Disease: Cerebellar agenesis
- <em>ATP1A3</em> Disease Spectrum Includes Paroxysmal Weakness and Encephalopathy Not Triggered by Fever
- A de novo pathogenic variant in DHX30 gene in a fetus with isolated dysgenesis of the corpus callosum
- A missense mutation in the <em>Hspa8</em> gene encoding heat shock cognate protein 70 causes neuroaxonal dystrophy in rats
- A novel ACTB variant in an atypical case of Baraitser-Winter syndrome with cerebellar hypoplasia and diaphragmatic hernia
- Abnormalities in signal transduction of Purkinje cells in spinocerebellar ataxias: a review
- Abnormality of Early White Matter Development in Tuberous Sclerosis Complex and Autism Spectrum Disorder: Longitudinal Analysis of Diffusion Tensor Imaging Measures
- ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel-Van der Aa syndrome autopsy case
- Alterations in degree centrality and functional connectivity in tension-type headache: a resting-state fMRI study
- Alterations of the cerebral microstructure in patients with noise-induced hearing loss: A diffusion tensor imaging study
- Altered Resting-State Amygdalar Functional Connectivity in Primary Angle-Closure Glaucoma Patients
- Altered static and dynamic cerebellar-cerebral functional connectivity in acute pontine infarction
- Altered static and dynamic functional brain network in knee osteoarthritis: A resting-state functional magnetic resonance imaging study
- Altered static and dynamic functional brain network in knee osteoarthritis: A resting-state functional magnetic resonance imaging study: Static and dynamic FNC in KOA
- Assessment of brain structure and volume reveals neurodevelopmental abnormalities in preterm infants with low-grade intraventricular hemorrhage
- Association of abnormal explicit sense of agency with cerebellar impairment in myoclonus-dystonia
- ATXN7-Related Cone-Rod Dystrophy: The Integrated Functional Evaluation of the Cerebellum (CERMOI) Study
- Brain function in classic galactosemia, a galactosemia network (GalNet) members review
- Brain Structural and Functional Abnormalities Associated with Acute Post-Traumatic Headache: Iron Deposition and Functional Connectivity
- Case report: A new de novo 6q21q22.1 interstitial deletion case in a girl with cerebellar vermis hypoplasia and developmental delay and literature review
- Cerebellum Purkinje cell vulnerability in aged rats with memory impairment
- Characteristics of Developmental and Epileptic Encephalopathy Associated with <em>PACS2</em> p.Glu209Lys Pathogenic Variant-Our Experience and Systematic Review of the Literature
- CHD8-related disorders redefined: an expanding spectrum of dystonic phenotypes
- Clinical and Imaging Profile of Patients with Cerebrotendinous Xanthomatosis - a Video Case Series from India
- Clinical and Molecular Characteristics of Neuronal Ceroid Lipofuscinosis in Saudi Arabia
- Clinical and neurogenetic characterisation of autosomal recessive RBL2-associated progressive neurodevelopmental disorder
- CMV-induced Hearing Loss
- Cognitive outcome and its neural correlates after cardiorespiratory arrest in childhood
- Contribution of the serotonergic system to developmental brain abnormalities in autism spectrum disorder
- Cortical-cerebellar circuits changes in preschool ASD children by multimodal MRI
- Dandy Walker variant with agenesis of corpus callosum diagnosed late prenatally by foetal ultrasound: a case report
- Diagnosis of Delayed Post-Hypoxic Leukoencephalopathy (Grinker's Myelinopathy) with MRI Using Divided Subtracted Inversion Recovery (dSIR) Sequences: Time for Reappraisal of the Syndrome?
- Direct Implantation of Patient Brain Tumor Cells into Matching Locations in Mouse Brains for Patient-Derived Orthotopic Xenograft Model Development
- Disproportion of Corpus Callosum in Fetuses With Malformations of Cortical Development
- Divergent growth of the transient brain compartments in fetuses with nonsyndromic isolated clefts involving the primary and secondary palate
- Dual and opposing roles for the kinesin-2 motor, KIF17, in Hedgehog-dependent cerebellar development
- Effects of cortisol administration on heart rate variability and functional connectivity across women with different depression histories
- Effects of mini-basketball training program on social communication impairments and regional homogeneity of brain functions in preschool children with autism spectrum disorder
- Evaluation and Treatment of Patients with Small Posterior Cranial Fossa and Chiari Malformation, Types 0 and 1
- Expression changes of RNA m6A regulators in mouse cerebellum affected by hypobaric hypoxia stimulation
- Fanconi Anemia Neuroinflammatory Syndrome (FANS): Brain Lesions and Neurologic Injury in Fanconi Anemia
- Fast field echo resembling CT using restricted echo-spacing (FRACTURE) MR sequence can provide craniocervical region images comparable to a CT in dogs
- Fetal agenesis of the corpus callosum: Clinical and genetic analysis in a series of 40 patients
- Functional and structural effects of repetitive transcranial magnetic stimulation (rTMS) for the treatment of auditory verbal hallucinations in schizophrenia: A systematic review
- Functional connectivity changes of the hippocampal subregions in anti-N-methyl-D-aspartate receptor encephalitis
- Functional Connectivity of Language-Related Cerebellar Regions Is Reduced in Schizophrenia Patients
- Functional neuroimaging in patients with catatonia: A systematic review
- Generation and characterization of cerebellar granule neurons specific knockout mice of Golli-MBP
