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Pathophysiology of motor dysfunction in a childhood motor neuron disease caused by mutations in the riboflavin transporter.
Menezes, Manoj P; Farrar, Michelle A; Webster, Richard; Antony, Jayne; O'Brien, Katherine; Ouvrier, Robert; Kiernan, Matthew C; Burns, Joshua; Vucic, Steve.
Affiliation
  • Menezes MP; Institute for Neuroscience and Muscle Research, The Children's Hospital at Westmead, Sydney, Australia; Discipline of Paediatrics and Child Health, The Children's Hospital at Westmead Clinical School, The University of Sydney, Sydney, Australia; Department of Neurology, The Children's Hospital at We
  • Farrar MA; Discipline of Paediatrics, School of Women's and Children's Health, UNSW Medicine, The University of New South Wales, Sydney, Australia; Neurosciences Research Australia, Sydney, Australia; Department of Neurology, Sydney Children's Hospital, Sydney, Australia. Electronic address: m.farrar@unsw.edu.
  • Webster R; Institute for Neuroscience and Muscle Research, The Children's Hospital at Westmead, Sydney, Australia; Department of Neurology, The Children's Hospital at Westmead, Sydney, Australia.
  • Antony J; Department of Neurology, The Children's Hospital at Westmead, Sydney, Australia.
  • O'Brien K; Department of Audiology, The Children's Hospital at Westmead, Sydney, Australia.
  • Ouvrier R; Institute for Neuroscience and Muscle Research, The Children's Hospital at Westmead, Sydney, Australia; Discipline of Paediatrics and Child Health, The Children's Hospital at Westmead Clinical School, The University of Sydney, Sydney, Australia; Department of Neurology, The Children's Hospital at We
  • Kiernan MC; Neurosciences Research Australia, Sydney, Australia; Sydney Medical School, Brain & Mind Research Institute, University of Sydney, Sydney, Australia.
  • Burns J; Institute for Neuroscience and Muscle Research, The Children's Hospital at Westmead, Sydney, Australia; Paediatric Gait Analysis Service of New South Wales, Sydney Children's Hospitals Network, Sydney, Australia; Sydney Arthritis and Musculoskeletal Research Network, The University of Sydney, Sydney
  • Vucic S; Department of Neurology, Westmead Hospital and Western Clinical School, University of Sydney, Sydney, Australia.
Clin Neurophysiol ; 127(1): 911-918, 2016 Jan.
Article in En | MEDLINE | ID: mdl-26092362
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Full text: 1 Database: MEDLINE Main subject: Bulbar Palsy, Progressive / Membrane Transport Proteins / Receptors, G-Protein-Coupled / Hearing Loss, Sensorineural / Mutation Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Language: En Journal: Clin Neurophysiol Year: 2016 Type: Article
Fulltext
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Full text: 1 Database: MEDLINE Main subject: Bulbar Palsy, Progressive / Membrane Transport Proteins / Receptors, G-Protein-Coupled / Hearing Loss, Sensorineural / Mutation Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Language: En Journal: Clin Neurophysiol Year: 2016 Type: Article