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 2022-05-01 to 2026-05-01.)
ArticleCitations
Effect of Chelation Therapy on a Korean Patient With Brain Manganese Deposition Resulting From a Compound Heterozygous Mutation in the SLC39A14 Gene37
Efficacy and Safety of Zolpidem for Musician’s Dystonia37
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Masquerading as Charcot-Marie-Tooth Disease: A Case Study and Literature Review of Korean Patients29
Sensitivity of Detecting Alpha-Synuclein Accumulation in the Gastrointestinal Tract and Tissue Volume Examined29
Retinal Thinning as a Marker of Disease Severity in Progressive Supranuclear Palsy29
Anti-IgLON5-Related Movement Disorders: A Series of Three Cases from a Tertiary Centre in India23
The Landscape of Parkinson’s Disease Treatment in India: A National Cross-Sectional Survey of Clinical Practitioners19
The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene17
Knowledge, Attitudes and Perceptions of Genetic Testing Among Patients With Movement Disorders, Their Caregivers and Health Care Professionals16
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
Congenital ataxic phenotype of ITPR1 -related disorder due to novel missense variants – A video case series15
Evaluating the Validity and Reliability of the Korean Version of the Scales for Outcomes in Parkinson’s Disease–Cognition14
Investigation of the Long-Term Effects of Amantadine Use in Parkinson’s Disease14
Neuropsychiatric and cognitive safety of subcutaneous foslevodopa/foscarbidopa in advanced Parkinson’s disease: insights from a real-world cohort14
Muscle Dystonia Manifesting as Unilateral Rectus Abdominis Hypertrophy and Abdominal Pain in Parkinson’s Disease: A Case Report13
Association Between Gait and Dysautonomia in Patients With De Novo Parkinson’s Disease: Forward Gait Versus Backward Gait13
Dystonic Opisthotonus in Kufor-Rakeb Syndrome: Expanding the Phenotypic and Genotypic Spectrum12
Joubert Syndrome Presenting With Levodopa-Responsive Parkinsonism11
Comparing Montreal Cognitive Assessment Performance in Parkinson’s Disease Patients: Age- and Education-Adjusted Cutoffs vs. Machine Learning11
DHDDS Mutation: A Rare Cause of Refractory Epilepsy and Hyperkinetic Movement Disorder11
The Application of Deep Brain Stimulation in the Syndrome of Irreversible Lithium-Effectuated Neurotoxicity10
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 Report9
Validity and Reliability of the Korean-Translated Version of the International Cooperative Ataxia Rating Scale in Cerebellar Ataxia9
Syringomyelia Manifesting With Pseudodystonia: A Case Report9
Adult-Onset Genetic Leukoencephalopathies With Movement Disorders8
High Levels of Mutant Huntingtin Protein in Tear Fluid From Huntington’s Disease Gene Expansion Carriers8
Jaw Opening Myoclonus in Subacute Sclerosing Panencephalitis: A New Phenotypic Observation8
Association Between Exposure to Particulate Matter and the Incidence of Parkinson’s Disease: A Nationwide Cohort Study in Taiwan7
Historical and More Common Nongenetic Movement Disorders From Asia7
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, Cro7
Movement Disorders Resulting From Bilateral Basal Ganglia Lesions in End-Stage Kidney Disease: A Systematic Review7
A Novel Variant of GCH1 in Dopa-Responsive Dystonia With Oculogyric Crises and Intrafamilial Phenotypic Heterogeneity7
Early-Onset Spastic Ataxia in a Patient With the Prion (PRNP) p.Val180Ile Variant7
MRI-Guided Focused Ultrasound in Parkinson’s Disease and Essential Tremor: Incisionless but Invasive. A Narrative Review7
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 function6
The First East Asian Patient With Parkinson’s Disease Caused by the A53E SNCA Mutation With Early Progression to Dementia6
