Disease: Chorea minor
- A 78-Year-Old Woman with Sudden Onset of Left-Sided Hemiballismus
- A Case of Chorea with Slow Saccades Caused by NKX2-1 Mutation
- A case of immunotherapy-responsive autoimmune hemichorea
- A case presentation of paroxysmal hypnogenic dyskinesia: clinical features and management
- A case report of a patient with neurodevelopmental disorder with impaired speech and hyperkinetic movements: A biallelic variant in the ZNF142 gene
- Activation of alpha-7 nicotinic acetylcholine receptor by tropisetron mitigates 3-nitropropionic acid-induced Huntington's disease in rats: Role of PI3K/Akt and JAK2/NF-κB signaling pathways
- Acute Hemichorea in an Elderly Patient With Positive Anti-centromere Antibodies and Lung Tumor
- Adult-onset acute rheumatic fever with chorea and carditis
- Alterations in Cerebrospinal Fluid Urea Occur in Late Manifest Huntington's Disease
- An exploration of the genetics of the mutant Huntingtin (mHtt) gene in a cohort of patients with chorea from different ethnic groups in sub-Saharan Africa
- Analysis and validation of potential ICD-related biomarkers in development of myopia using machine learning
- Analysis of characteristics of movement disorders in patients with anti-N-methyl-D-aspartate receptor encephalitis
- Assessment of Perivascular Space Morphometry Across the White Matter in Huntington's Disease Using MRI
- Assessment of Postural Control in Children with Movement Disorders by Means of a New Technological Tool: A Pilot Study
- Attenuated huntingtin gene CAG nucleotide repeat size in individuals with Lynch syndrome
- BDNF and TRiC-inspired reagent rescue cortical synaptic deficits in a mouse model of Huntington's disease
- Before Hemichorea Can Be Attributed to Diabetic Striatopathy, All Other Causes Must Be Thoroughly Ruled Out
- Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome
- Case report: Treatment of Wilson's disease by human amniotic fluid administration
- Ceftriaxone-Induced Encephalopathy in a Patient With Chronic Kidney Disease
- Cerebrospinal fluid glial fibrillary acidic protein, in contrast to amyloid beta protein, is associated with disease symptoms in Huntington's disease
- Characterizing Heart Rate Variability Response to Maximal Exercise Testing in People with Huntington's Disease
- Childhood-onset Huntignton´s disease. A rare presentation
- Chorea as the only presenting clinical feature of rheumatic fever: a case report
- Circulating immunome fingerprint in eosinophilic esophagitis is associated with clinical response to proton pump inhibitor treatment
- Clinical Spectrum, Treatment and Outcome of Children with Autoimmune Encephalitis
- Concern about Tominersen in Patients with Huntington's Disease
- Concern about Tominersen in Patients with Huntington's Disease. Reply
- Continuing the search for fluid biomarkers to enhance Huntington's disease staging and therapeutic response
- Copper enhances aggregational toxicity of mutant huntingtin in a Drosophila model of Huntington's Disease
- COVID-19 vaccine related movement disorders: a systematic review
- Dancing Out of Step: A Case of Tuberculous Meningitis Presenting as Childhood Chorea
- Dancing, Lurching and Swaying: An Indian Case of Dentatorubral-Pallidoluysian Atrophy
- Deregulated Transcriptome as a Platform for Adrenal Huntington's Disease-Related Pathology
- Diabetic striatopathy in an adult with ketotic hyperglycaemia
- Dietary fasting and time-restricted eating in Huntington's disease: therapeutic potential and underlying mechanisms
- Disentangling the neurobiological bases of temporal impulsivity in Huntington's disease
- Effects of an Angiotensin IV Analog on 3-Nitropropionic Acid-Induced Huntington's Disease-Like Symptoms in Rats
- Electroconvulsive Therapy for Obsessive and Compulsive Symptoms in Preclinical Huntington Disease: A Case Report
- Elevated SLC7A2 expression is associated with an abnormal neuroinflammatory response and nitrosative stress in Huntington's disease
- Elucidating the Impact of Deleterious Mutations on IGHG1 and Their Association with Huntington's Disease
- External evaluation of a deep learning-based approach for automated brain volumetry in patients with huntington's disease
- Freesurfer Software Update Significantly Impacts Striatal Volumes in the Huntington's Disease Young Adult Study and Will Influence HD-ISS Staging
- Further learning of clinical characteristics and imaging manifestations of nonketotic hyperglycemic hemichorea
- Gait instability, ophthalmoplegia, and chorea with orofacial dyskinesia in a man with anti-Ri antibodies: a case report
- Genetic testing for non-parkinsonian movement disorders: Navigating the diagnostic maze
- Genome-wide screening identifies Trim33 as an essential regulator of dendritic cell differentiation
- Globus Pallidus Lesion With Iron Deposition and Dopaminergic Denervation in a Patient With a Pathogenic <em>SLC6A1</em> Variant: A Case Report
- Glycine transporter-1 inhibition by NFPS promotes neuroprotection against striatal damage models
