The Effects of Digital Health Interventions on Motor Symptoms, Nonmotor Symptoms, and Quality of Life in Patients With Parkinson Disease: Systematic Review and Meta-Analysis of Randomized Controlled Trials.

Hypothalamic atrophy in progressive supranuclear palsy, assessed by convolutional neural network-based automatic segmentation.

Association of Bassoon (BSN) Gene Mutations With Gait and Motor Impairments in Parkinson's Disease.

Self-reporting quality of life in mild-to-moderate Alzheimer's disease and Lewy body dementia: Comparing capability and health-focused measures using response process validation.

CHCHD2 links mitochondrial dysfunction and α-synuclein misfolding in Parkinson's disease.

Familial young-onset Parkinson's disease associated with SNCA gene duplication: a case series of three sisters from Turkey.

Spontaneous tauopathy with parkinsonism in an aged cynomolgus macaque.

Levodopa intolerance as a potential clinical red flag for neuronal intranuclear inclusion disease (NIID) in atypical parkinsonism: a case report.

Real-time detection and subtyping of "On-meds" freezing of gait in Parkinson's disease using lower-limb acceleration data.

Blastocystis hominis infection inducing gut microbiome dysbiosis and aggravating Parkinson's disease symptoms: a case report.

Prompting and Fine-Tuning Large Language Models for Parkinson Disease Diagnosis: Comparative Evaluation Study Using the PPMI Structured Dataset.

Risk factors and outcome of dopamine dysregulation syndrome in a large Chinese Parkinson's disease cohort.

An updated definition of freezing of gait.

Pearls & Oy-sters: Hereditary Spastic Paraplegia Type 15 Presenting as Juvenile Onset Levodopa-Responsive Parkinsonism.

No evidence for the LRRK2 p.L1795F variant in a Southern Italian cohort with Parkinson's disease.

Wernicke's encephalopathy unmasking progressive supranuclear palsy and Alzheimer's pathology: a diagnostic challenge in an older adult.

Zonisamide-induced pleural effusion and agranulocytosis: a case report of a rare adverse reaction.

Akkermansia muciniphila: A double-edged sword in life-stage-specific nutritional modulation of Parkinson's disease via the gut-brain axis.

WES-Based Screening of a Swedish Patient Series with Parkinson's Disease.

Paraneoplastic progressive Supranuclear palsy: a case report and literature review.

Age-Related Differences in the Association between REM Sleep and the Polygenic Risk for Parkinson's Disease.

Computerized cognitive training vs. care as usual to strengthen cognitive, motor, and (neuro)psychological outcomes in people with advanced Parkinson's disease (TrainParC-Advanced): study protocol of a randomized controlled trial.

Bridging pleiotropic mechanisms in leprosy type-1 reactions and neurodegenerative diseases.

Self-delivered arousal-heightening stimuli to improve mobility in persons with parkinsonism: A case series.

Subthalamic DBS-induced diphasic dyskinesias: An overlooked complication?

Assessment of SLC25A46 variants in idiopathic Parkinson's disease.

Current advances in the clinical management of Perry syndrome: is there hope for the future?

Lack of association between G6PD variants and Parkinson disease.

AAV gene therapy for GBA1-related diseases.

NDPACX: a newly defined X-linked Parkinsonian syndrome associated with SLC9A6 hemizygote mutation.

Practices, Resources and Challenges in Parkinson's Disease Management in Asia: Movement Disorders in Asia Study Group Report.

Examination of simple artificial intelligence-based analysis of dopamine transporter scintigraphy for supporting a diagnosis of Parkinson's disease.

A rare case report of acute severe hypokalemia induced by monosialotetrahexosylganglioside therapy.

Advances in the genetics and pathology of Lewy body dementia.

An international 20 country patient and physician survey of the usability and acceptability of Stepped Care pathway in Parkinson's disease.

Successful resolution of Capgras syndrome with rivastigmine treatment in Lewy body dementia.

Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease.

C-terminus-dependent detection of lysosomal alpha-synuclein in nigral Parkinson's disease human brain neurons.

A Variant of OTUD3 in Early-Onset Parkinsonism.

Cerebral amyloid angiopathy-related inflammation superimposed on alpha-synucleinopathies: a case report and literature review.

Toward Biology-Driven Diagnosis of Atypical Parkinsonian Disorders.

