Intervention Protocol

Treatment for dysphagia (swallowing difficulties) in hereditary ataxia syndromes

  1. Adam P Vogel1,*,
  2. Ellika Schalling2,
  3. Joanne Folker3,
  4. Kerstin Johansson2

Editorial Group: Cochrane Neuromuscular Disease Group

Published Online: 17 OCT 2012

DOI: 10.1002/14651858.CD010169


How to Cite

Vogel AP, Schalling E, Folker J, Johansson K. Treatment for dysphagia (swallowing difficulties) in hereditary ataxia syndromes (Protocol). Cochrane Database of Systematic Reviews 2012, Issue 10. Art. No.: CD010169. DOI: 10.1002/14651858.CD010169.

Author Information

  1. 1

    University of Melbourne, Speech Neuroscience Unit, Melbourne Medical School, Melbourne, Victoria, Australia

  2. 2

    Karolinska Institutet, Department of Clinical Science, Intervention and Technology, Division of Speech and Language Pathology, Stockholm, Sweden

  3. 3

    The University of Queensland, School of Health and Rehabilitation Sciences, Brisbane, Australia

*Adam P Vogel, Speech Neuroscience Unit, Melbourne Medical School, University of Melbourne, 550 Swanston Street, Parkville, Melbourne, Victoria, 3010, Australia. vogela@unimelb.edu.au.

Publication History

  1. Publication Status: New
  2. Published Online: 17 OCT 2012

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