Journal of Movement Disorders

Papers
(The median citation count of Journal of Movement Disorders is 2. 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 2022-06-01 to 2026-06-01.)
ArticleCitations
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Masquerading as Charcot-Marie-Tooth Disease: A Case Study and Literature Review of Korean Patients40
Efficacy and Safety of Zolpidem for Musician’s Dystonia38
Anti-IgLON5-Related Movement Disorders: A Series of Three Cases from a Tertiary Centre in India32
Retinal Thinning as a Marker of Disease Severity in Progressive Supranuclear Palsy30
Sensitivity of Detecting Alpha-Synuclein Accumulation in the Gastrointestinal Tract and Tissue Volume Examined23
Evaluating the Validity and Reliability of the Korean Version of the Scales for Outcomes in Parkinson’s Disease–Cognition18
The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene16
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 Study15
Investigation of the Long-Term Effects of Amantadine Use in Parkinson’s Disease14
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 Spectrum13
DHDDS Mutation: A Rare Cause of Refractory Epilepsy and Hyperkinetic Movement Disorder12
Association Between Gait and Dysautonomia in Patients With De Novo Parkinson’s Disease: Forward Gait Versus Backward Gait11
Comparing Montreal Cognitive Assessment Performance in Parkinson’s Disease Patients: Age- and Education-Adjusted Cutoffs vs. Machine Learning11
Joubert Syndrome Presenting With Levodopa-Responsive Parkinsonism10
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
Jaw Opening Myoclonus in Subacute Sclerosing Panencephalitis: A New Phenotypic Observation8
Adult-Onset Genetic Leukoencephalopathies With Movement Disorders8
High Levels of Mutant Huntingtin Protein in Tear Fluid From Huntington’s Disease Gene Expansion Carriers8
Association Between Exposure to Particulate Matter and the Incidence of Parkinson’s Disease: A Nationwide Cohort Study in Taiwan7
MRI-Guided Focused Ultrasound in Parkinson’s Disease and Essential Tremor: Incisionless but Invasive. A Narrative Review7
Effect of Positional Changes on Cerebral Perfusion in Parkinson’s Disease Patients With Orthostatic Hypotension7
Movement Disorders Resulting From Bilateral Basal Ganglia Lesions in End-Stage Kidney Disease: A Systematic Review7
Historical and More Common Nongenetic Movement Disorders From Asia7
Early-Onset Spastic Ataxia in a Patient With the Prion (PRNP) p.Val180Ile Variant7
A Novel Variant of GCH1 in Dopa-Responsive Dystonia With Oculogyric Crises and Intrafamilial Phenotypic Heterogeneity7
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
Rapid-Onset Dystonia and Parkinsonism in a Patient With Gaucher Disease7
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
Apomorphine Monotherapy for Parkinson’s Disease: A Neglected Option?6
“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
The Effects of Biofeedback Therapy on Anxiety and Depression in Parkinson’s Disease: A Pilot Study6
Reliability and Validity of the Embouchure Dystonia Severity Rating Scale6
Absence of Alpha-Synuclein Aggregation in Patients With Parkinson’s Disease Complicated by Sigmoid Volvulus6
Semiautomated Algorithm for the Diagnosis of Multiple System Atrophy With Predominant Parkinsonism6
Challenges in Parkinson’s Disease Care—In Light of the COVID-19 Pandemic6
From Evidence to the Dish: A Viewpoint of Implementing a Thai-Style Mediterranean Diet for Parkinson’s Disease5
The Clinical Characterization of Blocking Tics in Patients With Tourette Syndrome5
Deep Brain Stimulation in Advanced Parkinson’s Disease: An Uncommon Case of Allergic Encephalitis5
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
Brittle Response to Levodopa as a Marker of Parkinson’s Disease Phenotype Characterized by Heavy Motor and Non Motor Burden5
Extraction of the pull force from inertial sensors during the pull test for Parkinson’s disease: A reliability study5
The Goal Attainment Scale Refines Patient-Centered Expectations in Botulinum Toxin Treatment of Cervical Dystonia5
Clinical and Structural Characteristics of NEU1 Variants Causing Sialidosis Type 15
A Novel Pathogenic PSEN1 Variant in a Patient With Dystonia-Parkinsonism Without Dementia5
Tremulous Dystonia Due to GNAL Haploinsufficiency Caused by 18p Deletion Syndrome5
Potential Benefits and Perils of Incorporating ChatGPT to the Movement Disorders Clinic4