Telephone-based cognitive screening in neurodegenerative MCI and dementia: preliminary findings from the TBCS Study.

Parkinson's disease mild cognitive impairment with MRI evidence of cholinergic nucleus 4 degeneration: A new subtype?

Lysosomal Network Defects in Early-Onset Parkinson's Disease Patients Carrying Rare Variants in Lysosomal Hydrolytic Enzyme Genes.

Delayed emergence of parkinson's disease after reversible manganese-induced parkinsonism: a case report.

Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's Disease.

RAB39B Related Parkinsonism in an Italian Family: A Unique Use of Advanced Therapies.

Mutations in the Key Autophagy Tethering Factor EPG5 Link Neurodevelopmental and Neurodegenerative Disorders Including Early-Onset Parkinsonism.

Parkinsonism-Hyperpyrexia Syndrome Following Deep Brain Stimulation Battery Depletion during the COVID-19 Pandemic: A Case Series and Review of the Literature.

A novel alpha-synuclein G14R missense variant is associated with atypical neuropathological features.

Repeat Variants, Biomarkers, and Molecular Signatures in Parkinson's Disease: ATXN2, ATXN3, CACNA1A, PRNP, TBP, C9ORF72, TOMM40, APOE, and POLG-A Swedish Perspective.

Effectiveness of virtual reality rehabilitation with exergames on functional rehabilitation in Parkinson's disease: a systematic review of chronic randomized controlled trials.

Ginsenoside Rk3 Alleviates Neuroinflammation and Gastrointestinal Dysfunction in Parkinson's Disease via Modulation of Gut Microbiota-Mediated Butyric Acid Metabolism.

Moyamoya Disease and the Risk of Parkinson's Disease.

Proteomics of Patient-Derived Striatal Medium Spiny Neurons in Multiple System Atrophy.

In-vivo evidence of synucleinopathy in parkinsonism due to VCP mutation.

Preliminary observations of glucose metabolism dysregulation in pediatric Huntington's disease.

A Novel α-Synuclein K58N Missense Variant in a Patient with Parkinson's Disease.

Homer-3 antibody in autoimmune cerebellar syndromes: a potentially treatable mimic of MSA-C - A review.

Compound Heterozygous Structural Variants in Cases with Unsolved PRKN-Associated Parkinson's Disease.

Prevalence of NOTCH2NLC and FMR1 Repeat Expansions in Atypical Parkinsonism Compared to Asymptomatic Elderly Individuals.

Plasma Markers of Astrocytic and Axonal Integrity in Idiopathic/Isolated REM Sleep Behavior Disorder (iRBD) as Predictors of Dementia with Lewy Bodies.

Association of sustained extremely low income and income decrease with the risk of Parkinson's disease: A population-based nationwide cohort study in Korea.

Genetic analysis of GBA1 gene in a cohort of patients with Parkinson's disease.

The Causal Pivot: A structural approach to genetic heterogeneity and variant discovery in complex diseases.

Development and Characterization of a Novel α-Synuclein-PEST H4 Cell Line for Enhanced Drug Screening in α-Synucleinopathies.

Morphological profiling reveals neuroprotection via mitochondrial uncoupling in human dopaminergic neurons.

Genetically Predict Diet-derived Antioxidants and Risk of Neurodegenerative Diseases Among Individuals of European Descent: A Mendelian Randomization Study.

Tau uptake by human neurons depends on receptor LRP1 and kinase LRRK2.

Computational association in parkinson's disease SNPs with brain structural and functional alterations.

[Sporadic form of Guam disease (ALS-parkinsonism-dementia complex)].

Amyloid fibril structures link CHCHD10 and CHCHD2 to neurodegeneration.

Genetic analysis of TMEM230 variants in Han Chinese patients with Parkinson's disease.

Brain Bleeding Associated With Cavitation During Focused Ultrasound Ablation.

Lysosomal glucocerebrosidase is needed for ciliary Hedgehog signaling: A convergent pathway contributing to Parkinson's disease.

Cognitive outcomes of infusion therapies in Parkinson's disease: A comprehensive systematic review.

The Parkinson Disease-Associated Mutant DNAJC13(N855S) Leads to Its Accelerated Degradation and Negatively Affects Macroautophagy and Retromer Complex-Mediated Dynamics.

Lung function and the risk of Parkinson's disease: a population-based cohort study.

