Journal of Movement Disorders

Papers
(The median citation count of Journal of Movement Disorders is 1. 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 2021-09-01 to 2025-09-01.)
ArticleCitations
Sensitivity of Detecting Alpha-Synuclein Accumulation in the Gastrointestinal Tract and Tissue Volume Examined30
Efficacy and Safety of Zolpidem for Musician’s Dystonia28
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Masquerading as Charcot-Marie-Tooth Disease: A Case Study and Literature Review of Korean Patients26
Retinal Thinning as a Marker of Disease Severity in Progressive Supranuclear Palsy25
Anti-IgLON5 Related Movement Disorders: A Series Of Three Cases From a Tertiary Centre in India24
Effect of Chelation Therapy on a Korean Patient With Brain Manganese Deposition Resulting From a Compound Heterozygous Mutation in the SLC39A14 Gene20
Evaluating the Validity and Reliability of the Korean Version of the Scales for Outcomes in Parkinson’s Disease–Cognition19
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
Pain Characteristics of Parkinson’s Disease Using Validated Arabic Versions of the King’s Parkinson’s Disease Pain Scale and Questionnaire: A Multicenter Egyptian Study15
Muscle Dystonia Manifesting as Unilateral Rectus Abdominis Hypertrophy and Abdominal Pain in Parkinson’s Disease: A Case Report14
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
Comparing Montreal Cognitive Assessment Performance in Parkinson’s Disease Patients: Age- and Education-Adjusted Cutoffs vs. Machine Learning12
Joubert Syndrome Presenting With Levodopa-Responsive Parkinsonism12
Syringomyelia Manifesting With Pseudodystonia: A Case Report12
DHDDS Mutation: A Rare Cause of Refractory Epilepsy and Hyperkinetic Movement Disorder12
High Levels of Mutant Huntingtin Protein in Tear Fluid From Huntington’s Disease Gene Expansion Carriers11
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
Historical and More Common Nongenetic Movement Disorders From Asia10
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 Report10
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 Heterogeneity9
Association Between Exposure to Particulate Matter and the Incidence of Parkinson’s Disease: A Nationwide Cohort Study in Taiwan9
Does Restless Legs Syndrome Have a Different Pathomechanism in Premotor and Motor Parkinson’s Disease?9
MRI-Guided Focused Ultrasound (MRgFUS) in Parkinson's Disease and Essential Tremor: Incisionless but Invasive! - A Narrative Review8
Adult-Onset Genetic Leukoencephalopathies With Movement Disorders8
Jaw Opening Myoclonus in Subacute Sclerosing Panencephalitis: A New Phenotypic Observation7
Absence of Alpha-Synuclein Aggregation in Patients With Parkinson’s Disease Complicated by Sigmoid Volvulus7
Cervical proprioception in Parkinson's disease and its correlation with manual dexterity function7
Rapid-Onset Dystonia and Parkinsonism in a Patient With Gaucher Disease7
Reliability and Validity of the Embouchure Dystonia Severity Rating Scale7
The First East Asian Patient With Parkinson’s Disease Caused by the A53E SNCA Mutation With Early Progression to Dementia6
Efficacy of Levodopa/Benserazide Dispersible Tablets on “Delayed ON ” to the First Morning Dose in Patients With Parkinson’s Disease With Motor Fluctuations: A Multicenter, Randomized, Open-Label, Cro6
“Face of the Giant Panda” Sign and Bilateral Thalamic Hyperintensity in Isoniazid-Induced Ataxia6
Comment on “A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome”6
Early-onset spastic ataxia in a patient with Prion (PRNP) p.Val180Ile variant6
The Clinical Characterization of Blocking Tics in Patients With Tourette Syndrome6
Effect of Positional Changes on Cerebral Perfusion in Parkinson’s Disease Patients With Orthostatic Hypotension6
Fecal Calprotectin in Parkinson’s Disease and Multiple System Atrophy6
Shoulder Dysfunction in Parkinson’s Disease: Implications of Motor Subtypes, Disease Severity, and Spinopelvic Alignment5
Challenges in Parkinson’s Disease Care—In Light of the COVID-19 Pandemic5
Long-Term Outcomes of Deep Brain Stimulation in Pantothenate Kinase-Associated Neurodegeneration-Related Dystonia5
Copper Deficiency Myeloneuropathy in a Patient With Wilson’s Disease5
Sex and Gender Influence Urinary Symptoms and Management in Multiple System Atrophy5
Ataxia and Myoclonus with a Cherry-Red Spot Unfurling an Unusual Phenotypic Presentation of Sialidosis Type 15
Apomorphine Monotherapy for Parkinson’s Disease: A Neglected Option?5
Semiautomated Algorithm for the Diagnosis of Multiple System Atrophy With Predominant Parkinsonism5
The effect of Biofeedback therapy on Anxiety and Depression in Parkinson's disease: a Pilot Study5