Shoulder Dysfunction in Parkinson’s Disease: Implications of Motor Subtypes, Disease Severity, and Spinopelvic Alignment6
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
“Face of the Giant Panda” Sign and Bilateral Thalamic Hyperintensity in Isoniazid-Induced Ataxia6
Copper Deficiency Myeloneuropathy in a Patient With Wilson’s Disease6
Sex and Gender Influence Urinary Symptoms and Management in Multiple System Atrophy6
Apomorphine Monotherapy for Parkinson’s Disease: A Neglected Option?6
Fecal Calprotectin in Parkinson’s Disease and Multiple System Atrophy6
Reliability and Validity of the Embouchure Dystonia Severity Rating Scale6
Rapid-Onset Dystonia and Parkinsonism in a Patient With Gaucher Disease6
Challenges in Parkinson’s Disease Care—In Light of the COVID-19 Pandemic6
Semiautomated Algorithm for the Diagnosis of Multiple System Atrophy With Predominant Parkinsonism6
The Effects 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
‘Subthreshold’ Expansions in Individuals with Otherwise Typical Clinico-Radiological Features of GAA- FGF14 -Related Cerebellar Ataxia (SCA27B)5
From Evidence to the Dish: A Viewpoint of Implementing a Thai-Style Mediterranean Diet for Parkinson’s Disease5
Extraction of the pull force from inertial sensors during the pull test for Parkinson’s disease: A reliability study5
Adult-onset Familial TUBB4A -related Leukodystrophy Caused by c.286G>A (p.Gly96Arg) in a Korean Family: A Case Report5
Acute Extrapyramidal Side Effects Following Domperidone Intake in a 48-Year-Old Female Patient: The First Genetic Alteration and Drug Interaction Characterized5
Accuracy of Machine Learning Using the Montreal Cognitive Assessment for the Diagnosis of Cognitive Impairment in Parkinson’s Disease5
The Goal Attainment Scale Refines Patient-Centered Expectations in Botulinum Toxin Treatment of Cervical Dystonia5
Successful Treatment of a Patient With Tremors and Extensive Brain Lesions Using Posterior Subthalamic Area–Deep Brain Stimulation5
Long-Term Outcomes of Deep Brain Stimulation in Pantothenate Kinase-Associated Neurodegeneration-Related Dystonia5
A Novel Pathogenic PSEN1 Variant in a Patient With Dystonia-Parkinsonism Without Dementia5
Brittle Response to Levodopa as a Marker of Parkinson’s Disease Phenotype Characterized by Heavy Motor and Non Motor Burden5
Deep Brain Stimulation in Advanced Parkinson’s Disease: An Uncommon Case of Allergic Encephalitis5
Adjustability of Gait Speed in Clinics and Free-Living Environments for People With Parkinson’s Disease5
Non-Motor Fluctuations in Parkinson’s Disease: Underdiagnosed Yet Important4
A Practical Guide for Diagnostic Investigations and Special Considerations in Patients With Huntington’s Disease in Korea4
Diagnosing Cerebrotendinous Xanthomatosis in a Middle-Aged Woman With Cervical Dystonia4
Subtyping of Parkinson’s Disease by Longitudinal Trajectories of Levodopa Equivalent Daily Dose4
Novel Compound Heterozygous Mutations in the SYNE1 Gene in a Taiwanese Family: A Case Report and Literature Review4
Tremulous Dystonia Due to GNAL Haploinsufficiency Caused by 18p Deletion Syndrome4
Potential Benefits and Perils of Incorporating ChatGPT to the Movement Disorders Clinic4
Diagnostic Spectrum in an “Atypical” Atypical Parkinsonism Syndrome Cohort: A Single Center Experience4
Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese Ancestry4
Clinical and Pathological Features of CSF1R-Related Disorder Associated with the p.R777Q Pathogenic Variant4
A Case of AOA2 With Compound Heterozygous SETX Mutations4
Myoclonic Epilepsy of Unverricht and Lundborg in a Filipino Woman4
The Role of Handedness and Extrainstrumental Burdens on the Course of Musicians’ Dystonia4
Oculogyric Crisis as the First Presentation of Biotin-Thiamine-Responsive Basal Ganglia Disease: A Case Report4
