Differential Genetic Susceptibility in Diphasic and Peak-Dose Dyskinesias in Parkinson's Disease
SCA in Korea and its regional distribution: A multicenter analysis
Overnight switch from ropinirole to transdermal rotigotine patch in patients with Parkinson disease
No correlation between COMT genotype and entacapone benefits in Parkinson's disease
Wilson's Disease only Presenting with Isolated Unilateral Resting Tremor
Atypical hereditary spastic paraplegia with thin corpus callosum in a Korean patient with a novel SPG11 mutation
A Korean Parkinson's disease family with the LRRK2 p.Tyr1699Cys mutation showing clinical heterogeneity
Diffusion tensor imaging of freezing of gait in patients with white matter changes
A Novel PANK2 Gene Mutation with Sudden-Onset Dystonia
Factors Contributing to Spousal and Offspring Caregiver Burden in Parkinson's Disease
A Parkinson's disease patient with camptocormia caused by an esophageal hiatal hernia
Is cerebral white matter involvement helpful in the diagnosis of dentatorubral-pallidoluysian atrophy
Globus Pallidus Interna Deep Brain Stimulation Improves Chorea and Functional Status in a Patient with Chorea-Acanthocytosis
Validation of the Korean-Version of the Nonmotor Symptoms Scale for Parkinson's Disease
Characteristics of neurological Wilson's disease without Kayser-Fleischer ring
Caregiver Burden in Parkinson Disease With Dementia Compared to Alzheimer Disease in Korea
Decreased Metabolism in the Cerebral Cortex in Early-Stage Huntington's Disease: A Possible Biomarker of Disease Progression
Bedside cognitive assessments and falls risk in Parkinson's disease
Translation and Validation of the Korean Version of the 39-Item Parkinson's Disease Questionnaire
Nonmotor Symptoms in Drug-Induced Parkinsonism and Drug-Naive Parkinson Disease
Waveform analysis of tremor may help to differentiate Parkinson's disease from drug-induced parkinsonism
Restless legs syndrome in Korean patients with drug-naive Parkinson's disease: A nation-wide study
Comparison study of olfactory function and substantia nigra hyperechogenicity in idiopathic REM sleep behavior disorder, Parkinson's disease and normal control
Safety and Effectiveness of Microvascular Decompression for the Treatment of Hemifacial Spasm in the Elderly
Cardiac sympathetic denervation in Parkinson's disease patients with SWEDDs
Thyroid MIBG uptake in Parkinson's disease with diabetes mellitus
OculNon-Ataxic Phenotypes of SCA8 Mimicking Amyotrophic Lateral Sclerosis and Parkinson Disease
ar motor characteristics of different subtypes of spinocerebellar ataxia: Distinguishing features
Short and Long Term Outcome of Bilateral Pallidal Stimulation in Chorea-Acanthocytosis
Topographic distribution of cortical thinning in subtypes of multiple system atrophy
Intravenous amantadine on freezing of gait in Parkinson's disease: a randomized controlled trial
Clinical Manifestations in Paroxysmal Kinesigenic Dyskinesia Patients with Pro line-Rich Transmembrane Protein 2 Gene Mutation
Ataxia-Telangiectasia with Novel Splicing Mutations in the ATM Gene
Safety and efficacy of recombinant human erythropoietin treatment of non-motor symptoms in Parkinson's disease
Effects of repetitive transcranial magnetic stimulation on freezing of gait in patients with Parkinsonism
Topographic pattern of cortical thinning with consideration of motor laterality in Parkinson disease
Alterations of mean diffusivity of pedunculopontine nucleus pathway in Parkinson's disease patients with freezing of gait
Dysport and Botox at a Ratio of 2.5:1 Units in Cervical Dystonia: A Double-Blind, Randomized Study
Outcome of Gamma Knife Thalamotomy in Patients with an Intractable Tremor
Vestibular Performance During High-Acceleration Stimuli Correlates with Clinical Decline in SCA6
Differences in early speech patterns between Parkinson variant of multiple system atrophy and Parkinson's disease
Efficacy of cumulative high-frequency rTMS on freezing of gait in Parkinson's disease
Cognitive Impairment and Its Structural Correlates in the Parkinsonian Subtype of Multiple System Atrophy
Cognitive and Motor Aspects of Parkinson's Disease Associated with Dysphagia
Deep brain stimulation in a dentatorubral-pallidoluyisian atrophy patient with myoclonic dystonia
Cognitive and motor aspects of Parkinson’s disease associated with dysphagia
Deep brain stimulation in a dentatorubral-pallidoluyisian atrophy patient with myoclonic dystonia.