Clinical and Structural Characteristics of NEU1 Variants Causing Sialidosis Type 15
Extraction of the pull force from inertial sensors during the pull test for Parkinson’s disease: A reliability study4
A Novel Pathogenic PSEN1 Variant in a Patient With Dystonia-Parkinsonism Without Dementia4
Accuracy of Machine Learning Using the Montreal Cognitive Assessment for the Diagnosis of Cognitive Impairment in Parkinson’s Disease4
Deep Brain Stimulation in Advanced Parkinson’s Disease: An Uncommon Case of Allergic Encephalitis4
Adjustability of Gait Speed in Clinics and Free-Living Environments for People With Parkinson’s Disease4
From Evidence to the Dish: A Viewpoint of Implementing a Thai-Style Mediterranean Diet for Parkinson’s Disease4
Brittle Response to Levodopa as a Marker of Parkinson’s Disease Phenotype Characterized by Heavy Motor and Non Motor Burden4
Tremulous Dystonia Due to GNAL Haploinsufficiency Caused by 18p Deletion Syndrome4
The Goal Attainment Scale Refines Patient-Centered Expectations in Botulinum Toxin Treatment of Cervical Dystonia4
Deep Brain Stimulation for Cockayne Syndrome-Associated Movement Disorder4
Evidence of Inflammation in Parkinson’s Disease and Its Contribution to Synucleinopathy4
Acute Extrapyramidal Side Effects Following Domperidone Intake in a 48-Year-Old Female Patient: The First Genetic Alteration and Drug Interaction Characterized4
Successful Treatment with Posterior Subthalamic Area-Deep Brain Stimulation in a patient with tremor and extensive brain lesion4
Non-Motor Fluctuations in Parkinson’s Disease: Underdiagnosed Yet Important4
Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese Ancestry3
Oculogyric Crisis as the First Presentation of Biotin-Thiamine-Responsive Basal Ganglia Disease: A Case Report3
A Practical Guide for Diagnostic Investigations and Special Considerations in Patients With Huntington’s Disease in Korea3
Ocular Vestibular-Evoked Myogenic Potential Assists in the Differentiation of Multiple System Atrophy From Parkinson’s Disease3
The Role of handedness and extrainstrumental burdens on the course of musicians’ dystonia3
Atypical imaging findings in corticobasal syndrome: a case report3
Diagnosing Cerebrotendinous Xanthomatosis in a Middle-Aged Woman With Cervical Dystonia3
Chorea as a Presentation of SARS-CoV-2 Encephalitis: A Clinical Case Report3
A Case of AOA2 With Compound Heterozygous SETX Mutations3
Myoclonic Epilepsy of Unverricht and Lundborg in a Filipino Woman3
Revisiting the triglyceride-glucose index in Parkinson’s disease: Risk factor or disease marker?3
Diagnostic Spectrum in an “Atypical” Atypical Parkinsonism Syndrome Cohort: A Single Center Experience3
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 Study3
Wall-Eyed Bilateral Internuclear Ophthalmoplegia Syndrome in a Patient With Progressive Supranuclear Palsy: A Case Report and Literature Review3
Potential Benefits and Perils of Incorporating ChatGPT to the Movement Disorders Clinic3
Novel Compound Heterozygous Mutations in the SYNE1 Gene in a Taiwanese Family: A Case Report and Literature Review3
Movement Disorders Associated With Radiotherapy and Surgical Procedures3
Subtyping of Parkinson’s Disease by Longitudinal Trajectories of Levodopa Equivalent Daily Dose3
Evidence-Based Review on Symptomatic Management of Huntington’s Disease3
Safety and Efficacy of Istradefylline in Parkinson’s Disease Patients With and Without Preexisting Dyskinesia: Pooled Analysis of 8 Randomized Controlled Trials2
Clinico-Genetic Profiles of Seven Patients With PINK1-Related Parkinson’s Disease: A Case Series From a Tertiary Care Centre in India and a Review of the Literature2
Haloperidol in Managing DYT-TOR1A Dystonia: Unveiling a Dramatic Therapeutic Response2
Clinical and Genetic Features of Huntington’s Disease Patients From Republic of Serbia: A Single-Center Experience2
GBA1 Variants and Parkinson’s Disease: Paving the Way for Targeted Therapy2
Two Cases of Genetically Proven SCARB2-Related Progressive Myoclonic Epilepsy Without Renal Failure: A Report From India2
Phonatory Characteristics of Male Patients with Classic Essential Tremor2
Hand Movement-Induced Eyeblink Bursts in a Patient With Parkinson’s Disease2
Focused Vibrotactile Stimulation with Cueing Effect on Freezing of Gait in Parkinson’s Disease: Two Case Reports2
Hemimasticatory Spasm Treated With Muscle Afferent Block Therapy and Occlusal Splint2
The Frequency of Korean Patients With Parkinson’s Disease Carrying GBA Mutations in a Subgroup With Age at Onset ≤ 55 Years Old2
Effectiveness of Live-Streaming Tele-Exercise Intervention in Patients With Parkinson’s Disease: A Pilot Study2