PPM1M, an LRRK2-counteracting, phosphoRab12-preferring phosphatase with a potential link to Parkinson's disease.

The role of blood-based biomarkers in Parkinsonian disorders, Alzheimer's disease and frontotemporal dementia.

Synaptic enrichment of pSer129 alpha-synuclein correlates with dopaminergic denervation in early-stage Parkinson's disease.

Efficacy of various acupuncture modalities on alleviating symptoms in Parkinson's disease: a systematic review and meta-analysis of randomized controlled trials.

Prodromal, established, and advanced Parkinson's disease and atypical parkinsonisms: Prevalence and healthcare service utilization in the Catalan Health Surveillance System (Catpark study).

Engineered Clostridium butyricum-pMTL007-GLP-1 Delays Neurodegeneration in Prnp-SNCA*A53T Transgenic Mice Model by Suppressing Astrocyte Senescence.

Association between alcohol consumption and mortality in Parkinson's disease.

Music-based intervention as a new therapeutic treatment for executive dysfunction in Parkinson's disease.

Loss-of-function coding variants in the Ras of complex proteins/GTPase domain of leucine rich repeat kinase 2.

Exploring GBA1 gene in Parkinson's disease: Prevalence and variant spectrum from Asia minor.

Lewy-MSA hybrid fold drives distinct neuronal α-synuclein pathology.

Differential Effects of Levodopa and Stimulation on Post-Surgery Freezing of Gait in Subthalamic Nucleus Deep Brain Stimulation Parkinson's Disease Patients: A Clinical and Kinematic Analysis.

The compensatory effect of education as revealed by resting-state electroencephalographic alpha rhythms in patients with dementia due to Parkinson's disease: findings from an exploratory study.

ANKK1, ANKRD50, GRK5, PACSIN1 and VPS8 are novel candidate genes associated with late onset Parkinson's disease: Definition of a novel predictive protocol based on polygenic model of inheritance.

Phenotypic Diversity in Stress-induced Childhood-Onset Neurodegeneration with Variable Ataxia and Seizures: Novel Associations with Parkinsonism, Icthyosis and Cataract.

Vascular parkinsonism: an update.

The Genetic Architecture of Parkinson's Disease in Morocco: Highlighting a Predominance of Mendelian Genes.

An Extremely Rare Case of Gastroptosis Treated Successfully with Itopride in a Patient with Parkinson's Disease.

Clinical and genetic characteristics of PLA2G6-related parkinsonism in Southwest China and a comprehensive literature review.

Dyskinesia-Hyperpyrexia Syndrome in Parkinson's Disease May Benefit from GPi Deep Brain Stimulation: A Case Report.

Identifying Common Disease Trajectories of Progressive Supranuclear Palsy with Electronic Health Records.

Early thinking palliative care for people with Parkinson's disease: A thematic synthesis based on a systematic mixed-methods review.

Increased burden of rare risk variants across gene expression networks predisposes to sporadic Parkinson's disease.

Impact of LRRK2 and GBA variants on orthostatic hypotension in patients with Parkinson's disease.

Tics and Parkinson's Disease: Clinical and Pathophysiological Insights from a Rare Syndromic Association.

Concomitant progressive supranuclear palsy and multiple system atrophy: A rare case report of tauopathy and synucleinopathy interface.

Uncovering Important Diagnostic Features for Alzheimer's, Parkinson's and Other Dementias Using Interpretable Association Mining Methods.

Genome-Wide Association Study of Glucocerebrosidase Activity Modifiers.

Deep brain stimulation alleviates Parkinsonian motor deficits through desynchronizing GABA release in mice.

Identification of DAGLB variants in Japanese early-onset Parkinson's disease.

Sidransky Syndrome-GBA1-Related Parkinson's Disease and Its Targeted Therapies.

Parkinson's Spectrum Mechanisms in Pregnancy: Exploring Hypothetical Scenarios for MSA in the Era of ART.

Concomitant Pathologies and Their Impact on Parkinson Disease: A Narrative Overview of Current Evidence.

Optical coherence tomography reveals retinal structural abnormalities in α-synucleinopathies: insights from the Padua-CESNE cohort.

Analysis of intracerebral abscesses in Deep Brain Stimulation and association with hardware-related wound complications.

Co-occurrence of parkinson disease and multiple sclerosis - a critical note.

