Pediatric Neurology
Volume 41, Issue 1 , Pages 27-33 , July 2009

Rolandic Mitochondrial Encephalomyelopathy and MT-ND3 Mutations

  • Klaus G.E. Werner, MD, PhD

      Affiliations

    • Division of Neurology and Pediatric Emergency Medicine, Hospital for Sick Children, Toronto, Ontario, Canada
    • Both authors contributed equally to this work.
  • ,
  • Chantal F. Morel, MD

      Affiliations

    • Division of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, Ontario, Canada
    • Both authors contributed equally to this work.
  • ,
  • Adam Kirton, MD

      Affiliations

    • Division of Neurology, Alberta Children's Hospital, Calgary, Alberta, Canada
  • ,
  • Susanne M. Benseler, MD

      Affiliations

    • Division of Rheumatology and Pediatric Emergency Medicine, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada
  • ,
  • John M. Shoffner, MD

      Affiliations

    • Medical Neurogenetics, Atlanta, Georgia
  • ,
  • Jane B.L. Addis, BSc

      Affiliations

    • Metabolism Research Program, Research Institute, Department of Biochemistry, Hospital for Sick Children, Toronto, Ontario, Canada
  • ,
  • Brian H. Robinson, PhD

      Affiliations

    • Metabolism Research Program, Research Institute, Department of Biochemistry, Hospital for Sick Children, Toronto, Ontario, Canada
  • ,
  • Delilah M. Burrowes, MD

      Affiliations

    • Department of Radiology, Northwestern University Feinberg School of Medicine, Chicago, Illinois
  • ,
  • Susan I. Blaser, MD

      Affiliations

    • Department of Diagnostic Imaging, Division of Neuroradiology, Hospital for Sick Children, Toronto, Ontario, Canada
  • ,
  • Leon G. Epstein, MD

      Affiliations

    • Departments of Pediatrics and Neurology, Northwestern University Feinberg School of Medicine, Chicago, Illinois
  • ,
  • Annette S.J. Feigenbaum, MD

      Affiliations

    • Division of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, Ontario, Canada
    • Corresponding Author InformationCommunications should be addressed to: Dr. Feigenbaum; Division of Clinical and Metabolic Genetics; The Hospital for Sick Children; 555 University Avenue; Toronto, Ontario M5G 1X8, Canada.

Received 27 August 2008 ,Accepted 16 February 2009.

References 

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PII: S0887-8994(09)00084-8

doi: 10.1016/j.pediatrneurol.2009.02.010

Pediatric Neurology
Volume 41, Issue 1 , Pages 27-33 , July 2009