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 2021-06-01 to 2025-06-01.)
ArticleCitations
Sensitivity of Detecting Alpha-Synuclein Accumulation in the Gastrointestinal Tract and Tissue Volume Examined28
Retinal Thinning as a Marker of Disease Severity in Progressive Supranuclear Palsy25
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
The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene19
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Masquerading as Charcot-Marie-Tooth Disease: A Case Study and Literature Review of Korean Patients19
Investigation of the Long-Term Effects of Amantadine Use in Parkinson’s Disease18
Evaluating the Validity and Reliability of the Korean Version of the Scales for Outcomes in Parkinson’s Disease–Cognition17
Knowledge, Attitudes and Perceptions of Genetic Testing Among Patients With Movement Disorders, Their Caregivers and Health Care Professionals15
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
DHDDS Mutation: A Rare Cause of Refractory Epilepsy and Hyperkinetic Movement Disorder14
Dystonic Opisthotonus in Kufor-Rakeb Syndrome: Expanding the Phenotypic and Genotypic Spectrum13
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
Comparing Montreal Cognitive Assessment Performance in Parkinson’s Disease Patients: Age- and Education-Adjusted Cutoffs vs. Machine Learning11
Joubert Syndrome Presenting With Levodopa-Responsive Parkinsonism11
Syringomyelia Manifesting With Pseudodystonia: A Case Report11
High Levels of Mutant Huntingtin Protein in Tear Fluid From Huntington’s Disease Gene Expansion Carriers10
Movement Disorders Resulting From Bilateral Basal Ganglia Lesions in End-Stage Kidney Disease: A Systematic Review10
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
Historical and More Common Nongenetic Movement Disorders From Asia10
The Application of Deep Brain Stimulation in the Syndrome of Irreversible Lithium-Effectuated Neurotoxicity10
Association Between Exposure to Particulate Matter and the Incidence of Parkinson’s Disease: A Nationwide Cohort Study in Taiwan9
A Novel Variant of GCH1 in Dopa-Responsive Dystonia With Oculogyric Crises and Intrafamilial Phenotypic Heterogeneity9
Jaw Opening Myoclonus in Subacute Sclerosing Panencephalitis: A New Phenotypic Observation8
Adult-Onset Genetic Leukoencephalopathies With Movement Disorders7
Does Restless Legs Syndrome Have a Different Pathomechanism in Premotor and Motor Parkinson’s Disease?7
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
“Face of the Giant Panda” Sign and Bilateral Thalamic Hyperintensity in Isoniazid-Induced Ataxia6
Fecal Calprotectin in Parkinson’s Disease and Multiple System Atrophy6
Efficacy of levodopa/benserazide dispersible tablet on the ‘Delayed-ON’ to first morning dose in patients with Parkinson’s disease with motor fluctuations: a multicenter, randomized, open-label, cross6
Reliability and Validity of the Embouchure Dystonia Severity Rating Scale6
Effect of Positional Changes on Cerebral Perfusion in Parkinson’s Disease Patients With Orthostatic Hypotension6
Rapid-Onset Dystonia and Parkinsonism in a Patient With Gaucher Disease6
Copper Deficiency Myeloneuropathy in a Patient With Wilson’s Disease5
The Clinical Characterization of Blocking Tics in Patients With Tourette Syndrome5
Ataxia and Myoclonus with a Cherry-Red Spot Unfurling an Unusual Phenotypic Presentation of Sialidosis Type 15
Comment on “A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome”5
Semiautomated Algorithm for the Diagnosis of Multiple System Atrophy With Predominant Parkinsonism5
Sex and Gender Influence Urinary Symptoms and Management in Multiple System Atrophy5
Shoulder Dysfunction in Parkinson's Disease: Implications of Motor Subtypes, Disease Severity, and Spinopelvic Alignment5
The First East Asian Patient With Parkinson’s Disease Caused by the A53E SNCA Mutation With Early Progression to Dementia5
Challenges in Parkinson’s Disease Care—In Light of the COVID-19 Pandemic5
Apomorphine Monotherapy for Parkinson’s Disease: A Neglected Option?5
Evidence of Inflammation in Parkinson’s Disease and Its Contribution to Synucleinopathy4
Long-Term Outcomes of Deep Brain Stimulation in Pantothenate Kinase-Associated Neurodegeneration-Related Dystonia4
Accuracy of Machine Learning Using the Montreal Cognitive Assessment for the Diagnosis of Cognitive Impairment in Parkinson’s Disease4
A Novel Pathogenic PSEN1 Variant in a Patient With Dystonia-Parkinsonism Without Dementia4
Acute Extrapyramidal Side Effects Following Domperidone Intake in a 48-Year-Old Female Patient: The First Genetic Alteration and Drug Interaction Characterized4
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
Clinical and Structural Characteristics of NEU1 Variants Causing Sialidosis Type 14
Extraction of the pull force from inertial sensors during the pull test for Parkinson’s disease: A reliability study4
Tremulous Dystonia Due to GNAL Haploinsufficiency Caused by 18p Deletion Syndrome4
Novel Compound Heterozygous Mutations in the SYNE1 Gene in a Taiwanese Family: A Case Report and Literature Review3
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
Adjustability of Gait Speed in Clinics and Free-Living Environments for People With Parkinson’s Disease3
Myoclonic Epilepsy of Unverricht and Lundborg in a Filipino Woman3
Potential Benefits and Perils of Incorporating ChatGPT to the Movement Disorders Clinic3
Chorea as a Presentation of SARS-CoV-2 Encephalitis: A Clinical Case Report3
Diagnosing Cerebrotendinous Xanthomatosis in a Middle-Aged Woman With Cervical Dystonia3
Deep Brain Stimulation in Advanced Parkinson’s Disease: An Uncommon Case of Allergic Encephalitis3
Non-Motor Fluctuations in Parkinson’s Disease: Underdiagnosed Yet Important3
A Case of AOA2 With Compound Heterozygous SETX Mutations3
Oculogyric Crisis as the First Presentation of Biotin-Thiamine-Responsive Basal Ganglia Disease: A Case Report3
Movement Disorders Associated With Radiotherapy and Surgical Procedures3
A Practical Guide for Diagnostic Investigations and Special Considerations in Patients With Huntington’s Disease in Korea3
The Goal Attainment Scale Refines Patient-Centered Expectations in Botulinum Toxin Treatment of Cervical Dystonia3
Deep Brain Stimulation for Cockayne Syndrome-Associated Movement Disorder3
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