- Health state utility estimates for value assessments of novel treatments in Huntington's disease: a systematic literature review
- Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissues
- Huntington's Disease Clinical Trials Corner: March 2024
- Huntington's Disease: A Report of an Interesting Case and Literature Review
- Huntington's Disease: Complex Pathogenesis and Therapeutic Strategies
- Hyperglycemia-induced hemichorea-hemiballismus syndrome - a systematic review
- I<sup>123</sup>-FP-CIT (DaTSCAN) SPECT beyond the Most Common Causes of Parkinsonism: A Systematic Review
- Identification of four novel mutations in VSP13A in Iranian patients with Chorea-acanthocytosis (ChAc)
- Identifying and verifying Huntington's disease subtypes: Clinical features, neuroimaging, and cytokine changes
- Imaging and Assay of the Dynamics of Cytotoxic Huntingtin (HTT) Protein Aggregates Regulated by lncRNAs
- Innovative prognostic modeling in ESCC: leveraging scRNA-seq and bulk-RNA for dendritic cell heterogeneity analysis
- Intravenous MSC-Treatment Improves Impaired Brain Functions in the R6/2 Mouse Model of Huntington's Disease via Recovered Hepatic Pathological Changes
- Language-Independent Acoustic Biomarkers for Quantifying Speech Impairment in Huntington's Disease
- Large animal models for Huntington's disease research
- Longitudinal alterations in brain perfusion and vascular reactivity in the zQ175DN mouse model of Huntington's disease
- Mono- and Biallelic Inactivation of Huntingtin Gene in Patient-Specific Induced Pluripotent Stem Cells Reveal HTT Roles in Striatal Development and Neuronal Functions
- Movement disorders associated with pediatric encephalitis
- Mutant huntingtin protein induces MLH1 degradation, DNA hyperexcision, and cGAS-STING-dependent apoptosis
- Neuroimaging-guided diagnosis of possible FTLD-FUS pathology: a case report
- Nonketotic hyperglycemia hemichorea and hemiballismus: a case report
- Opposing Motor Memories in the Direct and Indirect Pathways of the Basal Ganglia
- Orphan GPR52 as an emerging neurotherapeutic target
- Paraneoplastic movement disorders
- Patient-derived neuron model: Capturing age-dependent adult-onset degenerative pathology in Huntington's disease
- PDE10A Mutation as an Emerging Cause of Childhood-Onset Hyperkinetic Movement Disorders: A Review of All Published Cases
- Postmortem neuropathology in early Huntington disease
- Posttranscriptional regulation of <em>FAN1</em> by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington's disease
- Primary catastrophic antiphospholipid syndrome in children with midbrain infarction: a case report
- Progressive alterations in polysomal architecture and activation of ribosome stalling relief factors in a mouse model of Huntington's disease
- Repetitive Transcranial Magnetic Stimulation for Major Depressive Disorder in Huntington Disease Patient with Improvement in Neuropsychiatric and Movement Symptoms: A Case Report
- Reply to: "Heterogeneous Phenotypic Evolution in ANO3-Related Dystonia Due to the Recurrent p.Glu510Lys Variant"
- Revealing Non-ketotic Hyperglycemia as a Trigger for Hemichorea-Hemiballismus in Uncontrolled Diabetic Asthmatics: A Case Report
- Ribosome Profiling and Mass Spectrometry Reveal Widespread Mitochondrial Translation Defects in a Striatal Cell Model of Huntington Disease
- Role of autophagy and proteostasis in neurodegenerative diseases: Exploring the therapeutic interventions
- Safety of Deutetrabenazine for the Treatment of Tardive Dyskinesia and Chorea Associated with Huntington Disease
- Solid-state nuclear magnetic resonance in the structural study of polyglutamine aggregation
- Somatic CAG Repeat Stability in a Transgenic Sheep Model of Huntington's Disease
- Splice modulators target PMS1 to reduce somatic expansion of the Huntington's disease-associated CAG repeat
- Structural mechanisms for VMAT2 inhibition by tetrabenazine
- Tardive Dyskinesia With Chorea-Ballism Improved by Valbenazine: A Case Report
- The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency
- The First Case of Huntington's Disease like 2 in Mali, West Africa
- The first Indian patient with benign hereditary chorea due to a de novo mutation in the NKX2-1 gene
- The microbiota-gut-brain axis in Huntington's disease: pathogenic mechanisms and therapeutic targets
- The polyglutamine domain is the primary driver of seeding in huntingtin aggregation
- The potential roles of salivary biomarkers in neurodegenerative diseases
- The value of re-evaluation and thorough family history taking for the diagnostic work-up of chorea
- Theory of Mind in Huntington's Disease: A Systematic Review of 20 Years of Research
- Treatments and Outcomes Among Patients with Sydenham Chorea: A Meta-Analysis
- TYROBP/DAP12 knockout in Huntington's disease Q175 mice cell-autonomously decreases microglial expression of disease-associated genes and non-cell-autonomously mitigates astrogliosis and motor deterioration
- Understanding of referential dependencies in Huntington's disease