- Genotype-phenotype correlation in CLCN4-related developmental and epileptic encephalopathy
- Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study
- Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study
- High Incidence of <em>CPLANE1</em>-Related Joubert Syndrome in the Products of Conceptions from Early Pregnancy Losses
- High incidence of cerebrovascular lesions on magnetic resonance imaging in pediatric COVID-19 during omicron outbreak - A retrospective case series
- Historical review: The golden age of the Golgi method in human neuropathology
- Homotopic functional connectivity disruptions in schizophrenia and their associated gene expression
- Homozygous CNP Mutation and Neurodegeneration in Weimaraners: Myelin Abnormalities and Accumulation of Lipofuscin-like Inclusions
- Imaging findings of children with PTEN-related hamartoma tumor syndrome: a 20-year multicentric pediatric cohort
- Insight into the Relationship Between Motor and Cognitive Symptoms in Essential Tremor
- Joubert syndrome presenting bilateral peroneal neuropathies: A case report
- Joubert syndrome-derived induced pluripotent stem cells show altered neuronal differentiation in vitro
- Management of Autoimmune Encephalitis in a 7-Year-Old Child With CTLA-4 Haploinsufficiency and AMPA Receptor Antibodies: A Case Report
- Maternal immunoglobulin G affects brain development of mouse offspring
- Mitochondrial dysfunction in brain tissues and Extracellular Vesicles Fragile X-associated tremor/ataxia syndrome
- Neurodevelopmental trajectories of cerebellar grey matter associated with verbal abilities in males with autism spectrum disorder
- Neuroimaging features of cognitive impairments in schizophrenia and major depressive disorder
- NME3 is a gatekeeper for DRP1-dependent mitophagy in hypoxia
- Novel characterization of <em>CASK</em> variant <em>c.1963 A>G (p.Asn655Asp)</em> through whole-exome sequencing in a monochorionic diamniotic twin fetus with significant brain anomalies: A case report
- Ocular motor and vestibular dysfunction in central nervous system lymphoma
- Oral self-inflicted accidental trauma in patients with neurological disorders: a case report of dental management in infants with cerebellar hypoplasia
- PGAP2-Related Hyperphosphatasia-Mental Retardation Syndrome: Report of a Novel Patient, Toward a Broadening of Phenotypic Spectrum and Therapeutic Perspectives
- PHACE syndrome: a case report and a comprehensive review
- Physiotherapy Rehabilitation Following Acoustic Neuroma Resection in a Patient With Cerebellopontine Angle Tumour: A Case Report
- Placental Pathology Contributes to Impaired Volumetric Brain Development in Neonates With Congenital Heart Disease
- Population-wide cerebellar growth models of children and adolescents
- Posterior cingulate cortex hyperactivity in conversion disorder: a PET/MRI study
- Prenatal Diagnosis of Hemimegalencephaly Using Radiological Methods: A Case Report
- Prenatal diagnosis of non-typical Chiari malformation type I associated with de novo Nuclear Factor I A gene mutation: a case report
- Prevalence and Diagnostic Journey of Friedreich's Ataxia in the State of São Paulo, Brazil
- Progressive ataxia and palatal tremor (PAPT) with hypertrophic olivary degeneration (HOD): A case report
- Promoting Growth in Behavioral Neurology: A Path Forward
- Prosopagnosia Due to Metastatic Brain Tumor: A Case-Based Review
- Psychosis spectrum symptoms among individuals with schizophrenia-associated copy number variants and evidence of cerebellar correlates of symptom severity
- Quantification of Solid Embryonic Cerebellar Graft Volume in a Degenerative Ataxia Model
- RESOLUTION OF CALVARIAL HYPEROSTOSIS IN AFRICAN LION CUBS (<em>PANTHERA LEO LEO</em>) AFTER VITAMIN A SUPPLEMENTATION
- Role of the Cerebellum in Bipolar Disorder: A Systematic Literature Review
- Role of TOE1 variants at the nuclear localization motif in pontocerebellar hypoplasia 7
- Safety considerations in the treatment with anti-CGRP(R) monoclonal antibodies in patients with migraine
- Secondary cerebro-cerebellar and intracerebellar dysfunction in cerebellar mutism syndrome
- Serum S100B protein and white matter changes in schizophrenia before and after medication
- Striatal parvalbumin interneurons are activated in a mouse model of cerebellar dystonia
- Striatal parvalbumin interneurons, not cholinergic interneurons, are activated in a mouse model of cerebellar dystonia
- Structural deviations of the posterior fossa and the cerebellum and their cognitive links in a neurodevelopmental deletion syndrome
- Surgical Treatment of Congenital Kyphosis in Children: Report of a Rare Complication of Remote Cerebellar Haemorrhage
- Syndromic ciliopathy: a taiwanese single-center study
- Systemic lupus erythematosus-related brain abnormalities in the default mode network and the limbic system: A resting-state fMRI meta-analysis
- TBC1D23 mediates Golgi-specific LKB1 signaling
- The thalamic covariance network is associated with cognitive deficits in patients with cerebral small vascular disease
- To explore the potential mechanisms of cognitive impairment in children with MRI-negative pharmacoresistant epilepsy due to focal cortical dysplasia: A pilot study from gray matter structure view
- TRAPPC11-CDG muscular dystrophy: Review of 54 cases including a novel patient
- Typical and atypical MRI abnormalities in Wernicke's encephalopathy: Correlation with blood vitamin B1 levels
- White matter tract integrity in isolated oral clefts: relationship to cognition and reading skills