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Congress
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2024 Case Study / Case Report Abstracts

Poster Hall (Exhibit Hall A)
10:00 - 17:30

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Saturday, September 28
1- Brain De-Ironization with Nasal Spray of Iron Chelator in Treatment of Multiple System Atrophy, a Case Trial
14- Role of the Alpha-synuclein Seed Amplification Assay in Parkinson’s Disease Clinical Trials: A Case Report of Multiple System Atrophy Misdiagnosed as Parkinson’s Disease
22- Multiple System Atrophy in a Patient with Normal Pressure Hydrocephalus
30- Lyme disease presenting as a rapidly progressive MSA-C look alike
36- Familial Multiple System Atrophy-Mimics: Importance of Comprehensive Evaluation
37- Heterogeneity of multiple system atrophy with an analysis of the clinical case
38- Posterior Fossa Arachnoid Cysts In Two Patients With Suspected Multiple System Atrophy – Cerebellar Type
50- Paraneoplastic neurological syndrome mimicking a progressive supranuclear palsy: a case series
77- Progressive freezing of gait in atypical parkinsonism. A Possible Progressive Supranuclear Palsy phenotype.
78- PSP: a Clinical Case
80- Pisa Syndrome as an early presenting feature of Corticobasal Ganglionic degeneration [CBGD]
82- Stiff Person Syndrome developing into Corticobasal Syndrome: a case report.
106- Preventing Treatment Disruptions: The Crucial Role of Outpatient Nurses and Multidisciplinary Collaboration in Managing Skin Complications during Foslevodopa/Foscarbidopa Therapy
133- A case of progressive supranuclear palsy followed by dementia with Lewy bodies
135- A Case of Concurrent Wilson Disease and Parkinson Disease
140- Trihexyphenidyl Use in a Parkinsonian Phenotype of Gerstman-Sträussler-Scheinker Syndrome
143- Early-onset Parkinsonism as Presenting Manifestation of CADASIL in a Mexican Woman with NOTCH3 c.1732C>T Pathogenic Variant
145- Perry Syndrome due to a DCTN1 novel variant
149- Pallidotomy as a Therapeutic Option for Patients with Advanced Parkinson's Disease: Case Study
166- Case Report: An Unusual Case of Corticobasal Syndrome
177- Characterization of Autoimmune Parkinsonism. A case series
180- Delayed Parkinsonism as a Delayed Neurological Sequele in Carbon Monoxide Intoxication: A Rare Case Report
182- PSP-Like Syndrome Associated with Dysautonomic Findings as a Presentation of an Anti-Iglon5 Antibody-Related Encephalopathy
183- Giant Aneurysm Causing Parkinsonism and REM Sleep Disorder
190- Atypical Parkinsonism Secondary to Recurrent Deep Vein Thrombosis with Associated Intracranial Dural Fistula
191- Normal pressure hydrocephalus in two Parkinson’s disease patients with deep brain stimulation – co-occurrence or complication
192- Subdural Hematoma Leading to Subacute Secondary Parkinsonism
193- Parkinsonism Associated with Twinkle Gene Mutation
194- Unique Presentation of SPG 15 as Juvenile Levodopa Responsive Parkinsonism: A Case Report
195- Parkinsonism due to Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (ALSP) Responsive to Carbidopa/Levodopa
204- The course of cognitive impairment in Parkinson's disease patients with Сovid-19
212- Wilson Disease Presenting as Rapidly Progressive Dementia
316- Molecular Landscape of Gastrointestinal Dysfunctions in Parkinson's Disease
325- Prevalence of Autonomic Symptoms in Mexican Population with Parkinson's Disease
333- Impairment of REM Sleep Architecture: A Potential Biomarker for Parkinson's Progression
363- Plasma NFL predicting fatigue conversion in early Parkinson’s disease
384- Reduced Thalamic Nuclei Volume May Contribute to Anxiety in Parkinson’s Disease: a 7-Tesla MRI Study
389- Gender-related Cognitive Disparities in Hispanic Patients with Parkinson's Disease: A Cross-Sectional Study
404- Dopamine agonist use and psychotic symptoms in patients with Parkinson’s disease.
413- Cognitive load in a diagnostic electrophysiologic assessment of functional tremor.
