Cerebellar Diseases

• 

  Subject Areas on Research

  • A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition. 
  • Alternating hemiplegia of childhood. 
  • Anteroinferior cerebellar artery aneurysms: surgical approaches and outcomes--a review of 34 cases. 
  • Atypical imaging findings in a near-fatal case of posterior reversible encephalopathy syndrome in a child. 
  • Behavioral Deficits at 18-22 Months of Age Are Associated with Early Cerebellar Injury and Cognitive and Language Performance in Children Born Extremely Preterm. 
  • Carcinomatous cerebellar degeneration, encephalomyelitis, and sensory neuropathy (radiculitis). Report of a case incorporating both purely degenerative and intense inflammatory changes, with special prominence of the latter in the putamen. 
  • Cerebellar cryptococcoma in a patient with undiagnosed sarcoidosis: case report. 
  • Cerebellar defects in Ca2+/calmodulin kinase IV-deficient mice. 
  • Cerebellar hemorrhage after spinal surgery: report of two cases and literature review. 
  • Cerebellar hemorrhage from a delayed cervical spine hardware migration. 
  • Evolutionarily assembled cis-regulatory module at a human ciliopathy locus. 
  • Familial spinocerebellar degeneration with corneal dystrophy. 
  • Genetics of cerebral cavernous malformations. 
  • Improved survival in the largest national cohort of adults with cerebellar versus supratentorial low-grade astrocytomas. 
  • Inflammatory lesion mimicking a metastatic ependymoma. 
  • Intracranial pressure and hemodynamic effects of remifentanil versus alfentanil in patients undergoing supratentorial craniotomy. 
  • Late onset of distinct neurologic syndromes in galactosemic siblings. 
  • Latitudinal variation in incidence and type of first central nervous system demyelinating events. 
  • Limited regional cerebellar dysfunction induces focal dystonia in mice. 
  • Mutations in CSPP1, encoding a core centrosomal protein, cause a range of ciliopathy phenotypes in humans. 
  • Neurocognitive outcome 12 months following cerebellar mutism syndrome in pediatric patients with medulloblastoma. 
  • Neurotologic management of intracranial epidermoid tumors. 
  • Ocular reactions in man from deep cerebellar stimulation and lesions. 
  • Persistent figure-eight and side-to-side head shaking is a marker for rhombencephalosynapsis. 
  • Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders. 
  • Pontocerebellar hypoplasia, malignant hyperthermia, and inappropriate use of secondary references. 
  • Posterior fossa abnormalities in major depression: a controlled magnetic resonance imaging study. 
  • Postradiation cerebellar necrosis mimicking tumor: MR appearance. 
  • Senataxin, A Novel Helicase at the Interface of RNA Transcriptome Regulation and Neurobiology: From Normal Function to Pathological Roles in Motor Neuron Disease and Cerebellar Degeneration. 
  • TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone. 
  • Upward transtentorial herniation, hydrocephalus, and cerebellar edema in hypertensive encephalopathy. 
• 

  Keywords of People

  • Davis, Erica Ellen, Associate Professor of Pediatrics, Cell Biology
  • Warner, David Samuel, Distinguished Professor of Anesthesiology, in the School of Medicine, Neurobiology