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Title of Journal: Cerebellum

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Abbravation: The Cerebellum

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Springer-Verlag

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DOI

10.1002/nadc.19640122203

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1473-4230

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Cerebellar Function in Developmental Dyslexia

Authors: Catherine J Stoodley John F Stein
Publish Date: 2012/08/01
Volume: 12, Issue: 2, Pages: 267-276
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Abstract

Developmental dyslexia is a genetically based neurobiological syndrome which is characterized by reading difficulty despite normal or high general intelligence Even remediated dyslexic readers rarely achieve fast fluent reading Some dyslexics also have impairments in attention shortterm memory sequencing letters word sounds and motor acts eye movements poor balance and general clumsiness The presence of “cerebellar” motor and fluency symptoms led to the proposal that cerebellar dysfunction contributes to the etiology of dyslexia Supporting this functional imaging studies suggest that the cerebellum is part of the neural network supporting reading in typically developing readers and reading difficulties have been reported in patients with cerebellar damage Differences in both cerebellar asymmetry and gray matter volume are some of the most consistent structural brain findings in dyslexics compared with good readers Furthermore cerebellar functional activation patterns during reading and motor learning can differ in dyslexic readers Behaviorally some children and adults with dyslexia show poorer performance on cerebellar motor tasks including eye movement control postural stability and implicit motor learning However many dyslexics do not have cerebellar signs many cerebellar patients do not have reading problems and differences in dyslexic brains are found throughout the whole reading network and not isolated to the cerebellum Therefore impaired cerebellar function is probably not the primary cause of dyslexia but rather a more fundamental neurodevelopmental abnormality leads to differences throughout the reading network


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Other Papers In This Journal:

  1. Cerebellum: from Fundamentals to Translational Approaches. The Seventh International Symposium of the Society for Research on the Cerebellum
  2. Cerebellar Contribution to Anger Recognition Deficits in Huntington’s Disease
  3. T-Type Calcium Channel as a New Therapeutic Target for Tremor
  4. Compartmentation of the Cerebellar Cortex in the Naked Mole-Rat ( Heterocephalus glaber )
  5. Behavioural Significance of Cerebellar Modules
  6. An fMRI Investigation of Cerebellar Function During Verbal Working Memory in Methadone Maintenance Patients
  7. Neurofilament Heavy Chain Expression Reveals a Unique Parasagittal Stripe Topography in the Mouse Cerebellum
  8. Regional Cerebellar Volumes Predict Functional Outcome in Children with Cerebellar Malformations
  9. Predictive Motor Timing Performance Dissociates Between Early Diseases of the Cerebellum and Parkinson's Disease
  10. A Cerebellar Framework for Predictive Coding and Homeostatic Regulation in Depressive Disorder
  11. Spinal Cord Atrophy Correlates with Disability in Friedreich’s Ataxia
  12. High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression
  13. High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression
  14. Recessive Spinocerebellar Ataxia with Paroxysmal Cough Attacks: A Report of Five Cases
  15. Cerebellum and Personality Traits
  16. Development of External Surfaces of Human Cerebellar Lobes in the Fetal Period
  17. Friedreich's Ataxia Causes Redistribution of Iron, Copper, and Zinc in the Dentate Nucleus
  18. Increased Catabolic State in Spinocerebellar Ataxia Type 1 Patients
  19. Mild Clinical and Biochemical Phenotype in Two Patients with PMM2-CDG (Congenital Disorder of Glycosylation Ia)
  20. Glutamate Dysfunction Associated with Developmental Cerebellar Damage: Relevance to Autism Spectrum Disorders
  21. Non-Ataxic Presenting Symptoms of Dominant Ataxias
  22. Asymmetries in Cerebellar Plasticity and Motor Learning
  23. Clinical Manifestations of Cerebellar Infarction According to Specific Lobular Involvement

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