416- The Role of Cortisol  a Mediator in Influencing Cognitive Function
425- Complete Resolution of Tardive Dystonia After Bilateral Globus Pallidus Interna Deep Brain Stimulation
426- Reversing the irreversible: The application of Deep Brain Stimulation in The Syndrome of Irreversible Lithium Effectuated Neurotoxicity.
429- Quantitative EEG Analysis for Comparing Drug-Induced Parkinsonism and Parkinson's Disease
431- Bistriatal hypermetabolism on 18-FDG PET-CT in tardive dyskinesia
432- Tardive Dystonia Following Risperidone Treatment :  A Case Report and Therapeutic Approach
433- Acute dystonic dyskinesias in a patient used fluvoxamine. Case report
434- Central Tremor after CAR-T Cell Therapy: A Case with Neurophysiologic Characterization
437- Prevalence of Movement Disorders in Epilepsy Patients Taking Antiepileptics Drugs in a Tertiary Care Teaching Hospital in Nepal.
438- Comorbid Tardive Dyskinesia (TD) and Restless Leg Syndrome (RLS)
439- Oro-facial Dyskinesia and akathisia following Treatment by Olanzapine
440- Rare Clinical Manifestation of Tardive Dyskinesia In Schizophrenic Patient on Quetiapine and Sertraline: A Case Report
496- Depression and Cognitive Phenotype in Idiopathic Parkinson's Disease without Dementia (IPDWD). Preliminary Results of a Comparative Study of a New Scale ESDEPARK Assessing Depressive Symptomatology Specifically in IPDWD vs a General Geriatric Depression S
504- Enhancing Real-Life Gait Performance in Persons with Parkinson Disease through the Music-Based BeatWalk Application
541- Long-term Physical Exercise on Bone Mineral Density, Balance and Gait in Older Adults with Mild to Moderate Parkinson's Disease
600- Parkinson’s Disease (PD) and predictors of Driving Cessation: Results from a 6-year Longitudinal Study and a systematic review of the literature
603- "Quality of Life of Caregivers Living with a Movement Disorder. A Comprehensive Approach."
Sunday, September 29
641- Essential3: An Innovative Multi-Study Phase 3 Program to Evaluate the Efficacy and Safety of Ulixacaltamide
651- Differential Symptom Cluster Responses and Predictors to Repetitive Transcranial Magnetic Stimulation Treatment in Parkinson’s Disease:A Retrospective Study
765- Assessment of Motor and Non-Motor Alterations Impacting Functionality in Parkinson's Disease Patients
785- Design, synthesis and pharmacological evaluation of 16-pyridylmethylene derivatives of steroidal oximes as antiparkinsonian agents in MPTP-injected mice.
812- Association between Fecal Bile Acids and Levodopa Response in Patients with Parkinson’s Disease
816- Attitudes and Beliefs Towards Medication Burden and Deprescribing in Parkinson Disease
830- Adherence and Persistence Among Patients with Parkinson’s Disease Initiating Istradefylline: 12-Month Follow-Up from US Real-World Data
881- Association between statin use and mortality in Parkinson’s disease
882- A case of malignant Deep Brain Stimulation Withdrawal Syndrome treated with Opicapone
883- ECAP-Controlled Closed-Loop SCS Alleviates Neuropathic Pain and Improves Motor Function in a Patient Suffering from Parkinson’s Disease and Radicular Pain
884- Peri-Electrode Edema after Deep Brain Stimulation Implantation – Case Report and Literature Review
972- Essential Tremor: The Relationship Between Hand Dominance and Tremor Severity by MVPA
975- Neuroimaging Factors Differentially Associated with Pathology and Clinical Presentation
1043- Severity of Motor Symptoms Correlates with Asymmetric Changes in Globus Pallidus Internus and Caudate Nuclei in Parkinson’s Disease
1084- Comparative Study of Whole-Brain Functional Connectivity Patterns in Parkinson's Disease and Essential Tremor: A Resting-State fMRI Study
1090- Alterations in neural processes of cognitive control in asymptomatic heterozygous mutation carriers in the Parkin gene
1092- Emergency pallidotomy in a patient with chorea paralytica in primary hypoparathyroidism
1093- Cognitive Outcome in Pantothenate Kinase-Associated Neurodegeneration (PKAN) Treated with Deep Brain Stimulation (DBS):Case Report
1094- One-Year Outcomes of Multitarget Thalamic and Pallidal Deep Brain Stimulation in Unilateral Dystonia
1095- Deep Brain Stimulation (DBS) Improves Parkinsonism Caused by Osmotic Demyelination Syndrome (ODS)
1096- Pregnancy in Dystonia or Tourette’s patients with DBS. Eleven New Cases and a Review of the Literature.
