies are limited. We performed a retrospective analysis to determine the clinical characteristics and long-term outcomes...
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