• <em>Alchornea laxiflora</em> (Benth.) Pax &amp; K. Hoffman extract protects against lead-induced neurodegeneration in cockerel chickens
• "One a penny, two a penny", I saw the hot cross bun sign"
• 18F-FDG PET/CT in assessment of paraneoplastic cerebellar degeneration as the first sign of occult fallopian tube serous cystadenocarcinoma: Case report
• A novel insight into the neuroprotective effects of cannabidiol: maintained apelin/dopamine synthesis, NRF2 signaling, and AKT/CREB/BDNF gene expressions
• Abundant transcriptomic alterations in the human cerebellum of patients with a C9orf72 repeat expansion
• Altered lipid homeostasis is associated with cerebellar neurodegeneration in SNX14 deficiency
• Ameliorative effects of gallic acid on tebuconazole-induced adverse effects in the cerebellum of adult albino rats: histopathological and immunohistochemical evidence
• An autopsy case of progressive supranuclear palsy with severe corticospinal tract degeneration
• An overview of early-onset cerebellar ataxia: a practical guideline
• Analysis of diffusion changes in cerebral tissues of Parki̇nson's patients who underwent subthalamic nucleus deep brain stimulation: Correlation of improvements in motor and neuropsychiatric symptoms
• 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
• Anti-yo-antibody mediated paraneoplastic cerebellar degeneration - a case series
• Astrovirus induced nonpurulent encephalomyelitis in sheep: First report from Türkiye by high-throughput sequencing
• Basal parasympathetic deficits in C9orf72 hexanucleotide repeat expansion carriers relate to smaller frontoinsula and thalamus volume and lower empathy
• Brain MRI Volumetric Assessment of Patients With Multiple Sclerosis: The Volume of Basal Ganglia, Thalamus, and Posterior Fossa
• Bromelain decreases oxidative stress and Neuroinflammation and improves motor function in adult male rats with cerebellar Ataxia induced by 3-acetylpyridine
• Causal relationship between multiparameter brain MRI phenotypes and age: evidence from Mendelian randomization
• Cerebellar and Olfactory Bulb Perturbations Induced by Vanadium Neurotoxicity in the African Giant Rat (Cricetomys gambianus, Waterhouse)
• Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS): from clinical diagnosis towards genetic testing
• Cerebellar cognitive affective syndrome caused by cerebellar atrophy associated with Wallerian degeneration after pontine haemorrhage: a case report
• Cerebellar contribution to cognitive deficits and prefrontal cortex dysfunction in Spinocerebellar Ataxia Type 1 (SCA1)
• Cerebellar degeneration in gluten ataxia is linked to microglial activation
• Cerebellum Purkinje cell vulnerability in aged rats with memory impairment
• Characterization of monoamine oxidase-B (MAO-B) as a biomarker of reactive astrogliosis in Alzheimer's disease and related dementias
• CircRNA CDR1as affects functional repair after spinal cord injury and regulates fibrosis through the SMAD pathway
• Clinical, imaging and histopathological characterization of a series of three cats with cerebellar cortical degeneration
• Deep Learning-based Approach for Brainstem and Ventricular MR Planimetry: Application in Patients with Progressive Supranuclear Palsy
• Differing patterns of cortical grey matter pathology identified by multifractal analysis in UMN-predominant ALS patients with and without corticospinal tract hyperintensity
• Discovery of a de novo ITPR1 missense mutation in a patient with early-onset cerebellar ataxia: A rare case report of spinocerebellar ataxia 29
• Disrupted cerebellar structural connectome in spinocerebellar ataxia type 3 and its association with transcriptional profiles
• Distinct Longitudinal Brain White Matter Microstructure Changes and Associated Polygenic Risk of Common Psychiatric Disorders and Alzheimer's Disease in the UK Biobank
• 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
• Elevated NLRP3 Inflammasome Activation Is Associated with Motor Neuron Degeneration in ALS
• Endoplasmic reticulum associated degradation preserves neurons viability by maintaining endoplasmic reticulum homeostasis
• Epidemiology of paraneoplastic neurologic syndromes
• Evaluation of histological and ultrastructural changes provoked by prenatal tramadol on postnatal cortical cerebellar neuronal development in rats: possible implication of Ki67, GFAP and MicroRNA-7/P53 signalling trajectories
• Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study
• Exploiting fly models to investigate rare human neurological disorders
• Gait rhythm analysis as a new continuous scale for cerebellar ataxia: Power law and lognormal components represent the ataxic gait quantity
• Gene editing as a therapeutic strategy for spinocerebellar ataxia type-3
• Generation and characterization of cerebellar granule neurons specific knockout mice of Golli-MBP
• Genetic evidence for splicing-dependent structural and functional plasticity in CASK protein
• Glial cell activation precedes neurodegeneration in the cerebellar cortex of the YG8-800 murine model of Friedreich ataxia
• Gradient of microstructural damage along the dentato-thalamo-cortical tract in Friedreich ataxia
• Granuloprival cerebellar cortical degeneration in a Yorkshire Terrier and Lagotto Romagnolo dog
• Gynecologic clear cell carcinoma and paraneoplastic cerebellar Degeneration: A literature review and case study