1099- Real-World Clinical and Safety Outcomes from a Prospective, Multicenter Deep Brain Stimulation Registry of Essential Tremor Patients
1101- Impact on quality of life and nonmotor symptoms of unilateral magnetic resonance-guided focused ultrasounds (FUS) thalamotomy in patients with essential tremor.
1102- Deep Brain Stimulation of bilateral ventral intermediate nucleus in a patient with spinocerebellar ataxia type 12
1109- Botulinum Toxin and Deep Brain Stimulation in Dystonia
1115- Unveiling the Long-term Impact of Unilateral Vim DBS in Essential Tremor
1119- Deep brain stimulation of globus pallidus internus for monogenic dystonia
1120- GNAO1-related Neurodevelopmental Disorder with Involuntary Movements Inducing a Dyskinetic Status
1121- Acute Reversible Laughter with Globus Pallidus Interna Stimulation
1122- Vim DBS for Post-Stroke Tremor: A Case Report
1123- Deep brain stimulation of bilateral ventral intermediate nucleus in patients with neuronal intranuclear inclusion disease
1125- Intraoperative venous air embolism in the semi-sitting position in functional neurosurgery
1127- The Characteristics and Management of Patients with Dystonia Referred for The Troubleshooting of Deep Brain Stimulation Therapy: A Single Center Experience
1128- Holmes Tremor Treated with Pallidal Stimulation
1168- Effect of Target Selection on Mood, Pain, and Medications after DBS in PD
1173- Functional connectivity enhances prediction of STN DBS motor outcomes
1176- Longevity of Motor Benefit Achieved with Deep Brain Stimulation (DBS) of the Subthalamic Nucleus (STN) in a Single Center Cohort at the Decade Mark Post-Implantation.
1181- Early Outcomes Support use of a Remote Cross-Border Surgical Centre for Deep Brain Stimulation in Parkinson’s Disease
1186- The Challenges of Adaptive Deep Brain Stimulation: A Delphi Panel Study
1254- Identification of Fall Risk in Patients with Parkinson's Disease Through Telemonitoring
1259- Digital health technology (DHT) derived features as sensitive measures of disease progression in early Parkinson’s disease under stable dopaminergic treatment
 Monday, September 30 
1280- Spectrum of polysomnographic abnormalities in a cohort of sporadic late onset ataxia patients
1282- White Matter Tractography in Spinocerebellar Ataxia type 1 and 2 in comparison with Healthy Controls
1283- Variant Ataxia Telangiectasia: A Novel ATM Gene Mutation With Disabling Tremor and Response to Deep Brain Stimulation
1284- Novel Partial Gene Deletion in CaCNA1A Presenting with Gait Ataxia, Vertigo, and Abnormal Eye Movements
1286- Increased Risk of Suicidal Ideation in Patients with Spinocerebellar Ataxias
1289- Spinocerebellar ataxia type 2 (SCA2) and Seizures: Is There a Correlation?
1291- Progressive Myoclonic Ataxia: Neuroinflammation and Autoantibodies Against Inhibitory Synapses and Herpes Viruses
1294- Pulmonary Dysfunction in Friedreich's Ataxia (FRDA)
1298- Association of expanded CAG repeat with autonomic function in Spinocerebellar Ataxia Type-2 (SCA-2)
1300- Clinical and Genetic Profile of Spinocerebellar Ataxias in a Tunisian Cohort
1302- Prevalence of Heterozygous ATP7B Mutation in Patients with Movement Symptoms
1305- Electrophysiological study of 122 Tunisian patients with autosomal recessive cerebellar ataxia
1307- NGS diagnosis rate in a combined cerebellar ataxia and spastic paraplegia series from southern Spain
1311- Substantia Nigra Degeneration In Spinocerebellar Ataxia 2 And 7 Using Neuromelanin-Sensitive Imaging
1312- Ataxia, tremor, fasciculations and hemiparesis in a GBA1 heterozygous female carrier
1314- Oculomotor Biomarkers for Cerebellar Ataxia and Severity in Smooth Pursuit
1316- Alterations in the Daily Living Gait and Mobility during the Day and Night among Individuals with Cerebellar Ataxia, SCA3: An Exploratory Study
1317- Spinocerebellar Ataxia Type 49 presenting with Early onset Dystonia-Ataxia in an Indian Female
1324- Predicting Disease Severity in Friedreich's Ataxia through Wearable Monitoring and Machine Learning.