Atypical Imaging Findings in Corticobasal Syndrome: A Case Report3
Hemimasticatory Spasm Treated With Muscle Afferent Block Therapy and Occlusal Splint3
Revisiting the Triglyceride–Glucose Index in Parkinson’s Disease: Risk Ractor or Disease Marker?3
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 Literature3
Haloperidol in Managing DYT-TOR1A Dystonia: Unveiling a Dramatic Therapeutic Response3
Ocular Vestibular-Evoked Myogenic Potential Assists in the Differentiation of Multiple System Atrophy From Parkinson’s Disease3
NBR and GBA Gene Methylation Levels in the Peripheral Blood of Parkinson’s Disease Patients3
Evidence-Based Review on Symptomatic Management of Huntington’s Disease3
Effective botulinum toxin treatment in different patterns of cervical dystonia: a retrospective SPECT and EMG study3
Movement Disorders Associated With Radiotherapy and Surgical Procedures3
Wall-Eyed Bilateral Internuclear Ophthalmoplegia Syndrome in a Patient With Progressive Supranuclear Palsy: A Case Report and Literature Review3
Clinical and Genetic Features of Huntington’s Disease Patients From Republic of Serbia: 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
Hand Movement-Induced Eyeblink Bursts in a Patient With Parkinson’s Disease2
Two Cases of Genetically Proven SCARB2-Related Progressive Myoclonic Epilepsy Without Renal Failure: A Report From India2
Comparison of the Impact of Various Exercise Modalities on Parkinson’s Disease2
Endurance and Efficiency of Cycling and Manual Wheelchairs in Late-Stage Parkinson’s Disease: A Preliminary Study2
Clinical and Genetic Characterization of Woodhouse-Sakati Syndrome in Iranian Patients: A Case Series2
Tremors in Infantile Tremor Syndrome Mimicking Epilepsia Partialis Continua2
Meige Syndrome as a Craniofacial Type of Dystonia Treatable by Dual Dopaminergic Modulation Using L-DOPA/Chlorpromazine: A Case Report2
The Frequency of Korean Patients With Parkinson’s Disease Carrying GBA Mutations in a Subgroup With Age at Onset ≤ 55 Years Old2
A Case of Post-Malaria Neurological Syndrome Presenting With Cortical Tremor2
Catatonia in Hospitalized Patients With COVID-19: An Important Clinical Finding That Should Not be Missed2
Delayed presentation of Diencephalic-Mesencephalic Junction Dysplasia with Compulsive truncal movements and Blepharospasm: A Case Report from India2
A Cautionary Note on the Indication for Deep Brain Stimulation in Parkinsonism Patients With SLC9A6 Gene Mutations2
A KMT2B Frameshift Variant Causing Focal Dystonia Restricted to the Oromandibular Region After Long-Term Follow-up2
Subjective Cognitive Complaints in Cognitively Normal Patients With Parkinson’s Disease: A Systematic Review2
Effectiveness of Live-Streaming Tele-Exercise Intervention in Patients With Parkinson’s Disease: A Pilot Study2
Myorhythmia and Other Movement Disorders in Two Patients With Coronavirus Disease 2019 Encephalopathy2
GBA1 Variants and Parkinson’s Disease: Paving the Way for Targeted Therapy2
Genetically Proven Ataxia With Vitamin E Deficiency With Predominant Cervicobrachial Dystonic Presentation: A Case Report From India2
Thalamic Deep Brain Stimulation for SPG56-Related Focal Hand Dystonia2
Dopamine Transporter Deficiency Syndrome: A Rare Case of Infantile-Onset Dystonia-Parkinsonism2
Phenotypic Spectrum of Progressive Supranuclear Palsy: Clinical Study and Apolipoprotein E Effect2
A Chinese Child With Dystonia Linked to the EIF2AK2 Missense Variant: A Case Report2
Development of Clinical Milestones in Parkinson’s Disease After Bilateral Subthalamic Deep Brain Stimulation2
Fatigue in Parkinson’s Disease Is Due to Decreased Efficiency of the Frontal Network: Quantitative EEG Analysis2
Safety and Efficacy of Istradefylline in Parkinson’s Disease Patients With and Without Preexisting Dyskinesia: Pooled Analysis of 8 Randomized Controlled Trials2
