Evidence
Mov Disord Clin Pract. 2024 May 2. doi: 10.1002/mdc3.14058. Online ahead of print.
NO ABSTRACT
PMID:38698554 | DOI:10.1002/mdc3.14058
Estimated reading time: 1 minute(s)
Latest: Psychiatryai.com #RAISR4D Evidence
Cool Evidence: Engaging Young People and Students in Real-World Evidence
Real-Time Evidence Search [Psychiatry]
AI Research
Correction to “Gerstmann-Straussler-Scheinker Disease Presenting as Late-Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology”
🌐 90 Days
AI Virtual Reality Related Evidence Matrix
- BCL11B-Related Dystonia: Further Evidence of an Emerging Cause of Childhood-Onset Generalized Dystonia
- Parkinson's Disease Associated with G2019S LRRK2 Mutations without Lewy Body Pathology
- Understanding Anxiety in Cervical Dystonia: An Imaging Study
- Clinical and Pathological Features of FTDP-17 with MAPT p.K298_H299insQ Mutation
- Motor Complications in Parkinson's Disease: Results from 3343 Patients Followed for up to 12 Years
- Improving Conversations about Parkinson's Dementia
- Levodopa-Induced Dyskinesias are Frequent and Impact Quality of Life in Parkinson's Disease: A 5-Year Follow-Up Study
- Deep Brain Stimulation for Orthostatic Tremor: An Observational Study
- Genetic and pathological features encipher the phenotypic heterogeneity of Gerstmann-Sträussler-Scheinker disease
- A New Definition of Psychosis Is Needed in Parkinson's Disease
- Novel PANK2 Variant in Asian Indians with Atypical Pantothenate Kinase Associated Neurodegeneration
- Localized Changes in Dentate Nucleus Shape and Magnetic Susceptibility in Friedreich Ataxia
- Correction to "Comparing randomized controlled trials of outpatient family-based or inpatient multimodal treatment followed by outpatient care in youth with anorexia nervosa: Differences in populations, metrics, and outcomes"
- A life lost to anorexia nervosa: A case report of rapid progressive disease and its psychological aspects
- Neuropsychology of late-onset epilepsies
- Ma2 antibody-associated limbic encephalitis: The early etiology treatment may modify the disease clinical trajectory
- Steroid responsive encephalopathy associated with autoimmune thyroiditis (SREAT) presenting as subacute psychosis: Case report and literature review
- Novel method for classification of prion diseases by detecting PrPres signal patterns from formalin-fixed paraffin-embedded samples
- Gerstmann Syndrome Case-Control Study: Correlation between Brain Lesions & Functional Disability
- Impact of Magnetic Resonance Imaging Markers on the Diagnostic Performance of the International Parkinson and Movement Disorder Society Multiple System Atrophy Criteria
- Correction to "The effect of noninvasive brain stimulation on anhedonia in patients with schizophrenia and depression: A systematic review and meta-analysis"
- Content Validity of the Modified Functional Scale for the Assessment and Rating of Ataxia (f-SARA) Instrument in Spinocerebellar Ataxia
- Content Validity of the Modified Functional Scale for the Assessment and Rating of Ataxia (f-SARA) Instrument in Spinocerebellar Ataxia
- Electrical stimulation mapping guides individualized surgical approach in an epilepsy-associated tumor within language representing cortex
- Electrical stimulation mapping guides individualized surgical approach in an epilepsy-associated tumor within language representing cortex
- Arts and psychomotor therapies in the treatment of personality disorders
- Arts and psychomotor therapies in the treatment of personality disorders
- Commentary on: A new genetic variant, presenting as young onset rapidly progressive dementia and parkinsonism
- Conjugal Synucleinopathies: A Clinicopathologic Study
- Conjugal Synucleinopathies: A Clinicopathologic Study
- Creutzfeldt-Jakob disease in a man surviving COVID-19: disentangling a casual or causal association by neuropathology
- Pathogenic Potential of Eomesodermin-Expressing T-Helper Cells in Neurodegenerative Diseases
- Cryopyrin-associated periodic fever syndrome (CAPS) presenting as early-onset dementia, lacking typical recurrent fever or skin rash: a case report
- The natural history of progressive myoclonus Ataxia
- Expansion of highly interferon-responsive T cells in early-onset Alzheimer's disease
- Ictal Cotard delusion as a manifestation of nonconvulsive status epilepticus: A case report and commentary
- Myopathy related to chronic Graft-Versus-Host Disease: From clinic to histological & immunological characterization by imaging mass cytometry
- Persistent GDNF Expression 45 Months after Putaminal Infusion of AAV2-GDNF in a Patient with Parkinson's Disease