1325- CAPRIN1 defect: a new severe neurodegenerative disorder with childhood dementia, myoclonus-ataxia, and sensorimotor neuropathy
1328- paraneoplastic cerebellar ataxia: a rare cause of late-onset ataxia
1330- Effects of Transpinal Magnetic Stimulation (TsMS) in Patients Diagnosed with Spinocerebellar Ataxia 3 (SCA 3)
1331- Seminoma resulting in rapidly progressive cerebellar syndrome with associated dual positive kelch-like protein 11 (KLHL11) IgG and leucine zipper 4 (LUZP4)–immunoglobulin G (IgG) antibodies.
1332- Superficial siderosis; a case review
1333- Diagnostic challenges with novel SCA variants: A case of STUB1 mutation
1334- Spastic Ataxia Associated with Congenital Myasthenia Related to the VAMP1 Gene: Report of an Affected Family in Brazil.
1335- Transcranial Direct Current Stimulation and Neurofunctional Physical Therapy Improves Motor and Cognitive Symptoms in a Patient with Type 1 Spinocerebellar Ataxia – A Case Report
1336- Movement disorders secondary to neurocysticercosis: a  case report from Bolivia
1338- Volatile solvent abuse and Cerebellar ataxia: A case series
1340- Friedreich’s ataxia: A descriptive study of a Tunisian cohort
1341- Progressive cerebellar ataxia in primary Sjögren’s syndrome: a case report
1343- A study on the phenomenological analysis of Spinocerebellar Ataxia type 12 revealing a dystonic imprint
1350- Ektacytometry in Neuroacanthocytosis
1351- A Novel Mutation of NKX2-1 Gene: A Rare Presentation of Chorea
1355- The clinical features, neuroimagings and outcomes of diabetic striatopathy: a retrospective study at tertiary hospital in Vietnam
1358- Spectrum of Non-HD Hereditary Chorea- Case Series from An Indian Movement Disorder Centre
1360- A Rare Case of Hemicorea Secondary to Giant Perivascular Space: A Case Report
1361- Clonazepam as First-Line Therapy for Post-Hypoxic Chorea: A Case Report and Discussion
1363- Chorea Acanthocytosis Misdiagnosed as Functional Movement Disorder
1364- Bilateral Fronto-Temporal Lobar Atrophy: An Atypical Magnetic Resonance Imaging Finding in Neuroacanthocytosis
1365- Hyperkinetic Movements Related to COVID-19 Vaccine
1366- Fahr's Disease Presenting as Chorea: A Rare Case Report
1367- Reversible Hemichorea-Hemiballismus-Hemifacial Spasm in Diabetic Striatopathy
1368- Choreoacanthocytosis: The First Genetically Confirmed Cases From Algeria
1369- Cortical Pencil Lining in Brain MRI of a Patient with Chorea and Hepatic Cirrhosis
1370- Acute Chorea in The Emergency Department Related to Systemic Lupus and Antiphospholipid Syndrome: A Case Report
1371- Diabetic striatopathy with stroke - like symptoms: A case report
1372- Severe chorea, ballistic and dystonic movement disorder due to intracerebral hemorrhage in subthalamic nucleus
1379- The Impact of Standardized Recommendations on the Management of Initial and Refractory Pediatric Status Dystonicus
1382- Deep Brain Stimulation in Dystonia: Investigating Differential Response by Dystonia Distribution
1388- Do Lower Doses of Botulinum Neurotoxin Type-A Offer a Longer Duration of Effect and Superior Efficacy in Patients with Cervical Dystonia?