Exploring Diagnostic Markers and Therapeutic Targets in Parkinson's Disease: A Comprehensive 1H-NMR Metabolomic Analysis - Systematic Review.

Commander complex regulates lysosomal function and is implicated in Parkinson's disease risk.

Biallelic Variants in EPG5 Gene Are Associated with Parkinson's Disease.

Tet2 loss and enhanced ciliogenesis suppress α-synuclein pathology.

Progranulin Mutation Manifesting as Parkinson Disease: A Case Series from the PADUA-CESNE Cohort.

Levodopa induces thyroid function regulation in a patient with thyroid hormone resistance and Parkinson's disease: a case report.

Motor-Cognitive Dual-Task Cost and Associated Micro Lesions of Cerebellum and Brainstem in Multiple System Atrophy (Parkinsonian Type).

Managing impulse control and related behavioral disorders in Parkinson's disease: where we are in 2025?

Neuropsychological Tests of Memory, Visuospatial, and Language Function in Parkinson's Disease: Review, Critique, and Recommendations.

Renaming Twiddler's syndrome: an argument for change to reflect a diverse set of aetiologies, patients and devices.

Unveiling the enigmatic: Primary progressive apraxia of speech - A case report.

Prevalence and Clinical Characteristics of the LRRK2 p.L1795F Variant in Central Europeans with Early-Onset and Familial Parkinson's Disease.

Conversion between NMSS and MDS-NMS in Parkinson's Disease.

Association of waist circumference with all cause mortality in Parkinson's disease.

Recognition, management, and patient perspectives of impulsive-compulsive disorders in Parkinson's disease.

Comprehensive analysis of SLC17A5 variants in large European cohorts reveals no association with Parkinson's disease risk.

Sympathetic and parasympathetic subtypes of body-first Lewy body disease observed in postmortem tissue from prediagnostic individuals.

Neuroprotective role and mechanistic insights of DJ-1 dimerization in Parkinson's disease.

Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson's disease.

Serotype and distribution of adhesion genes in Streptococcus mutans isolated from people with Parkinson's disease.

Paired copy number variation analysis in siblings discordant for familial Parkinson's disease.

Rethinking 'rare' PINK1 Parkinson's disease: A meta-analysis of geographical prevalence, phenotypic diversity, and α-synuclein pathology.

Rare SV2C coding variants in Parkinson's disease risk.

Estimation of and clinical consensus on the meaningful motor progression threshold on MDS-UPDRS Part III.

Does drug repurposing bridge the gaps in management of Parkinson's disease? Unravelling the facts and fallacies.

P2RX7, an adaptive immune response gene, is associated with Parkinson's disease risk and age at onset.

Prevalence and correlates of the head turning sign in mild cognitive impairment and dementia due to neurodegenerative, chronic cerebrovascular, and mixed etiologies.

Early-onset Parkinson's disease in a patient with a rare homozygous pathogenic GBA1 variant and no Gaucher disease symptoms.

Pathomechanisms of neuropsychiatric disturbances in atypical parkinsonian disorders: a current view.

[Parkinson's disease: from genetics to targeted therapies].

Skin calcium deposits in primary familial brain calcification: A novel potential biomarker.

PLA2G6-associated Neurodegeneration: A Rare Case Report of Dystonia-Parkinsonism Phenotype with a Novel Genotypic Variant.

The novel p.A30G SNCA pathogenic variant in Greek patients with familial and sporadic Parkinson's disease.

NPT100-18A rescues mitochondrial oxidative stress and neuronal degeneration in human iPSC-based Parkinson's model.

Distinct subcellular localization of tau and alpha-synuclein in lewy body disease.

Progressive supranuclear palsy: an updated approach on diagnosis, treatment, risk factors and outlook in Mexico.

Association between triglyceride/high density lipoprotein ratio and incidence risk of Parkinson's disease: a population-based cohort study.

Opicapone as adjunct to levodopa in treated Parkinson's disease without motor complications: A randomized clinical trial.

TDP-43 Cryptic RNAs in Perry Syndrome: Differences across Brain Regions and TDP-43 Proteinopathies.

Development and use of DJ-1 affinity microcolumns to screen and study small drug candidates for Parkinson's disease.

Plasma pTau181 and amyloid markers predict conversion to dementia in idiopathic REM sleep behaviour disorder.

Ginsenosides Rg1, Rb1 and rare ginsenosides: Promising candidate agents for Parkinson's disease and Alzheimer's disease and network pharmacology analysis.

