Journal of Movement Disorders

Papers
(The TQCC of Journal of Movement Disorders is 3. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-05-01 to 2025-05-01.)
ArticleCitations
Sensitivity of Detecting Alpha-Synuclein Accumulation in the Gastrointestinal Tract and Tissue Volume Examined37
Retinal Thinning as a Marker of Disease Severity in Progressive Supranuclear Palsy24
Efficacy and Safety of Zolpidem for Musician’s Dystonia24
Effect of Chelation Therapy on a Korean Patient With Brain Manganese Deposition Resulting From a Compound Heterozygous Mutation in the SLC39A14 Gene23
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Masquerading as Charcot-Marie-Tooth Disease: A Case Study and Literature Review of Korean Patients23
Investigation of the Long-Term Effects of Amantadine Use in Parkinson’s Disease19
The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene19
Knowledge, Attitudes and Perceptions of Genetic Testing Among Patients With Movement Disorders, Their Caregivers and Health Care Professionals18
Evaluating the Validity and Reliability of the Korean Version of the Scales for Outcomes in Parkinson’s Disease–Cognition18
DHDDS Mutation: A Rare Cause of Refractory Epilepsy and Hyperkinetic Movement Disorder16
Pain Characteristics of Parkinson’s Disease Using Validated Arabic Versions of the King’s Parkinson’s Disease Pain Scale and Questionnaire: A Multicenter Egyptian Study16
Comparing Montreal Cognitive Assessment Performance in Parkinson’s Disease Patients: Age- and Education-Adjusted Cutoffs vs. Machine Learning15
Muscle Dystonia Manifesting as Unilateral Rectus Abdominis Hypertrophy and Abdominal Pain in Parkinson’s Disease: A Case Report15
TNR Gene Mutation in Familial Parkinson’s Disease: Possible Implications for Essential Tremor14
Dystonic Opisthotonus in Kufor-Rakeb Syndrome: Expanding the Phenotypic and Genotypic Spectrum14
Association Between Gait and Dysautonomia in Patients With De Novo Parkinson’s Disease: Forward Gait Versus Backward Gait14
Syringomyelia Manifesting With Pseudodystonia: A Case Report13
Joubert Syndrome Presenting With Levodopa-Responsive Parkinsonism12
Potential Psychosis Induced by a Sustained High Plasma Levodopa Concentration Due to Continuous Subcutaneous Foslevodopa/Foscarbidopa Infusion in a Patient With Parkinson’s Disease: A Case Report11
The Application of Deep Brain Stimulation in the Syndrome of Irreversible Lithium-Effectuated Neurotoxicity11
Validity and Reliability of the Korean-Translated Version of the International Cooperative Ataxia Rating Scale in Cerebellar Ataxia11
Jaw Opening Myoclonus in Subacute Sclerosing Panencephalitis: A New Phenotypic Observation10
Movement Disorders Resulting From Bilateral Basal Ganglia Lesions in End-Stage Kidney Disease: A Systematic Review10
A Novel Variant of GCH1 in Dopa-Responsive Dystonia With Oculogyric Crises and Intrafamilial Phenotypic Heterogeneity10
Historical and More Common Nongenetic Movement Disorders From Asia10
Association Between Exposure to Particulate Matter and the Incidence of Parkinson’s Disease: A Nationwide Cohort Study in Taiwan10
High Levels of Mutant Huntingtin Protein in Tear Fluid From Huntington’s Disease Gene Expansion Carriers10
Adult-Onset Genetic Leukoencephalopathies With Movement Disorders9
Does Restless Legs Syndrome Have a Different Pathomechanism in Premotor and Motor Parkinson’s Disease?9
Cervical proprioception in Parkinson's disease and its correlation with manual dexterity function8
Content Analysis of Korean Videos Regarding Restless Legs Syndrome on YouTube8
Reliability and Validity of the Embouchure Dystonia Severity Rating Scale7
Absence of Alpha-Synuclein Aggregation in Patients With Parkinson’s Disease Complicated by Sigmoid Volvulus7
Effect of Positional Changes on Cerebral Perfusion in Parkinson’s Disease Patients With Orthostatic Hypotension7
“Face of the Giant Panda” Sign and Bilateral Thalamic Hyperintensity in Isoniazid-Induced Ataxia6
The Clinical Characterization of Blocking Tics in Patients With Tourette Syndrome6