Postural sensory correlates of freezing of gait in Parkinson's disease
Uremic parkinsonism with atypical phenotypes and radiologic features
Atrophy of the Cerebellar Vermis in Essential Tremor: Segmental Volumetric MRI Analysis
Weight Change Is a Characteristic Non-Motor Symptom in Drug-Naive Parkinson's Disease Patients with Non-Tremor Dominant Subtype: A Nation-Wide Observational Study
EFFECT OF CUMULATIVE REPETITIVE TRANS CRANIAL MAGNETIC STIMULATION ON FREEZING OF GAIT IN PATIENTS WITH ATYPICAL PARKINSONISM: A PILOT STUDY
Reply to letter: The association of postural sensory deficit with freezing of gait in Parkinson's disease
Differential Progression of Midbrain Atrophy in Parkinsonism: Longitudinal MRI Study
Effect of cumulative repetitive transcranial magnetic stimulation on freezing of gait in patients with atypical Parkinsonism: A pilot study
Weight Change Is a Characteristic Non-Motor Symptom in Drug-Na?ve Parkinson’s Disease Patients with Non-Tremor Dominant Subtype: A Nation-Wide Observational Study
24-Hour Ambulatory Blood Pressure Monitoring in SWEDDs Patients With Parkinsonism
Atrophy of the cerebellar vermis in essential tremor: Segmental volumetric MRI analysis
Postural sensory correlates of freezing of gait in Parkinson's disease
The composite autonomic symptom scale 31 is a useful screening tool for patients with Parkinsonism
Levodopa dose maintenance or reduction in patients with Parkinson's disease transitioning to levodopa/carbidopa/entacapone
Effect of Dual-Mode and Dual-Site Noninvasive Brain Stimulation on Freezing of Gait in Patients With Parkinson Disease
Psychiatric symptoms in myoclonus-dystonia syndrome are just concomitant features regardless of the SGCE gene mutation
Gender Differences of Nonmotor Symptoms Affecting Quality of Life in Parkinson Disease
Pisa Syndrome in Parkinson's Disease: Pathogenic Roles of Verticality Perception Deficits
Validation of the Korean Version of the Scales for Outcomes in Parkinson's Disease-Sleep
Characteristic Motor and Nonmotor Symptoms Related to Quality of Life in Drug-Naive Patients with Late-Onset Parkinson Disease
Severe Hemifacial Spasm is a Predictor of Severe Indentation and Facial Palsy after Microdecompression Surgery
The Etiologies of Chronic Progressive Cerebellar Ataxia in a Korean Population
Association between White Matter Lesions and Non-Motor Symptoms in Parkinson Disease
Bilateral subthalamic deep brain stimulation is an effective and safe treatment option for the older patients with Parkinson's disease
Inflammatory mediators resulting from transglutaminase 2 expressed in mast cells contribute to the development of Parkinson's disease in a mouse model
Identifying SYNE1 ataxia and extending the mutational spectrum in Korea
Behavioural and trait changes in parkinsonian patients with impulse control disorder after switching from dopamine agonist to levodopa therapy: results of REIN-PD trial
Genetic variants of PARK genes in Korean patients with early-onset Parkinson's disease
Comparison of gait parameters between drug-naive patients diagnosed with multiple system atrophy with predominant parkinsonism and Parkinson's disease
Type 1 Sialidosis Patient With a Novel Deletion Mutation in the NEU1 Gene: Case Report and Literature Review
Prevalence of fragile X-associated tremor/ataxia syndrome: A survey of essential tremor patients with cerebellar signs or extrapyramidal signs
Residual signs of dopa-responsive dystonia with GCH1 mutation following levodopa treatment are uncommon in Korean patients
Midbrain atrophy patients with presymptomatic progressive supranuclear palsy-Richardson's syndrome
Dopa Responsive Parkinsonism in an Early Onset Alzheimer's Disease Patient with a Presenilin 1 Mutation (A434T)
Differential value of brain magnetic resonance imaging in multiple system atrophy cerebellar phenotype and spinocerebellar ataxias