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 2021-12-01 to 2025-12-01.)
ArticleCitations
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Masquerading as Charcot-Marie-Tooth Disease: A Case Study and Literature Review of Korean Patients32
Retinal Thinning as a Marker of Disease Severity in Progressive Supranuclear Palsy32
Efficacy and Safety of Zolpidem for Musician’s Dystonia32
Sensitivity of Detecting Alpha-Synuclein Accumulation in the Gastrointestinal Tract and Tissue Volume Examined28
Anti-IgLON5-Related Movement Disorders: A Series of Three Cases from a Tertiary Centre in India27
Effect of Chelation Therapy on a Korean Patient With Brain Manganese Deposition Resulting From a Compound Heterozygous Mutation in the SLC39A14 Gene26
The Landscape of Parkinson’s Disease Treatment in India: A National Cross-Sectional Survey of Clinical Practitioners24
Pain Characteristics of Parkinson’s Disease Using Validated Arabic Versions of the King’s Parkinson’s Disease Pain Scale and Questionnaire: A Multicenter Egyptian Study22
The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene20
Investigation of the Long-Term Effects of Amantadine Use in Parkinson’s Disease20
Knowledge, Attitudes and Perceptions of Genetic Testing Among Patients With Movement Disorders, Their Caregivers and Health Care Professionals18
Muscle Dystonia Manifesting as Unilateral Rectus Abdominis Hypertrophy and Abdominal Pain in Parkinson’s Disease: A Case Report14
Congenital ataxic phenotype of ITPR1 -related disorder due to novel missense variants – A video case series14
Evaluating the Validity and Reliability of the Korean Version of the Scales for Outcomes in Parkinson’s Disease–Cognition14
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 Gait12
Validity and Reliability of the Korean-Translated Version of the International Cooperative Ataxia Rating Scale in Cerebellar Ataxia11
Joubert Syndrome Presenting With Levodopa-Responsive Parkinsonism11
The Application of Deep Brain Stimulation in the Syndrome of Irreversible Lithium-Effectuated Neurotoxicity11
Comparing Montreal Cognitive Assessment Performance in Parkinson’s Disease Patients: Age- and Education-Adjusted Cutoffs vs. Machine Learning11
Syringomyelia Manifesting With Pseudodystonia: A Case Report11
High Levels of Mutant Huntingtin Protein in Tear Fluid From Huntington’s Disease Gene Expansion Carriers10
Adult-Onset Genetic Leukoencephalopathies With Movement Disorders8
Optimal Stimulation Sites and Long-term Efficacy of Pallidal Deep Brain Stimulation for Tardive Dystonia8
A Novel Variant of GCH1 in Dopa-Responsive Dystonia With Oculogyric Crises and Intrafamilial Phenotypic Heterogeneity8
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 Report8
Movement Disorders Resulting From Bilateral Basal Ganglia Lesions in End-Stage Kidney Disease: A Systematic Review8
MRI-Guided Focused Ultrasound in Parkinson’s Disease and Essential Tremor: Incisionless but Invasive. A Narrative Review7
Jaw Opening Myoclonus in Subacute Sclerosing Panencephalitis: A New Phenotypic Observation7
Deep Brain Stimulation for Hemiballismus: A Case Report and Review of the Literature7
Association Between Exposure to Particulate Matter and the Incidence of Parkinson’s Disease: A Nationwide Cohort Study in Taiwan7
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
Early-Onset Spastic Ataxia in a Patient With the Prion (PRNP) p.Val180Ile Variant6
Cervical proprioception in Parkinson's disease and its correlation with manual dexterity function6
Historical and More Common Nongenetic Movement Disorders From Asia6
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
Rapid-Onset Dystonia and Parkinsonism in a Patient With Gaucher Disease6
Shoulder Dysfunction in Parkinson’s Disease: Implications of Motor Subtypes, Disease Severity, and Spinopelvic Alignment5
The Clinical Characterization of Blocking Tics in Patients With Tourette Syndrome5
Clinical and Structural Characteristics of NEU1 Variants Causing Sialidosis Type 15
Challenges in Parkinson’s Disease Care—In Light of the COVID-19 Pandemic5
