• 18F-FDG PET/CT in early phase of sporadic Creutzfeldt-Jacob disease: A case report
• A case of a cerebellar form of progressive multifocal leukoencephalopathy in a patient undergoing peritoneal dialysis
• A Case of Prolonged Wernicke's Encephalopathy After Treatment With IV Thiamine Due to the Subsequent Development of Refeeding Syndrome
• A case report of neonatal incontinentia pigmenti complicated by severe cerebrovascular lesions in one of the male monozygotic twins
• A frameshift mutation in the murine Prkra gene causes dystonia and exhibits abnormal cerebellar development and reduced eIF2alpha phosphorylation
• Abnormal Insula Network Characteristics in Panic Disorder
• Acute Cerebellar Manifestations without Limbic Involvement in GABA(B) Receptor Autoimmune Encephalitis: Case Report and Literature Review
• Alcohol Toxicity in the Developing Cerebellum
• Altered functional connectivity of the default mode network in non-arteritic anterior ischaemic optic neuropathy
• An infected intradural dermoid cyst associated with a complete dermal sinus of the posterior cranial fossa: A case report and literature review
• Anatomical and functional analysis of the corticospinal tract in an FRDA mouse model
• Anatomical Variations to the Vertebral Artery and Posterior Inferior Cerebellar Artery are Associated with the Partial Persistence of Primitive Lateral Basirovertebral Anastomosis
• Brain activations during execution and observation of visually guided sequential manual movements in autism and in typical development: A study protocol
• Brain alterations in Cocaine Use Disorder: Does the route of use matter and does it relate to the treatment outcome?
• Brain and the whole-body bone imaging appearances in Menkes disease: a case report and literature review
• Brain structural and functional abnormalities associated with acute post-traumatic headache: iron deposition and functional connectivity
• Case 331
• Central Positional Nystagmus Can Be the Sole Presentation of Cerebellar Nodulus Infarction
• CEP41, a ciliopathy-linked centrosomal protein, regulates microtubule assembly and cell proliferation
• Cerebellar Roles in Motor and Social Functions and Implications for ASD
• Cerebellar white and gray matter abnormalities in temporal lobe epilepsy: a voxel-based morphometry study
• Combined Chiari Malformation Type I and Syringohydromyelia in a Patient With Intractable Headache
• Comparision of spontaneous brain activity between hippocampal sclerosis and MRI-negative temporal lobe epilepsy
• Complex neural tube and skeletal malformations, resembling Chiari malformations, in two calves
• Compound Heterozygous WARS2 Variants Including a Hypomorphic Allele Cause a Milder Phenotype of Complex Dopa Responsive Dystonia: Case Report and Review of the Literature
• Comprehensive Evaluation of Sporadic Late-Onset Cerebellar Ataxias: Clinical Presentation, Diagnostic Challenges, and Treatment Outcomes
• Congenital syndromic Chiari-like malformation (CSCM) in Holstein cattle: towards unravelling of possible genetic causes
• COVID-19 is associated with changes in brain function and structure: A multimodal meta-analysis of neuroimaging studies
• Cytomegalovirus infection lengthens the cell cycle of granule cell precursors during postnatal cerebellar development
• De novo monoallelic Reelin missense variants act in a dominant-negative manner causing neuronal migration disorders
• De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanism
• Decreased gray matter volume in the anterior cerebellar of attention deficit/hyperactivity disorder comorbid oppositional defiant disorder children with associated cerebellar-cerebral hyperconnectivity: insights from a combined structural MRI and resting-
• Degree centrality-based resting-state functional magnetic resonance imaging explores central mechanisms in lumbar disc herniation patients with chronic low back pain
• Desorption Electrospray Ionization Mass Spectrometry Imaging Techniques Depict a Reprogramming of Energy and Purine Metabolism in the Core Brain Regions of Chronic Social Defeat Stress Mice
• Developing Topics
• Diagnostic value of structural, functional and effective connectivity in bipolar disorder
• Differences in gray matter atrophy and functional connectivity between motor subtypes of Parkinson's disease
• Effects of cognitive behavioural therapy and exposure-response prevention on brain activation in obsessive-compulsive disorder patients: systematic review and meta-analysis
• Establishing and Comparing the Normal apparent Diffusion Coefficient Values of Fetal Organs and Placenta Using 1.5 Tesla and 3.0 T MRI at Various Gestational Age
• Exome sequencing confirms the clinical diagnosis of both joubert syndrome and klinefelter syndrome with keratoconus in a han Chinese family
• Expanding the phenotypic spectrum of MPDZ gene variants: A case report with prenatally detected Dandy-Walker malformation and single ventricle heart
• Expanding the Phenotypic Spectrum of Pathogenic <em>KIAA0586</em> Variants: From Joubert Syndrome to Hydrolethalus Syndrome
• First-trimester 3D fetal neurosonography: five standardised views
• Functional connectivity of the auditory cortex in women with trauma-related disorders who hear voices
• Futile recanalization in patients with basilar artery occlusion: assessment of the underlying etiology and the role of perfusion imaging
• Gradient of microstructural damage along the dentato-thalamo-cortical tract in Friedreich ataxia
• Gray Matters: ViT-GAN Framework for Identifying Schizophrenia Biomarkers Linking Structural MRI and Functional Connectivity
• Gray matters: ViT-GAN framework for identifying schizophrenia biomarkers linking structural MRI and functional network connectivity
