Disease: Cerebellar ataxia
- <em>ATP1A3</em> Disease Spectrum Includes Paroxysmal Weakness and Encephalopathy Not Triggered by Fever
- 18F-FDG Brain PET/MRI in Chronic Lymphocytic Inflammation With Pontine Perivascular Enhancement Responsive to Steroids
- A 52-Year-Old Woman With Dysarthria, Ataxia, Xanthelasmas, and Miliary Pulmonary Nodules
- A case of Holmes tremor in which <sup>123</sup>I-IMP SPECT and MRI findings suggest damage to the cerebellothalamic tract and the dentato-rubro-olivary pathway
- A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy
- AAV-Mediated CAG-Targeting Selectively Reduces Polyglutamine-Expanded Protein and Attenuates Disease Phenotypes in a Spinocerebellar Ataxia Mouse Model
- Application of bedside HINTS, ABCD(2) score and truncal ataxia to differentiate cerebellar-brainstem stroke from vestibular neuritis in the emergency room
- Ataxia telangiectasia and Rad3-related (ATR) inhibition by VE-822 potently reversed 5-flourouracil resistance in colorectal cancer cells through targeting DNA damage response
- Ataxia telangiectasia: a rare case report from Nepal
- Autoimmune nodopathy with anti-contactin 1 antibody characterized by cerebellar dysarthria: a case report and literature review
- Autosomal recessive spinocerebellar ataxia type 4 due to a novel homozygous mutation in the VPS13D gene in a Saudi family
- Bilateral vestibulopathy as the initial presentation of CANVAS
- Brain Volumes in Opsoclonus-Myoclonus Ataxia Syndrome: A Longitudinal Study
- Capecitabine-Related Fourth Nerve Palsy: A Case Report
- Case Presentation of Autoimmune Septin-5 Cerebellar Ataxia
- Case report: Novel NUS1 variant in a Chinese patient with tremors and intellectual disability
- Central nervous system adverse events of immune checkpoint inhibitors
- Cerebellar blood perfusion is a diagnostic, but not a prognostic, marker for parkinsonian-dominant type multiple system atrophy
- Cerebellar degeneration in gluten ataxia is linked to microglial activation
- Clinical and Genetic Characterization of a Cohort of Brazilian Patients With Congenital Ataxia
- Clinical and genetic spectrum of 6 cases with asparagine synthetase deficiency
- Clinical and Imaging Profile of Patients with Cerebrotendinous Xanthomatosis - a Video Case Series from India
- Clinical and Molecular Spectrum of Autosomal Recessive CA8-Related Cerebellar Ataxia
- Clinical Presentation, Management, and Diagnostic Performance of 2021 Criteria for Paraneoplastic Neurologic Syndromes in Childhood
- Cognitive dysfunction, social behavior disorder, cerebellar ataxia, and atypical brain FDG-PET presentation in spinocerebellar ataxia 17: a case report
- Cognitive Impairment Is Part of the Phenotype of Cerebellar Ataxia, Neuropathy, Vestibular Areflexia Syndrome (CANVAS)
- Correction to: Cognitive dysfunction, social behavior disorder, cerebellar ataxia, and atypical brain FDG-PET presentation in spinocerebellar ataxia 17: a case report
- Corrigendum: Remote assessment of cognition in Parkinson's disease and cerebellar ataxia: the MoCA test in English and Hebrew
- CRE24-051: Rare Case of a Paraneoplastic Cerebellar Ataxia Secondary to a Retroperitoneal Neuroendocrine Tumor of Unknown Origin
- Cross-Sectional Analysis of Exome Sequencing Diagnosis in Patients With Neurologic Phenotypes Facing Barriers to Clinical Testing
- Distal oesophageal spasm in a patient with multiple system atrophy: A case report
- DNA Damage-driven Inflammatory Cytokines: Reprogramming of Tumor Immune Microenvironment and Application of Oncotherapy
- DNA-PK and ATM drive phosphorylation signatures that antagonistically regulate cytokine responses to herpesvirus infection or DNA damage
- Dynamic molecular network analysis of iPSC-Purkinje cells differentiation delineates roles of ISG15 in SCA1 at the earliest stage
- Effect of a Home-Base Core Stability Exercises in Hereditary Ataxia. A Randomized Controlled Trial. A Pilot Randomized Controlled Trial
- Effect of Regional Brain Activity Following Repeat Transcranial Magnetic Stimulation in SCA3: A Secondary Analysis of a Randomized Clinical Trial
- Effects of cognitive-motor intervention for pediatric posterior fossa tumor survivors: results of a pilot study
- Efficacy and safety of N-acetyl-L-leucine in patients with ataxia telangiectasia: A randomized, double-blind, placebo-controlled, crossover clinical trial
- Frataxin deficiency shifts metabolism to promote reactive microglia via glucose catabolism
- GAA-FGF14 disease: defining its frequency, molecular basis, and 4-aminopyridine response in a large downbeat nystagmus cohort
- Genetic evidence for splicing-dependent structural and functional plasticity in CASK protein
- Granuloprival cerebellar cortical degeneration in a Yorkshire Terrier and Lagotto Romagnolo dog
- Hungarian adaptation of the cerebellar cognitive affective/Schmahmann Syndrome Scale
- Identification of DAGLA as an autoantibody target in cerebellar ataxia
- Immune Ataxias: The Continuum of Latent Ataxia, Primary Ataxia and Clinical Ataxia
- Inflammatory progressive multifocal leukoencephalopathy with human T-cell lymphotropic virus-1 coinfection
- Informal gold miners with mercury toxicity: Novel asymmetrical neurological presentations
- Integration of graph network with kernel SVM and logistic regression for identification of biomarkers in SCA12 and its diagnosis
- Interest of rare autoantibodies in autoimmune encephalitis and paraneoplastic neurological syndromes: the utility (or futility) of rare antibody discovery
- Joubert syndrome-derived induced pluripotent stem cells show altered neuronal differentiation in vitro
- Lumbar Subarachnoid-Peritoneal Shunting Deteriorates Superficial Siderosis Associated with a Dural Defect
- Memantine suppresses the excitotoxicity but fails to rescue the ataxic phenotype in SCA1 model mice
- Molecular Imaging in CANVAS: A Contribution for Differential Diagnosis?