Comment on “A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome”6
The First East Asian Patient With Parkinson’s Disease Caused by the A53E SNCA Mutation With Early Progression to Dementia6
Fecal Calprotectin in Parkinson’s Disease and Multiple System Atrophy6
Rapid-Onset Dystonia and Parkinsonism in a Patient With Gaucher Disease6
Semiautomated Algorithm for the Diagnosis of Multiple System Atrophy With Predominant Parkinsonism5
Shoulder Dysfunction in Parkinson's Disease: Implications of Motor Subtypes, Disease Severity, and Spinopelvic Alignment5
Clinical and Structural Characteristics of NEU1 Variants Causing Sialidosis Type 15
Ataxia and Myoclonus with a Cherry-Red Spot Unfurling an Unusual Phenotypic Presentation of Sialidosis Type 15
Sex and Gender Influence Urinary Symptoms and Management in Multiple System Atrophy5
Copper Deficiency Myeloneuropathy in a Patient With Wilson’s Disease5
Long-Term Outcomes of Deep Brain Stimulation in Pantothenate Kinase-Associated Neurodegeneration-Related Dystonia5
Apomorphine Monotherapy for Parkinson’s Disease: A Neglected Option?5
Challenges in Parkinson’s Disease Care—In Light of the COVID-19 Pandemic5
Acute Extrapyramidal Side Effects Following Domperidone Intake in a 48-Year-Old Female Patient: The First Genetic Alteration and Drug Interaction Characterized5
Evidence of Inflammation in Parkinson’s Disease and Its Contribution to Synucleinopathy5
Brittle Response to Levodopa as a Marker of Parkinson’s Disease Phenotype Characterized by Heavy Motor and Non Motor Burden4
A Novel Pathogenic PSEN1 Variant in a Patient With Dystonia-Parkinsonism Without Dementia4
Encephalopathy and Complex Hyperkinesia in a Patient with Severe Acute Respiratory Syndrome Coronavirus-2 Infection4
Non-Motor Fluctuations in Parkinson’s Disease: Underdiagnosed Yet Important4
From Evidence to the Dish: A Viewpoint of Implementing a Thai-Style Mediterranean Diet for Parkinson’s Disease4
Accuracy of Machine Learning Using the Montreal Cognitive Assessment for the Diagnosis of Cognitive Impairment in Parkinson’s Disease4
The Goal Attainment Scale Refines Patient-Centered Expectations in Botulinum Toxin Treatment of Cervical Dystonia4
Deep Brain Stimulation in Advanced Parkinson’s Disease: An Uncommon Case of Allergic Encephalitis4
Tremulous Dystonia Due to GNAL Haploinsufficiency Caused by 18p Deletion Syndrome4
Extraction of the pull force from inertial sensors during the pull test for Parkinson’s disease: A reliability study4
Adjustability of Gait Speed in Clinics and Free-Living Environments for People With Parkinson’s Disease4
A Practical Guide for Diagnostic Investigations and Special Considerations in Patients With Huntington’s Disease in Korea3
Movement Disorders Associated With Radiotherapy and Surgical Procedures3
Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese Ancestry3
Potential Benefits and Perils of Incorporating ChatGPT to the Movement Disorders Clinic3
Dystonia Responsive to Dopamine: POLG Mutations Should Be Considered If Sensory Neuropathy Is Present3
Myoclonic Epilepsy of Unverricht and Lundborg in a Filipino Woman3
Chorea as a Presentation of SARS-CoV-2 Encephalitis: A Clinical Case Report3
Ocular Vestibular-Evoked Myogenic Potential Assists in the Differentiation of Multiple System Atrophy From Parkinson’s Disease3
Novel Compound Heterozygous Mutations in the SYNE1 Gene in a Taiwanese Family: A Case Report and Literature Review3
Deep Brain Stimulation for Cockayne Syndrome-Associated Movement Disorder3
Oculogyric Crisis as the First Presentation of Biotin-Thiamine-Responsive Basal Ganglia Disease: A Case Report3
Changes in Cerebral Gray and White Matter in Patients with Pantothenate Kinase-Associated Neurodegeneration: A Long-Term Magnetic Resonance Imaging Follow-Up Study3
Wall-Eyed Bilateral Internuclear Ophthalmoplegia Syndrome in a Patient With Progressive Supranuclear Palsy: A Case Report and Literature Review3
A Case of AOA2 With Compound Heterozygous SETX Mutations3
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