The Role of Handedness and Extrainstrumental Burdens on the Course of Musicians’ Dystonia4
Ocular Vestibular-Evoked Myogenic Potential Assists in the Differentiation of Multiple System Atrophy From Parkinson’s Disease4
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 Korea4
Oculogyric Crisis as the First Presentation of Biotin-Thiamine-Responsive Basal Ganglia Disease: A Case Report4
Subtyping of Parkinson’s Disease by Longitudinal Trajectories of Levodopa Equivalent Daily Dose4
Movement Disorders Associated With Radiotherapy and Surgical Procedures4
Non-Motor Fluctuations in Parkinson’s Disease: Underdiagnosed Yet Important4
Novel Compound Heterozygous Mutations in the SYNE1 Gene in a Taiwanese Family: A Case Report and Literature Review4
Diagnosing Cerebrotendinous Xanthomatosis in a Middle-Aged Woman With Cervical Dystonia4
Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese Ancestry4
Diagnostic Spectrum in an “Atypical” Atypical Parkinsonism Syndrome Cohort: A Single Center Experience4
Myoclonic Epilepsy of Unverricht and Lundborg in a Filipino Woman4
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
Safety and Efficacy of Istradefylline in Parkinson’s Disease Patients With and Without Preexisting Dyskinesia: Pooled Analysis of 8 Randomized Controlled Trials3
Atypical Imaging Findings in Corticobasal Syndrome: A Case Report3
Hemimasticatory Spasm Treated With Muscle Afferent Block Therapy and Occlusal Splint3
Evidence-Based Review on Symptomatic Management of Huntington’s Disease3
A Case of Post-Malaria Neurological Syndrome Presenting With Cortical Tremor3
Myorhythmia and Other Movement Disorders in Two Patients With Coronavirus Disease 2019 Encephalopathy3
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
NBR and GBA Gene Methylation Levels in the Peripheral Blood of Parkinson’s Disease Patients3
Two Cases of Genetically Proven SCARB2-Related Progressive Myoclonic Epilepsy Without Renal Failure: A Report From India3
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
Subjective Cognitive Complaints in Cognitively Normal Patients With Parkinson’s Disease: A Systematic Review2
Dopamine Transporter Deficiency Syndrome: A Rare Case of Infantile-Onset Dystonia-Parkinsonism2
Spatiotemporal Gait Parameters in Adults With Premanifest and Manifest Huntington’s Disease: A Systematic Review2
Genetically Proven Ataxia With Vitamin E Deficiency With Predominant Cervicobrachial Dystonic Presentation: A Case Report From India2
The Frequency of Korean Patients With Parkinson’s Disease Carrying GBA Mutations in a Subgroup With Age at Onset ≤ 55 Years Old2
GBA1 Variants and Parkinson’s Disease: Paving the Way for Targeted Therapy2
Phenotypic Spectrum of Progressive Supranuclear Palsy: Clinical Study and Apolipoprotein E Effect2
Dopamine Dysregulation Syndrome Presenting as Overuse of Mucuna pruriens Levodopa Supplement2
Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution2
Thalamic Deep Brain Stimulation for SPG56-Related Focal Hand Dystonia2
Clinical and Genetic Characterization of Woodhouse-Sakati Syndrome in Iranian Patients: A Case Series2
Meige Syndrome as a Craniofacial Type of Dystonia Treatable by Dual Dopaminergic Modulation Using L-DOPA/Chlorpromazine: A Case Report2
Fatigue in Parkinson’s Disease Is Due to Decreased Efficiency of the Frontal Network: Quantitative EEG Analysis2
A Chinese Child With Dystonia Linked to the EIF2AK2 Missense Variant: A Case Report2
Olfactory and Gustatory Function in Early-Stage Parkinson’s Disease: Implications for Cognitive Association2
Comparison of the Impact of Various Exercise Modalities on Parkinson’s Disease2
A KMT2B Frameshift Variant Causing Focal Dystonia Restricted to the Oromandibular Region After Long-Term Follow-up2
A Cautionary Note on the Indication for Deep Brain Stimulation in Parkinsonism Patients With SLC9A6 Gene Mutations2
Catatonia in Hospitalized Patients With COVID-19: An Important Clinical Finding That Should Not be Missed2
Effectiveness of Live-Streaming Tele-Exercise Intervention in Patients With Parkinson’s Disease: A Pilot Study2
Tremors in Infantile Tremor Syndrome Mimicking Epilepsia Partialis Continua2
Variability in Pull Test Performance Within a Tertiary Movement Disorders Center2
Pisa Syndrome in Subacute Sclerosing Panencephalitis: A Case Report and Review of the Literature2
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