• "One a penny, two a penny", I saw the hot cross bun sign"
• A Case of Idiopathic Intracranial Hypertension Complicated with both Infratentorial and Supratentorial Cortical Superficial Siderosis: Novel Imaging Findings on Intravoxel Incoherent Motion Magnetic Resonance Imaging Offering Clues to Pathophysiology
• A Case of Prolonged Wernicke's Encephalopathy After Treatment With IV Thiamine Due to the Subsequent Development of Refeeding Syndrome
• A female adult-onset X-ALD patient with pure cerebellar symptoms:a case report
• A homozygous nonsense variant in the alternatively spliced VLDLR exon 4 causes a neurodevelopmental disorder without features of VLDLR cerebellar hypoplasia
• A novel KCND3 variant in the N-terminus impairs the ionic current of Kv4.3 and is associated with SCA19/22
• A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes
• A rare case of acute cerebellitis due to enterovirus treated with therapeutic plasma exchange: Case report and review of the literature
• Acute Cerebellar Manifestations without Limbic Involvement in GABA(B) Receptor Autoimmune Encephalitis: Case Report and Literature Review
• Acute Cerebellitis and Obstructive Hydrocephalus: An Unseen Neurological Complication After Surgical Repair for Tetralogy of Fallot
• An autopsy case of progressive supranuclear palsy with severe corticospinal tract degeneration
• Anatomical and functional analysis of the corticospinal tract in an FRDA mouse model
• Anti-Purkinje Cell Cytoplasmic Antibody Type 2-Associated Autoimmune Cerebellar Degeneration in Children: A Different Phenotype From Adults
• Association study of GBA1 variants with MSA based on comprehensive sequence analysis -Pitfalls in short-read sequence analysis depending on the human reference genome
• Autoimmune Movement Disorders
• Autoimmune Neurobeachin Cerebellar Ataxia
• Bromelain decreases oxidative stress and Neuroinflammation and improves motor function in adult male rats with cerebellar Ataxia induced by 3-acetylpyridine
• Cerebellar ataxia, neuropathy and vestibular areflexia syndrome: a neurogenic cough prototype
• Cerebellar contribution to cognitive deficits and prefrontal cortex dysfunction in Spinocerebellar Ataxia Type 1 (SCA1)
• Cerebellar form of multiple system atrophy: A case report
• Cerebellar nuclei cells produce distinct pathogenic spike signatures in mouse models of ataxia, dystonia, and tremor
• Cerebellitis following COVID-19 infection: A case-based systematic review and pooled analysis
• Clinical and genetic variability among Bulgarian patients with autosomal recessive spastic ataxia of Charlevoix-Saguenay
• Clinical characteristics and outcomes after trigeminal schwannoma resection: a multi-institutional experience
• Clinical utility of square-wave jerks in neurology and psychiatry
• Clinical, genetic, and neuroimaging profiles of autosomal recessive spinocerebellar ataxia type 4 caused by novel VPS13D variants in Chinese
• Comprehensive Evaluation of Sporadic Late-Onset Cerebellar Ataxias: Clinical Presentation, Diagnostic Challenges, and Treatment Outcomes
• Comprehensive Physiotherapy Rehabilitation in a Patient With Cerebellar Ataxia and Dysphagia: A Case Report Investigating Symptomatology, Management, and Outcomes
• COVID-19-Associated Cerebellar Ataxia: A Case Series
• Dentatorubral-pallidoluysian atrophy: a rare cause of epilepsy, ataxia and chorea
• Diagnostic and prognostic biomarkers in immune checkpoint inhibitor-related encephalitis: a retrospective cohort study
• Early-onset dysphagia predicts short survival in multiple system atrophy
• Early-onset palatal myoclonus in Wernekinck commissure syndrome secondary to caudal paramedian midbrain infarction: A case report and a mini review of the literature
• Early-Onset Palatal Myoclonus in Wernekink Commissure Syndrome Secondary to Caudal Paramedian Midbrain Infarction: a Case Report and a Mini Review of the Literature
• Effect of Korean Red Ginseng on the motor performance and ataxia
• Effects of Anodal tDCS Applied Over the Cerebellum Combined with Physical Therapy on Center of Gravity Sway in a Patient with Cerebellar Ataxia: A Single-Case Study
• Exome sequencing confirms the clinical diagnosis of both joubert syndrome and klinefelter syndrome with keratoconus in a han Chinese family
• Expanding the genetic and phenotypic landscape of replication factor C complex-related disorders: RFC4 deficiency is linked to a multisystemic disorder
• Exploring functional and structural connectivity disruptions in spinocerebellar ataxia type 3: Insights from gradient analysis
• Expression analysis of <em>thg1l</em> during <em>Xenopus laevis</em> development
• External Laryngeal Tremor in Adult-Onset Alexander Disease: A Case Report
• Feasibility of whole-body MRI for cancer screening in children and young people with ataxia telangiectasia: A mixed methods cross-sectional study
• Functional evaluation of novel variants of <em>B4GALNT1</em> in a patient with hereditary spastic paraplegia and the general population
• Gait rhythm analysis as a new continuous scale for cerebellar ataxia: Power law and lognormal components represent the ataxic gait quantity
• Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implications
• Genetic profiles of multiple system atrophy revealed by exome sequencing, long-read sequencing and spinocerebellar ataxia repeat expansion analysis
• Glial cell activation precedes neurodegeneration in the cerebellar cortex of the YG8-800 murine model of Friedreich ataxia