A rare variant in the UQCRC1 gene, p.(Gly405Val) in three Austrian Parkinson's patients.

Diagnosis and treatment of autonomic failure, pain and sleep disturbances in Parkinson's disease: guideline "Parkinson's disease" of the German Society of Neurology.

Parkinson disease-associated toxic exposures selectively up-regulate vesicular glutamate transporter vGlut2 in a model of human cortical neurons.

Alpha-synuclein RT-QuIC assay in gastroduodenal and skin biopsies of Parkinson disease patients.

MRI classification of progressive supranuclear palsy, Parkinson disease and controls using deep learning and machine learning algorithms for the identification of regions and tracts of interest as potential biomarkers.

Shared and distinct changes in the molecular cargo of extracellular vesicles in different neurodegenerative diseases.

Early Levodopa-Induced Motor Complications in RAB39B X-Linked Parkinsonism.

The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons.

Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson's disease risk.

Lewy pathology formation in patient-derived GBA1 Parkinson's disease midbrain organoids.

Synaptic and cognitive impairment associated with L444P heterozygous glucocerebrosidase mutation.

Distinct fingerprints of tRNA-derived small non-coding RNA in animal models of neurodegeneration.

Eye movement disorders: A new approach to preliminary screening of Parkinson's disease.

A strategic approach of the management of sleep-disordered breathing in multiple system atrophy.

Tremor Is Highly Responsive to Levodopa in Advanced Parkinson's Disease.

CACHE Challenge #1: Targeting the WDR Domain of LRRK2, A Parkinson's Disease Associated Protein.

Reliable change indices for the Italian version of the Montreal Cognitive Assessment (MoCA) in non-demented Parkinson's disease patients.

Parkinson disease therapy: current strategies and future research priorities.

Recognition and characterising non-motor profile in early onset Parkinson's disease (EOPD).

FIG4-Related Parkinsonism and the Particularities of the I41T Mutation: A Review of the Literature.

Targeted nanopore sequencing using the Flongle device to identify mitochondrial DNA variants.

Rare but relevant: Methamphetamine and Parkinson's disease.

The Black and African American Connections to Parkinson's Disease (BLAAC PD) study protocol.

Perry Disease: Current Outlook and Advances in Drug Discovery Approach to Symptomatic Treatment.

High-throughput screening for small-molecule stabilizers of misfolded glucocerebrosidase in Gaucher disease and Parkinson's disease.

Interplay of α-Synuclein Oligomers and Endoplasmic Reticulum Stress in Parkinson'S Disease: Insights into Cellular Dysfunctions.

Sustained effect of prasinezumab on Parkinson's disease motor progression in the open-label extension of the PASADENA trial.

A rare patient with Parkinson's disease presenting with isolated progressive micrographia.

Pathologically Confirmed Alzheimer's Disease Presenting as Clinical Parkinson's Disease, A Case Report.

Genetic Analysis of Neurite Outgrowth Inhibitor-Associated Genes in Parkinson's Disease: A Cross-Sectional Cohort Study.

Efficacy and safety of riluzole for treating motor function in rare dyskinesia syndromes: a systematic review with meta-analysis.

Association Between Body Mass Index Changes and All-Cause Mortality in Parkinson's Disease.

Combining Biomarkers with Genetics In Prodromal/Earliest Phase Parkinson's Disease.

A case of corticobasal syndrome possibly associated with anti-Yo antibodies.

Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes.

Cerebellar transcranial magnetic stimulation improves motor function in Parkinson's disease.

Progressive gray matter atrophy in parkinsonian variant of multiple system atrophy assessed by using causal structural covariance network.

Fungal Coculture of Herpotrichia sp. and Trametes versicolor Induces Production of Diverse Metabolites with Anti-Parkinson's Neuroprotective Activity.

Exercise Habits in People with Parkinson's: A Multinational Survey.

Akinetic crisis and withdrawal syndromes: guideline "Parkinson's disease" of the German Society of Neurology.

A General Neurologist's Practical Diagnostic Algorithm for Atypical Parkinsonian Disorders: A Consensus Statement.

The akinetic crisis in Parkinson´s disease- the upper end of a spectrum of subacute akinetic states.

Determinants of care partner burden in atypical Parkinsonian syndromes: A retrospective, multi-center analysis.