1404- Real-World Diagnosis of Chronic Migraine in Patients With Cervical Dystonia Analyzed by Botulinum Neurotoxin Treatment Exposure: an Epidemiologic Perspective
1406- KMT2B-Related Dystonia And DBS: Tertiary Center Experience
1407- Clinical Outcomes and Local Field Potential Characteristics in Bilateral GPi DBS in 2 cases of X-Linked Dystonia Parkinsonism
1409- Clinical Characteristics and Management Practices of Pediatric Status Dystonicus
1410- Genetic Variant in the VPS16 Gene in a 44-year-old Patient with Generalized Dystonia
1417- Cervical dystonia after cerebellar stroke and medullary hemorrhage
1418- Challenges in Wilson disease management in a resource-limited country: a case report from a tertiary center
1420- Oromandibular Dystonia in Hashimoto Encephalopathy: An Unusual Association Not To Miss
1422- Expanding the concept of “occupational dystonia”: data from the Italian Dystonia Registry
1431- Increased cerebellar grey matter in writer’s cramp patients: a morphometric signature of symptom compensation
1435- Writing dysfluency associates with basal ganglia network dysfunction in writer’s cramp dystonia
1466- Treatment Effect Sizes of Once-Daily Valbenazine for Tardive Dyskinesia and for Chorea Associated with Huntington’s Disease: A Post-Hoc Analysis of Phase 3 Clinical Trial Data
1484- The Spectrum of Presenting Phenotypes in Childhood Onset Huntingtons Disease
1486- Closed-Loop Spinal Cord Stimulation: A Case Report on a Novel Therapeutic Approach for Post-Hypoxic Myoclonus
1487- Treatment of Post-hypoxic Myoclonus using Bilateral Subthalamic Nuclei Deep Brain Stimulation
1490- Cortical myoclonus in DHDDS: the multifaced presentation of a single movement disorder
1492- Mechanism Study of Familial Cortical Myoclonic Tremor with Epilepsy Type 1 Caused by Pentanucleotide Repeat Expansion in the SAMD12 Gene
1493- Childhood onset progressive myoclonus and ataxia in a patient with novel TBC1D2B gene mutation
1502- Benzodiazepines in the Management of Restless Legs Syndrome: A Systematic Review and Meta-Analysis
1522- Ultrasound Assessment of Collagen Content in Contracted and Non-contracted Muscle Areas: A Comparative Study
1533- Contribution to Efficacy by Active Metabolites of Suvecaltamide in a Preclinical Rat Model of Essential Tremor
1546- Dentato-Rubro-Thalamic Tract Deep Brain Stimualtion for Essential Tremor: Stimulation Parameters and Clinical Outcomes
1559- Prevalence of Phosphorylated Alpha-Synuclein in Skin Biopsies of Essential Tremor Patients
1564- Sleep profiles in patients with Essential Tremor and Essential Tremor Plus: Polysomnography Insights
1573- Evaluating the Effect of Myofascial Release on Parkinson's Related Tremor
1576- Is essential tremor-plus phenotype a prodromal phase of Parkinson’s disease ?
1580- Application of Neurophysiology in the Clinical Evaluation of Pediatric and Adolescent Patients with Tremor
1581- Movement Disorders Associated with Infectious Encephalitis in Pediatric Patients
1587- Identification and Screening of Candidate Genes for Paroxysmal Movement Disorders by Next Generation Sequencing Approach for Developing Molecular Diagnostics.
1589- Improving Work Up amongst Patients with Rare Movement Disorders according to Diagnostic Yield Findings– Update from Single Center Neurogenetic Clinic
1595- Three-Year Progression of the Postural Control Alterations in Hereditary Spastic Paraplegias
1597- Expanding the phenotypic spectrum of movement disorders in 22q11.2 deletion syndrome
1598- A Novel SLC9A1 Mutation Associated with Cerebellar Ataxia and Sensorineural Hearing Loss
1599- Parkinsonism in combined Fragile X and XYY Syndromes: A Case Report
1600- Clinico- radiological profile of four patients with CSF1R- related leukoencephalopathy: A case series from India
1604- Intermediate Expansion of MARCHF6 causes FAME3 without Epilepsy
1606- Validation of Inertial Measurement Units and an application compared with the reference system to assess the gait in hereditary spastic paraplegia
1607- OPTN gene associated with corticobasal syndrome: a novel multi-exon deletion and literature review
1619- Association of Gaucher-related and Parkinson’s-private GBA1 variants with progression of PD: A longitudinal mixed model analysis.