• Glioneuronal tumor in an autosomal-dominant polycystic kidney disease patient: a case report and literature review
• Gluten Ataxia and mGluR1 Autoimmune Encephalitis Presenting as Acute Cerebellar Ataxia: A Case Report
• Hematopoietic stem/progenitor cell transplantation recovers immune defects and prevents lymphomas in Atm-deficient mice
• Horizontal Pendular Nystagmus and Ataxia Secondary to Severe Hypomagnesemia
• Hot cross bun sign in JC-Virus Granule cell neuronopathy in HIV infected patient - a case report
• Immune Checkpoint Inhibitor-Related Cerebellar Toxicity: Clinical Features and Comparison with Paraneoplastic Cerebellar Ataxia
• Immune profiling and functional analysis of NK and T cells in ataxia telangiectasia
• Investigation of Spinocerebellar Ataxia (SCA) Disease in Iranian Patients and Accurate Trinucleotide Repeat Detection in the SCA3 by TP-PCR Method
• Lessons from the ATTeST trial in ataxia telangiectasia
• Linking abnormal neural activity patterns to motor deficits
• Live Streaming of the Professor's Ward Rounds in Undergraduate Neurology Education: Usability Study
• Longitudinal Changes of Clinical, Imaging, and Fluid Biomarkers in Preataxic and Early Ataxic Spinocerebellar Ataxia Type 2 and 7 Carriers
• Loss of Elp1 in cerebellar granule cell progenitors models ataxia phenotype of Familial Dysautonomia
• Low prevalence of SCA27B in adult-onset cerebellar ataxia cohort of Jewish ancestry
• Maculopathy and adult-onset ataxia in patients with biallelic MFSD8 variants
• Might patients with cerebellar ataxia benefit from the Computer Assisted Rehabilitation ENvironment (CAREN)? A pilot study focusing on gait and balance
• Minimal Detectable Change of Cough and Lingual Strength Outcomes in Neurodegenerative Disease
• Multimodal, Longitudinal Profiling of SCA1 Identifies Predictors of Disease Severity and Progression
• Mutations in Genes Encoding Subunits of the RNA Exosome as a Potential Novel Cause of Thrombotic Microangiopathy
• Natural history of non-polyglutamine CACNA1A disease in Austria
• Neurodegeneration With Brain Iron Accumulation in a Case of Adult Aceruloplasminemia
• Neurologic Deficits Following Oral Misuse of the Nasal Decongestant Propylhexedrine
• Neurological Complications of COVID-19 Infection: A Comprehensive Review
• Nilotinib treatment outcomes in autosomal dominant spinocerebellar ataxia over one year
• Oculomotor and Vestibular Deficits in Friedreich Ataxia - Systematic Review and Meta-Analysis of Quantitative Measurements
• Opsoclonus-Ataxia Syndrome in a Patient With Small-Cell Lung Cancer Treated With Immune Checkpoint Inhibitors
• Opsoclonus-myoclonus-ataxia syndrome associated with bacterial urinary tract infection
• Oxidative stress and the multifaceted roles of ATM in maintaining cellular redox homeostasis
• Paraneoplastic neurological syndromes of small cell lung cancer
• Paroxysmal movement disorders
• Partial Rhombencephalosynapsis Presenting in an Adult with Cerebello-Trigeminal-Dermal Dysplasia
• Phenotypic Spectrum and Natural History of Gillespie Syndrome. An Updated Literature Review with 2 New Cases
• Phenotypic variability related to dominant UCHL1 mutations: about three families with optic atrophy and ataxia
• Preimplantation Genetic Testing of Spinocerebellar Ataxia Type 3/Machado-Joseph Disease-Robust Tools for Direct and Indirect Detection of the ATXN3 (CAG)(n) Repeat Expansion
• Primary Immunodeficiency-Type Ataxia-Telangiectasia Revealed by Splenic Abscesses
• Production of Spinocerebellar Ataxia Type 3 Model Mice by Intravenous Injection of AAV-PHP.B Vectors
• Progress of ATM inhibitors: Opportunities and challenges
• Recent advances in diagnosis of immune-mediated cerebellar ataxias: novel concepts and fundamental questions on autoimmune mechanisms
• Safety and efficacy of intra-erythrocyte dexamethasone sodium phosphate in children with ataxia telangiectasia (ATTeST): a multicentre, randomised, double-blind, placebo-controlled phase 3 trial
• Sensitivity of Advanced Magnetic Resonance Imaging to Progression over Six Months in Early Spinocerebellar Ataxia
• Somatic instability of the <em>FGF14</em> -SCA27B GAA•TTC repeat reveals a marked expansion bias in the cerebellum
• Specific Biomarkers in Spinocerebellar Ataxia Type 3: A Systematic Review of Their Potential Uses in Disease Staging and Treatment Assessment
• Spinocerebellar Ataxias: Phenotypic Spectrum of PolyQ versus Non-Repeat Expansion Forms
• SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X-Linked Intellectual Disability
• Stiff Person Syndrome and GAD Antibody-Spectrum Disorders
• Streamlined two-step fragment analysis PCR and exome sequencing of RFC1 for diagnostic testing of suspected CANVAS patients
• The cerebellum computes frequency dynamics for motions with numerical precision and cross-individual uniformity
• The episodic ataxias
• The New Face of Dynamic Mutation-The CAA [CAG]n CAA CAG Motif as a Mutable Unit in the TBP Gene Causative for Spino-Cerebellar Ataxia Type 17
• The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy
• Toll-like receptor 4 deficiency in Purkinje neurons drives cerebellar ataxia by impairing the BK channel-mediated after-hyperpolarization and cytosolic calcium homeostasis
• Two patients of immunotherapy-responsive autoimmune cerebellar ataxia fulfilled with criteria of multiple system atrophy
• Whole genome joint analysis reveals ATM:C.1564_1565del variant segregating with Ataxia-Telangiectasia and breast cancer