• Human organoid model of pontocerebellar hypoplasia 2a recapitulates brain region-specific size differences
• Identification of schizophrenia by applying interpretable radiomics modeling with structural magnetic resonance imaging of the cerebellum
• Identification of TCTN1 gene variants in a fetus with Joubert syndrome 13
• Imaging findings and MRI patterns in a cohort of 18q chromosomal abnormalities
• Influenza Cerebellitis in a 3-Year-Old Male
• Intracranial vasculopathy: an important organ damage in young adult patients with late-onset Pompe disease
• Is unilateral cerebellum sufficient? Insights from new cases of cerebellar agenesis and literature review
• Longitudinal Changes of Clinical, Imaging, and Fluid Biomarkers in Preataxic and Early Ataxic Spinocerebellar Ataxia Type 2 and 7 Carriers
• Mapping macrostructural and microstructural brain alterations in patients with neuronal intranuclear inclusion disease
• Microcornea, cerebellar hypoplasia and hyperlax joints-unusual combo in rare Ehlers-Danlos syndrome-musculocontractural type 1
• Microstructural evaluation of the brain with advanced magnetic resonance imaging techniques in cases of electrical status epilepticus during sleep (ESES)
• Monoallelic missense variants in <em>MAB21L1</em> cause a novel autosomal dominant microphthalmia
• MRI in LARS1 deficiency-Spectrum, patterns, and correlation with acute neurological deterioration
• Mutations in Genes Encoding Subunits of the RNA Exosome as a Potential Novel Cause of Thrombotic Microangiopathy
• Neuroanatomical Features of NAA10- and NAA15-Related Neurodevelopmental Syndromes
• Neurodevelopmental profiles of 14 individuals with phosphomannomutase deficiency (PMM2-CDG)
• Neuroinflammation and Lysosomal Abnormalities Characterise the Essential Role for Oxidation Resistance 1 in the Developing and Adult Cerebellum
• Neurophysiological and brain structural insights into cyclin-dependent kinase-like 5 deficiency disorder: Visual and auditory evoked potentials and MRI analysis
• New clues for the role of cerebellum in schizophrenia and the associated cognitive impairment
• Non-hemorrhagic cerebellar contrast enhancement on intraoperative MRI during a supratentorial glioma resection: Concerning finding of no significance
• Oculomotor and Vestibular Deficits in Friedreich Ataxia - Systematic Review and Meta-Analysis of Quantitative Measurements
• Optimal prenatal genetic diagnostic approach for posterior fossa malformation: karyotyping, copy number variant testing, or whole-exome sequencing?
• Optimizing Rare Disease Gait Classification through Data Balancing and Generative AI: Insights from Hereditary Cerebellar Ataxia
• Paraneoplastic syndromes in patients with melanoma
• Passing the torch: The ascendance of the glutamatergic synapse in the pathophysiology of schizophrenia
• Pattern of abnormalities on gray matter in patients with medial temporal lobe epilepsy and hippocampal sclerosis: An updated meta-analysis
• Phenotypic and mutational spectrum of 17 Chinese patients with Menkes Disease
• Pontocerebellar Hypoplasia Type 9: A New Case with a Novel Mutation and Review of Literature
• Prenatal diagnosis of a 15q24.1 microdeletion in a fetus with cerebral and urogenital abnormalities
• Prenatal diagnosis of a fetus with Rubinstein-Taybi syndrome
• Prenatal Diagnosis of Fryns Syndrome through Identification of Two Novel Splice Variants in the <em>PIGN</em> Gene-A Case Series
• Prenatal diagnosis of Joubert syndrome: A case report
• Primary cilia formation requires the Leigh syndrome-associated mitochondrial protein NDUFAF2
• Pro-atherogenic medical conditions are associated with widespread regional brain metabolite abnormalities in those with alcohol use disorder
• Protective effect of cholecalciferol against cobalt-induced neurotoxicity in rats: ZO-1/iFABP, ChAT/AchE and antioxidant pathways as potential therapeutic targets
• Rate of abnormalities in quantitative MR neuroimaging of persons with chronic traumatic brain injury
• Regional brain activity and connectivity associated with childhood trauma in drug-naive patients with obsessive-compulsive disorder
• Retinal structural thicknesses reflect clinically relevant microstructural white matter abnormalities in neuromyelitis optica spectrum disorders
• Ruptured Anterior Inferior Cerebellar Artery Aneurysm From a Persistent Trigeminal Artery: A Case Report
• Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs
• SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X-Linked Intellectual Disability
• Structural and functional abnormalities and cognitive profiles in older adults with early-onset and late-onset focal epilepsy
• Survival-Related Genes on Chromosomes 6 and 17 in Medulloblastoma
• T1w/T2w ratio maps identify children with autism spectrum disorder and the relationships between myelin-related changes and symptoms
• The characteristic and biomarker value of transcranial sonography in cerebellar ataxia
• The clinical and predictive value of ¹⁸F-FDG PET/CT metabolic patterns in a clinical Chinese cohort with autoimmune encephalitis
• The crucial role of the cerebellum in autism spectrum disorder: Neuroimaging, neurobiological, and anatomical insights
• The impact of an anomalous third segment of the vertebral artery on bypass surgery: a case report and literature review
• Tribal Founder <em>EMC1</em> Variant in 5 Kuwaiti Families Expands Phenotypic Spectrum of <em>EMC1</em>-Related Disorder
• Ultra-High Contrast MRI: The Whiteout Sign Shown with Divided Subtracted Inversion Recovery (dSIR) Sequences in Post-Insult Leukoencephalopathy Syndromes (PILS)
• Volumetric and diffusion MRI abnormalities associated with dysarthria in multiple sclerosis
• White Matter Abnormalities Track Disease Progression in Multiple System Atrophy