• Harlequin mice exhibit cognitive impairment, severe loss of Purkinje cells and a compromised bioenergetic status due to the absence of Apoptosis Inducing Factor
• Hematologic malignancies and hematopoietic stem cell transplantation
• Hypertrophic olivary degeneration secondary to a Guillain Mollaret triangle cavernoma: Two case report
• Hypertrophy of the inferior olivary nucleus in corticobasal degeneration: A neuropathological study
• Immune Ataxias: The Continuum of Latent Ataxia, Primary Ataxia and Clinical Ataxia
• Impact of Magnetic Resonance Imaging Markers on the Diagnostic Performance of the International Parkinson and Movement Disorder Society Multiple System Atrophy Criteria
• Incidence and Characteristics of Cerebellar Atrophy/Volume Loss in Children with Confirmed Diagnosis of Tuberous Sclerosis Complex
• KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing
• Long-Term Follow-Up before and during Riluzole Treatment in Six Patients from Two Families with Spinocerebellar Ataxia Type 7
• Maculopathy and adult-onset ataxia in patients with biallelic MFSD8 variants
• Magnetic resonance imaging pattern recognition of metabolic and neurodegenerative encephalopathies in dogs and cats
• Multi-omics profiling reveals dysregulated ribosome biogenesis and impaired cell proliferation following knockout of CDR2L
• Multiscale brain age prediction reveals region-specific accelerated brain aging in Parkinson's disease
• Neuroglobin overexpression in cerebellar neurons of Harlequin mice improves mitochondrial homeostasis and reduces ataxic behavior
• Neuroimaging and clinical features of bilateral Wallerian degeneration of middle cerebellar peduncles subsequent to pontine infarction
• No Evidence for Semantic Prediction Deficits in Individuals With Cerebellar Degeneration
• Overview of treatment strategies in paraneoplastic neurological syndromes
• Paraneoplastic cerebellar and brainstem disorders
• Paraneoplastic Cerebellar Degeneration Revealing Non-Small Cell Lung Cancer: A Case Report
• Paraneoplastic neurologic syndrome associated with gynecologic and breast malignancies
• Paraneoplastic neurological syndromes of small cell lung cancer
• Paraneoplastic syndromes in patients with melanoma
• Pathogenesis and immunopathology of paraneoplastic disorders
• Phenotypical, genotypical and pathological characterization of the moonwalker mouse, a model of ataxia
• Prepubertal Repeated Berberine Supplementation Enhances Cerebrocerebellar Functions by Modulating Neurochemical and Behavioural Changes in Wistar Rats
• Preserved VPS13A distribution and expression in Huntington's disease: divergent mechanisms of action for similar movement disorders?
• Progress of ATM inhibitors: Opportunities and challenges
• Progressive ataxia and palatal tremor (PAPT) with hypertrophic olivary degeneration (HOD): A case report
• Progressive Cerebrocerebellar Uncoupling in Sporadic and Genetic Forms of Amyotrophic Lateral Sclerosis
• Progressive Supranuclear Palsy Diagnosed After a Severe Fall Trauma in a Patient Who Experienced Episodes of Easy Falling
• Recent advances in diagnosis of immune-mediated cerebellar ataxias: novel concepts and fundamental questions on autoimmune mechanisms
• Resveratrol and 1,25-dihydroxyvitamin D decrease Lingo-1 levels, and improve behavior in harmaline-induced Essential tremor, suggesting potential therapeutic benefits
• Role of the Cerebellum in Bipolar Disorder: A Systematic Literature Review
• Role of the globus pallidus in motor and non-motor symptoms of Parkinson's disease
• Sensorimotor Integration in Patients with Voice Disorders: A Scoping Review of Behavioral Research
• Sensorineural correlates of failed functional recovery after natural regeneration of vestibular hair cells in adult mice
• Significant improvement in paraneoplastic neurological syndromes without identifiable anti-neural antibodies in patients with breast cancer after breast surgery
• Spinocerebellar ataxia 27B (SCA27B), a frequent late-onset cerebellar ataxia
• Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia-experience from an Italian cohort
• Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs
• Spinocerebellar Ataxias: Phenotypic Spectrum of PolyQ versus Non-Repeat Expansion Forms
• Spliceosomal GTPase Eftud2 deficiency-triggered ferroptosis leads to Purkinje cell degeneration
• Subacute combined degeneration of the spinal cord with cerebellar lesions: A case report
• The artifact of cerebellar granule cell layer conglutination in veterinary medicine: a brief historical perspective and review
• The cerebellum acts as the analog to the medial temporal lobe for sensorimotor memory
• The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population
• 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
• Triggered saccadic oscillations: case series and review of the literature
• Two-Month Voluntary Ethanol Consumption Promotes Mild Neuroinflammation in the Cerebellum but Not in the Prefrontal Cortex, Hippocampus, or Striatum of Mice
• Unraveling the molecular landscape of Ataxia Telangiectasia: Insights into Neuroinflammation, immune dysfunction, and potential therapeutic target
• Vestibular Rehabilitation of Patient with Hypertrophic Olivary Degeneration: A Case Report
• Zonisamide Ameliorated the Apoptosis and Inflammation in Cerebellar Tissue of Induced Alcohol Addiction Animal Model