Rotatory ‘head on bed’ alleviating maneuver in Pantothenate Kinase Associated Neurodegeneration2
Meige Syndrome as a Craniofacial Type of Dystonia Treatable by Dual Dopaminergic Modulation Using L-DOPA/Chlorpromazine: A Case Report2
Acquired Movement Disorders Secondary to Giant Tumefactive Perivascular Spaces2
NBR and GBA Gene Methylation Levels in the Peripheral Blood of Parkinson’s Disease Patients2
Myorhythmia and Other Movement Disorders in Two Patients With Coronavirus Disease 2019 Encephalopathy2
A Case of Post-Malaria Neurological Syndrome Presenting With Cortical Tremor2
Fatigue in Parkinson’s Disease Is Due to Decreased Efficiency of the Frontal Network: Quantitative EEG Analysis2
Increased Mortality in Young-Onset Parkinson’s Disease2
Pseudodystonia and Neuropathic Tremor in a Patient With Monomelic Amyotrophy1
Late-Onset Ataxia, Chorea, Cognitive Impairment, and Insomnia: Expanding the Phenotype of IRF2BPL-Related Disease1
A Case of Task-Specific Tremor of the Hand While Driving1
Tremors in Infantile Tremor Syndrome Mimicking Epilepsia Partialis Continua1
Management of Parkinson’s Disease in the COVID-19 Pandemic and Future Perspectives in the Era of Vaccination1
Investigation of Nocturnal Hypokinesia and Health-Related Quality of Life in Parkinsonian Patients with the Korean Version of the Nocturnal Hypokinesia Questionnaire1
Pisa Syndrome in Subacute Sclerosing Panencephalitis: A Case Report and Review of the Literature1
Clinical and Imaging Profile of Patients with Joubert Syndrome1
Dopamine Transporter Deficiency Syndrome: A Rare Case of Infantile-Onset Dystonia-Parkinsonism1
Clinical profile and Genetic Composition of patients with Juvenile Parkinsonism from a single tertiary care center in India1
Subjective Cognitive Complaints in Cognitively Normal Patients With Parkinson’s Disease: A Systematic Review1
Re: Comments on “Chorea as a Presentation of SARS-CoV-2 Encephalitis: A Clinical Case Report”1
Clinical and Genetic Characterization of Woodhouse-Sakati Syndrome in Iranian Patients: A Case Series1
Task-Specific Dystonia in a Professional Billiard Player1
Utility of Clinical Exome Sequencing in Dystonia: A Single-Center Study From India1
The Burden of Rheumatic Chorea in the Modern Era: A Case Series From a Tertiary Health Care Center in South India1
Absence of Alpha-Synuclein Pathology in the Stomach of a Patient With Prodromal Dementia With Lewy Bodies1
Spatiotemporal Gait Parameters in Adults With Premanifest and Manifest Huntington’s Disease: A Systematic Review1
Gait Parameters in Healthy Older Adults in Korea1
Phenotypic Spectrum of Progressive Supranuclear Palsy: Clinical Study and Apolipoprotein E Effect1
Labrune’s Syndrome Presenting With Stereotypy-Like Movements and Psychosis: A Case Report and Review1
A KMT2B Frameshift Variant Causing Focal Dystonia Restricted to the Oromandibular Region After Long-Term Follow-up1
Thalamic Deep Brain Stimulation for SPG56-Related Focal Hand Dystonia1
Dancing Feet Dyskinesia in a Patient with GBA-PD1
A Cautionary Note on the Indication for Deep Brain Stimulation in Parkinsonism Patients With SLC9A6 Gene Mutations1
Variability in Pull Test Performance Within a Tertiary Movement Disorders Center1
Ultrastructures of α-Synuclein Filaments in Synucleinopathy Brains and Experimental Models1
Fighting Against the Clock: Circadian Disruption and Parkinson’s Disease1
Neurological Perspectives Should Be Integrated Into the Management of Tardive Dyskinesia—Expert Opinions and Proposed Educational Initiatives in Asia1
Dopamine Dysregulation Syndrome Presenting as Overuse of Mucuna pruriens Levodopa Supplement1
Validation of the Thai Version of the Movement Disorder Society-Sponsored Revision of the Unified Parkinson's Disease Rating Scale1
Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution1
Complete Relief of Tardive Truncal Dystonia With a Low Dose of Levodopa/Carbidopa: A Case Report1
A Chinese Child With Dystonia Linked to the EIF2AK2 Missense Variant: A Case Report1
Olfactory and Gustatory Function in Early-Stage Parkinson’s Disease: Implications for Cognitive Association1
Genetically Proven Ataxia With Vitamin E Deficiency With Predominant Cervicobrachial Dystonic Presentation: A Case Report From India1
Comparison of the Impact of Various Exercise Modalities on Parkinson’s Disease1
Catatonia in Hospitalized Patients With COVID-19: An Important Clinical Finding That Should Not be Missed1
Development of Clinical Milestones in Parkinson’s Disease After Bilateral Subthalamic Deep Brain Stimulation1
Delayed presentation of Diencephalic-Mesencephalic Junction Dysplasia with Compulsive truncal movements and Blepharospasm: A Case Report from India1
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