- Long-term clinical observation of patients with heterozygous KIF1A variants
- Artificial Intelligence/Machine Learning: The New Frontier of Clinical Pharmacology and Precision Medicine
- a-Synuclein seed amplification assay detects Lewy body co-pathology in autosomal dominant Alzheimer's disease late in the disease course and dependent on Lewy pathology burden
- Imagery-Focused Therapy for Visual Hallucinations: A Case Series
- Early-Onset Autosomal Dominant Myopathy with Vacuolated Fibers and Tubular Aggregates but No Periodic Paralysis, in a Patient with the c.1583G>A (p.R528H) mutation in the CACNA1S Gene
- Early-Onset Autosomal Dominant Myopathy with Vacuolated Fibers and Tubular Aggregates but No Periodic Paralysis, in a Patient with the c.1583G>A (p.R528H) mutation in the CACNA1S Gene
- Case report-Depression with psychotic features as an atypical presentation of neurosyphilis
- The interplay of psychosis and non-compliance with fatal outcome in an adult with MSUD
- Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism
- Artificial intelligence in medicine: A primer and recommendation
- Mirtazapine Monotherapy for Antipsychotics-refractory Psychosis in a Patient with Very-late-onset Schizophrenia-like Psychosis: A Case Report
- FKRP-related muscular dystrophy responsive to immunotherapy
- Ethical responses to violence toward health care workers
- Case report: A novel mutation of glial fibrillary acidic protein gene causing juvenile-onset Alexander disease
- Case report: A novel mutation of glial fibrillary acidic protein gene causing juvenile-onset Alexander disease
- Artificial intelligence enabled histological scoring in ulcerative colitis: Are we ready yet?
- The generative artificial intelligence revolution: How hospitalists can lead the transformation of medical education
- Reply to Glycemic Index/Load Effect on ALS Progression: Potential Interaction with Riluzole
- Palliative care and suicidality: Complicated conversations at two ends of the spectrum
- CBMH special issue editorial: Neurodivergent conditions and criminal behaviour
- CBMH special issue editorial: Neurodivergent conditions and criminal behaviour
- Acute alcohol intoxication presenting acquired lesion of the corpus callosum in a young healthy woman: A case of possible Marchiafava-Bignami disease
- Integrating safety and health practices in therapeutic communities: Insights from Taiwan's Chieh-Lo-Shan Villa
- Case of Hallervorden-Spatz Syndrome: A Tale of Twin Sisters
- Prevalence and Diagnostic Journey of Friedreich's Ataxia in the State of São Paulo, Brazil
- Symptomatic progression of frontotemporal dementia with the TARDBP I383V variant
Evidence Blueprint
Correction to “Gerstmann-Straussler-Scheinker Disease Presenting as Late-Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology”
☊ AI-Driven Related Evidence Nodes
(recent articles with at least 5 words in title)
More Evidence
Correction to “Gerstmann-Straussler-Scheinker Disease Presenting as Late-Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology”
🌐 365 Days
AI Virtual Reality Related Evidence Matrix
- Gerstmann-Sträussler-Scheinker Disease Presenting as Late-Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology
- BCL11B-Related Dystonia: Further Evidence of an Emerging Cause of Childhood-Onset Generalized Dystonia
- Aceruloplasminemia: Unique Clinical and MRI Findings in a Patient with a Novel Frameshift Mutation
- Neurophysiological Analysis of Cortical Myoclonic Tremor and Excessive Startle in ARHGEF9 Deficiency
- A Case of NEDMAGA: Neurodevelopmental Disorder with Movement Abnormalities, Abnormal Gait, and Autistic Features
- Tongue Tremor as a Manifestation of Syphilitic Dementia. A Glimpse into the Past
- Fatigue Impacts Quality of Life in People with Spinocerebellar Ataxias
- Parkinson's Disease Associated with G2019S LRRK2 Mutations without Lewy Body Pathology
- Perry Disease: Expanding the Genetic Basis
- Late Presentation of Chronic Traumatic Encephalopathy in a Former Association Football Player
- Autoimmune Movement Disorders Complicating Treatment with Immune Checkpoint Inhibitors
- Understanding Anxiety in Cervical Dystonia: An Imaging Study
- How to Use the New European Academy of Neurology/Movement Disorder Society European Section Guideline for Invasive Therapies in Parkinson's Disease
- Clinical and Pathological Features of FTDP-17 with MAPT p.K298_H299insQ Mutation
- What are the Key Phenomenological Clues to Diagnose Functional Tic-Like Behaviors in the Pandemic Era?