Fecal Calprotectin in Parkinson’s Disease and Multiple System Atrophy5
The First East Asian Patient With Parkinson’s Disease Caused by the A53E SNCA Mutation With Early Progression to Dementia5
Sex and Gender Influence Urinary Symptoms and Management in Multiple System Atrophy5
Apomorphine Monotherapy for Parkinson’s Disease: A Neglected Option?5
Long-Term Outcomes of Deep Brain Stimulation in Pantothenate Kinase-Associated Neurodegeneration-Related Dystonia5
Effect of Positional Changes on Cerebral Perfusion in Parkinson’s Disease Patients With Orthostatic Hypotension5
Copper Deficiency Myeloneuropathy in a Patient With Wilson’s Disease5
Semiautomated Algorithm for the Diagnosis of Multiple System Atrophy With Predominant Parkinsonism5
The Effects of Biofeedback Therapy on Anxiety and Depression in Parkinson’s Disease: A Pilot Study5
Chorea in GRID2 -Related Disorder: Expanding the Phenotypic Spectrum Beyond Cerebellar Ataxia and Tonic Upgaze5
“Face of the Giant Panda” Sign and Bilateral Thalamic Hyperintensity in Isoniazid-Induced Ataxia5
Acute Extrapyramidal Side Effects Following Domperidone Intake in a 48-Year-Old Female Patient: The First Genetic Alteration and Drug Interaction Characterized4
Enriching global perspectives through a regional lens: Recognition, Assessment, and Management of Tardive Dyskinesia in Southeast Asia4
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
Evidence of Inflammation in Parkinson’s Disease and Its Contribution to Synucleinopathy4
A Novel Pathogenic PSEN1 Variant in a Patient With Dystonia-Parkinsonism Without Dementia4
Tremulous Dystonia Due to GNAL Haploinsufficiency Caused by 18p Deletion Syndrome4
Successful Treatment of a Patient With Tremors and Extensive Brain Lesions Using Posterior Subthalamic Area–Deep Brain Stimulation4
Accuracy of Machine Learning Using the Montreal Cognitive Assessment for the Diagnosis of Cognitive Impairment in Parkinson’s Disease4
Brittle Response to Levodopa as a Marker of Parkinson’s Disease Phenotype Characterized by Heavy Motor and Non Motor Burden4
From Evidence to the Dish: A Viewpoint of Implementing a Thai-Style Mediterranean Diet for Parkinson’s Disease4
Extraction of the pull force from inertial sensors during the pull test for Parkinson’s disease: A reliability study4
The Goal Attainment Scale Refines Patient-Centered Expectations in Botulinum Toxin Treatment of Cervical Dystonia4
A Case of AOA2 With Compound Heterozygous SETX Mutations3
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
The Role of Handedness and Extrainstrumental Burdens on the Course of Musicians’ Dystonia3
Evidence-Based Review on Symptomatic Management of Huntington’s Disease3
Oculogyric Crisis as the First Presentation of Biotin-Thiamine-Responsive Basal Ganglia Disease: A Case Report3
Novel Compound Heterozygous Mutations in the SYNE1 Gene in a Taiwanese Family: A Case Report and Literature Review3
Myoclonic Epilepsy of Unverricht and Lundborg in a Filipino Woman3
Wall-Eyed Bilateral Internuclear Ophthalmoplegia Syndrome in a Patient With Progressive Supranuclear Palsy: A Case Report and Literature Review3
Ocular Vestibular-Evoked Myogenic Potential Assists in the Differentiation of Multiple System Atrophy From Parkinson’s Disease3
Subtyping of Parkinson’s Disease by Longitudinal Trajectories of Levodopa Equivalent Daily Dose3
Diagnostic Spectrum in an “Atypical” Atypical Parkinsonism Syndrome Cohort: A Single Center Experience3
Potential Benefits and Perils of Incorporating ChatGPT to the Movement Disorders Clinic3
Non-Motor Fluctuations in Parkinson’s Disease: Underdiagnosed Yet Important3
Clinical and Pathological Features of CSF1R-Related Disorder Associated with the p.R777Q Pathogenic Variant3
Diagnosing Cerebrotendinous Xanthomatosis in a Middle-Aged Woman With Cervical Dystonia3
Revisiting the Triglyceride–Glucose Index in Parkinson’s Disease: Risk Ractor or Disease Marker?3
Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese Ancestry3
Deep Brain Stimulation for Cockayne Syndrome-Associated Movement Disorder3
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