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
Adult-Onset Alexander Disease With Late-Presenting Vestibulopathy: A Case Report1
Trends in Physiotherapy Interventions and Medical Costs for Parkinson’s Disease in South Korea, 2011–20201
Continuous 24-h Levodopa-Carbidopa Intestinal Gel Infusion After a Levodopa Holiday Suppressed Refractory Dyskinesia Despite Increasing Levodopa Dose1
Gravitational syncope induced by rising elevators in a Parkinson’s disease patient1
The Burden of Rheumatic Chorea in the Modern Era: A Case Series From a Tertiary Health Care Center in South India1
Eye Movement and Gait Variability Analysis in Chinese Patients With Huntington’s Disease1
Caregiver Burden of Patients With Huntington’s Disease in South Korea1
Utility of Clinical Exome Sequencing in Dystonia: A Single-Center Study From India1
Gastrointestinal Dysfunction in Parkinson’s Disease: Neuro-Gastroenterology Perspectives on a Multifaceted Problem1
Absence of Alpha-Synuclein Pathology in the Stomach of a Patient With Prodromal Dementia With Lewy Bodies1
CLCN2-Related Leukoencephalopathy Presenting as Isolated Paroxysmal Non-Kinesigenic Dyskinesia: Clinical, Imaging, and Genetic Correlation1
Labrune’s Syndrome Presenting With Stereotypy-Like Movements and Psychosis: A Case Report and Review1
Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution1
Expanding the Clinical Spectrum of RFC1 Gene Mutations1
Current Status and Future Perspectives on Stem Cell-Based Therapies for Parkinson’s Disease1
Treatable Ataxias: How to Find the Needle in the Haystack?1
Longitudinal Multimodal Functional Imaging: An Essential Tool for Visualizing Pathologic Progression in Parkinson’s Disease1
KMT2B-Related Dystonia in Indian Patients With Literature Review and Emphasis on Asian Cohort1
Comment on “Parainfectious Anti-Glial Fibrillary Acidic Protein-Associated Meningoencephalitis”1
Late-Onset Ataxia, Chorea, Cognitive Impairment, and Insomnia: Expanding the Phenotype of IRF2BPL-Related Disease1
Clinical Characteristics, Genetic Features, and Long-Term Outcome of Wilson’s Disease in a Taiwanese Population: An 11-Year Follow-Up Study1
Pseudodystonia and Neuropathic Tremor in a Patient With Monomelic Amyotrophy1
Gait Parameters in Healthy Older Adults in Korea1
Complete Relief of Tardive Truncal Dystonia With a Low Dose of Levodopa/Carbidopa: A Case Report1
Pisa Syndrome in Subacute Sclerosing Panencephalitis: A Case Report and Review of the Literature1
Ultrastructures of α-Synuclein Filaments in Synucleinopathy Brains and Experimental Models1
Variability in Pull Test Performance Within a Tertiary Movement Disorders Center1
Video-Oculography for Enhancing the Diagnostic Accuracy of Early Oculomotor Dysfunction in Progressive Supranuclear Palsy1
Suprahyoid Tremor as an Early Feature of Multiple System Atrophy-Parkinsonism: A Case Report1
Basal Ganglia Syndrome in a Male With an XK Gene Variant but Without XK Disease (McLeod Syndrome)1
Neurological Perspectives Should Be Integrated Into the Management of Tardive Dyskinesia—Expert Opinions and Proposed Educational Initiatives in Asia1
Potential Link Between Cognition and Motor Reserve in Patients With Parkinson’s Disease1
Presynaptic Dopaminergic Dysfunction Was Overestimated in Huntington’s Disease Presenting as Young Age-Onset Parkinsonism1
Fighting Against the Clock: Circadian Disruption and Parkinson’s Disease1
Task-Specific Drinking Tremor1
A Case of Task-Specific Tremor of the Hand While Driving1
Spatiotemporal Gait Parameters in Adults With Premanifest and Manifest Huntington’s Disease: A Systematic Review1
Olfactory and Gustatory Function in Early-Stage Parkinson’s Disease: Implications for Cognitive Association1
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