- Brain Bank Questionnaire Helps in Differential Diagnosis of Movement Disorders: An Autopsy Study of 150 Patients
- X-Linked Levodopa-Responsive Parkinsonism-Epilepsy Syndrome: A Novel PGK1 Mutation and Literature Review
- Motor Complications in Parkinson's Disease: Results from 3343 Patients Followed for up to 12 Years
- Are Cognitive Symptoms Part of the Phenotypic Spectrum of Idiopathic Adult-Onset Dystonia? Summary of Evidence from Controlled Studies
- Improving Conversations about Parkinson's Dementia
- Levodopa-Induced Dyskinesias are Frequent and Impact Quality of Life in Parkinson's Disease: A 5-Year Follow-Up Study
- Global Perceptions and Utilization of Clinical Neurophysiology in Movement Disorders
- Family History of AD/Dementia, Polygenic Risk Score for AD, and Parkinson's Disease
- Tau in Atypical Parkinsonisms: A Meta-Analysis of in Vivo PET Imaging Findings
- Assessing the Severity of Cervical Dystonia: Ask the Doctor or Ask the Patient?
- Deep Brain Stimulation for Orthostatic Tremor: An Observational Study
- Stigma and Social Avoidance in Adults with Essential Tremor
- Premonitory Urge and Tic Severity, Comorbidities, and Quality of Life in Chronic Tic Disorders
- Genetic and pathological features encipher the phenotypic heterogeneity of Gerstmann-Sträussler-Scheinker disease
- A New Definition of Psychosis Is Needed in Parkinson's Disease
- Increased Frequency of Self-Reported Obsessive-Compulsive Symptoms in Patients with Functional Movement Disorders
- Confirmation of the Pathogenetic Role of the CCDC88C Gene in Early-Onset Pure Spastic Paraplegia
- Challenges and Future of the International Parkinson and Movement Disorder Society Prodromal Parkinson's Disease Criteria: Are We On the Right Track?
- Non-GAA Repeat Expansions in FGF14 Are Likely Not Pathogenic-Reply to: "Shaking Up Ataxia: FGF14 and RFC1 Repeat Expansions in Affected and Unaffected Members of a Chilean Family"
- Safety and Efficacy of Long-Term Deutetrabenazine Use in Children and Adolescents with Tics Associated with Tourette Syndrome: An Open-Label Extension Study
- Optic Disc and Retinal Architecture Changes in Patients with Spinocerebellar Ataxia Type 2
- Novel PANK2 Variant in Asian Indians with Atypical Pantothenate Kinase Associated Neurodegeneration
- Digital Gait Measures Capture 1-Year Progression in Early-Stage Spinocerebellar Ataxia Type 2
- Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4
- Accuracy of the Early Diagnosis of Parkinson's Disease
- Prevalence and Incidence of Huntington's Disease
- Variability in the Accuracy of Clinical Diagnosis of Early Parkinson's Disease
- Autosomal Dominant MPAN: Mosaicism Expands the Clinical Spectrum to Atypical Late-Onset Phenotypes
- Disease Progression in Multiple System Atrophy: The Value of Clinical Cohorts with Long Follow-Up
- Reply to Letter to the Editor: Prevalence and Incidence of Huntington's Disease Comment on Medina et al. (2022)
- Clinical and imaging predictors of late-onset GM2 gangliosidosis: A scoping review
- Localized Changes in Dentate Nucleus Shape and Magnetic Susceptibility in Friedreich Ataxia
- Correction to "Comparing randomized controlled trials of outpatient family-based or inpatient multimodal treatment followed by outpatient care in youth with anorexia nervosa: Differences in populations, metrics, and outcomes"
- Reply to 'Comment on Martino et al. 'Scales for Antipsychotic-Associated Movement Disorders: Systematic Review, Critique, and Recommendations'"
- Comment on "Summing MDS-UPDRS Parts 1 + 2 (Nonmotor and Motor Experience of Daily Living): The Patient's Voice"
- A life lost to anorexia nervosa: A case report of rapid progressive disease and its psychological aspects
- Primary progressive aphasia with focal periodic sharp wave complexes: An unusual manifestation of Creutzfeldt-Jakob disease
- Neuropsychology of late-onset epilepsies
- Ma2 antibody-associated limbic encephalitis: The early etiology treatment may modify the disease clinical trajectory
- A case for re-conceptualizing the 'atypical'-A lived experience perspective
- Steroid responsive encephalopathy associated with autoimmune thyroiditis (SREAT) presenting as subacute psychosis: Case report and literature review
- Deep Brain Stimulation Improves Parkinson's Disease-Associated Pain by Decreasing Spinal Nociception
- Congenital diaphragmatic hernia in patient with 1p36 deletion
- Novel method for classification of prion diseases by detecting PrPres signal patterns from formalin-fixed paraffin-embedded samples
- Gerstmann Syndrome Case-Control Study: Correlation between Brain Lesions & Functional Disability
- Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and Duration
- Long-Term Nicotinamide Riboside Use Improves Coordination and Eye Movements in Ataxia Telangiectasia
- Impact of Magnetic Resonance Imaging Markers on the Diagnostic Performance of the International Parkinson and Movement Disorder Society Multiple System Atrophy Criteria
- Homozygous deep intronic variant in SNX14 cause autosomal recessive Spinocerebellar ataxia 20: a case report