1629- Disease Progression in Patients with PLA2G6-related Parkinsonism: A Longitudinal Study
1636- Differences in Oculometric Measures between Patients with LRRK2-associated and Idiopathic Parkinson’s Disease
1668- Genetic Analysis of Mendelian mutations in A Large Chinese Early-onset and Familial Parkinson’s Disease
1681- The Black and African American Connections to Parkinson’s Disease Study
1692- The association of Severity and Monogenetic Subgroups in Parkinson's Disease
1693- 7year followup of Asia’s first case of sporadic ATP6AP2 Mutation: α-synucleinopathy or tauopathy?
1694- Expanding Phenotype of LRRK2 G2019S Mutation: Case Description of Two Sisters Showing Peculiar Phenomenological Traits
1695- A Case of Paradoxical Gait Response to Levodopa in Parkin-Gene-Related Early-Onset Parkinson's Disease
1696- Adding Parkinsonism to the Phenotypic Spectrum of FIG4-related diseases
1697- A new phenotype-genotype correlation for FIG4 gene and Parkinson's disease
1700- Novel ASO Targeting IGHMBP2 Cryptic Splice Variant: Efficacy and Safety
1703- Wilson's Disease : A Senegalese Series of Seven Patients Followed at Pikine National Hospital Centre (Dakar-Senegal)
1704- DPPX Autoimmune Encephalitis Associated with Severe Multifocal Dystonia.
1705- A Patient with Overlapping SPG7 mutation and MERRF
1712- Association between Hyperglycemic Crisis Severity and Movement Disorders in Hispanic Patients with De Novo Hyperglycemia: A Cross-Sectional Study
1725- Mutation of the ATP5F1A gene associated with dystonia, spasticity, myoclonus, cognitive impairment and epilepsy –  a rare case report of a patient
1727- Movement Disorders in Cerebrotendinous Xanthomatosis
1729- Movement Disorders in De Novo Hyperglycemic Crisis: Insights from a Clinical Case Series
1730- A Unique case of Ataxia, Neuropathy, and chronic cough: CANVAS
1731- Startle Reflex in CTNNB1 Mutations: A diagnostic Clue
1732- Dopa-responsive ataxia with compound heterozygous variants in MRE11
1733- Phenotypic variability of mitochondrial tRNA Ser(UCN) gene [MTTS1] mutation: First report from India
1734- PMM2 mutation
1735- Spastic Ataxia and Motorneuron disease as possible manifestations of ATP13A2 (PARK 9) variants
1736- Phenomenology of Coenzyme Q10-deficiency Spinocerebellar Ataxia: Case Description Of Two Siblings And New Therapeutic Perspectives
1743- Complexity of fractal patterns in motor cortical oscillatory activity in rodent models of Parkinson disease
1754- Clinical, Neurophysiological, and Biological Insights into Levodopa-Induced Dyskinesias
1764- Correlation of Neural Sensing with the Volume of Neural Activation within the Desired Patient-Specific Anatomical Target in Deep Brain Stimulation for Parkinson’s Disease
1765- Levels of change in interleukin-6 levels according to clinical forms of Parkinson's disease in patients with and without Covid-19
1770- Quantification of an Upper Limb Rigidity Network in Parkinson Disease
1821- Pregnancy and delivery in women with Parkinson’s disease:  A case series
1844- Free-Viewing Eye Tracking and the Effect of Levodopa in Parkinson’s Disease
1845- Evaluation of unsteadiness in patients with dystonia
1849- Apraxia of eyelid opening in patients with movement disorders
1862- Engage, Educate and Empower: Parkinson’s Research Advocates from the Black and African American Community
1880- Behind the Prison Gates - Creating a nurse led Parkinson’s healthcare pathway at HMP Dartmoor Prison, UK.
1889- Antibody-mediated movement disorders: a single-centre retrospective study
1901- Movement Disorders in the Emergency:New Insights
1905- Tremors Vs. Tremors: the first music album from Parkinson’s tremors
1909- Seeking Traditional Healers in Movement Disorders: a pilot study in two African Countries
1915- Demographics of Botulinum toxin therapy population representative to demographics in Essex County, USA
1916- Dandy-Walker syndrome. A case study.
1917- Wilson's Disease About A Complex Case
1922- PD Young Ambassadors: A Peer-led, Community-Based Intervention to Raise PD Awareness in the Hispanic Communities of Chicago.
1923- Adult Onset Spastic Paraplegia in TUBB4A Leukodystrophy