- Moving across disorders: A cross-sectional study of cognition in early onset ataxia and dystonia
- MRl and MRS hints for the differentiation of cerebellar multiple system atrophy from spinocerebellar ataxia type II
- Multiple system atrophy: an update and emerging directions of biomarkers and clinical trials
- Neuronal antibodies in nonparaneoplastic autoimmune cerebellar ataxias
- Opalski Syndrome and Elucidation of Lateral Medullary Syndrome
- Paraneoplastic cerebellar and brainstem disorders
- Paraneoplastic movement disorders
- Paraneoplastic neurologic syndrome associated with gynecologic and breast malignancies
- Paraneoplastic Syndrome Case Presented As Nystagmus and Ataxia
- Phenotypic analysis of ataxia in spinocerebellar ataxia type 6 mice using DeepLabCut
- Phenotypical, genotypical and pathological characterization of the moonwalker mouse, a model of ataxia
- Posterior Interhemispheric-Transtentorial Approach for Resection of an Arteriovenous Malformation of the Superior Medullary Velum and Fourth Ventricle: 2-Dimensional Operative Video
- Potential Prodromal Digital Postural Sway Markers for Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) Detected via Dual-Tasking and Sensory Manipulation
- Prediction of Individual Disease Progression Including Parameter Uncertainty in Rare Neurodegenerative Diseases: The Example of Autosomal-Recessive Spastic Ataxia Charlevoix Saguenay (ARSACS)
- Preliminary Report of Fully Endoscopic Microvascular Decompression
- Primary central nervous system lymphoma presenting as a unilateral internal auditory canal lesion: a case report
- Primary Coenzyme Q10 Deficiency-4 Causing Young Onset Ataxia-Dystonia
- Primary Coenzyme Q10 Deficiency-Related Ataxias
- Proceedings of the first global meeting of the Posterior Fossa Society: state of the art in cerebellar mutism syndrome
- Progressive ataxia and palatal tremor
- Progressive ataxia and palatal tremor (PAPT) with hypertrophic olivary degeneration (HOD): A case report
- Purkinje cell dysfunction causes disrupted sleep in ataxic mice
- Real-time field-programmable gate array-based closed-loop deep brain stimulation platform targeting cerebellar circuitry rescues motor deficits in a mouse model of cerebellar ataxia
- Research Progress in the Roles of MRE11-RAD50-NBS1 Complex and Human Diseases
- Resection of the quadrangular lobule of the cerebellum to increase exposure of the cerebellomesencephalic fissure: an anatomical study with clinical correlation
- RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia
- RFC1 Repeat Distribution in the Cypriot Population: Study of a Large Cohort of Patients With Undiagnosed Ataxia and Non-Disease Controls
- Scrub typhus with opsoclonus-myoclonus-ataxia-seizure as primary presentations
- Single-Session Cerebellar Transcranial Direct Current Stimulation Improves Postural Stability and Reduces Ataxia Symptoms in Spinocerebellar Ataxia
- Spectrum of <em>ERCC6</em>-Related Cockayne Syndrome (Type B): From Mild to Severe Forms
- Spinocerebellar ataxia 27B (SCA27B), a frequent late-onset cerebellar ataxia
- Spinocerebellar Ataxia Type 3 Pathophysiology-Implications for Translational Research and Clinical Studies
- Teaching Video NeuroImage: Adaptor-Related Protein-Complex-3 Subunit beta-2 Immunoglobulin-G-Associated Autoimmune Ataxia
- The cerebellum acts as the analog to the medial temporal lobe for sensorimotor memory
- The deubiquitinase function of ataxin-3 and its role in the pathogenesis of Machado-Joseph disease and other diseases
- The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population
- The genetic landscape and phenotypic spectrum of GAA-FGF14 ataxia in China: a large cohort study
- The pharmacokinetics and pharmacodynamics of ibogaine in opioid use disorder patients
- The Role of Verbal Fluency in the Cerebellar Cognitive Affective Syndrome Scale in Friedreich Ataxia
- Therapeutic Options Targeting the Ataxia-Telangiectasia Mutated (ATM)-mediated DNA Damage Response, Macropinocytosis, and Adaptive Immunity in Ovarian Cancer
- Transcerebellar ventriculoperitoneal shunt for management of presumed arachnoid diverticulum in the fourth ventricle of a dog
- Transcranial Sonography Characteristics of Cerebellar Neurodegenerative Ataxias
- Two case reports of a novel missense mutation in the PNPLA6 gene in two siblings with chorioretinal dystrophy, hypogonadotropic hypogonadism, and cerebellar ataxia
- Two more families supporting the existence of monogenic spinocerebellar ataxia 48
- Ultra-high-field 7-Tesla magnetic resonance imaging in fragile X tremor/ataxia syndrome (FXTAS)
- Ultrasound-guided resection of cerebellar racemose neurocysticercosis: novel insights from a unique scenario
- Unraveling the molecular landscape of Ataxia Telangiectasia: Insights into Neuroinflammation, immune dysfunction, and potential therapeutic target