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Early white matter involvement in an infant carrying a novel mutation in ACOX1.
Masson, R; Guerra, S; Cerini, R; Pensato, V; Gellera, C; Taroni, F; Simonati, A.
Affiliation
  • Masson R; Department of Neuroscience, Biomedicine, Movement-Neurology (Child Neurology and Psychiatry), University of Verona, Italy.
  • Guerra S; Department of Neuroscience, Biomedicine, Movement-Neurology (Child Neurology and Psychiatry), University of Verona, Italy.
  • Cerini R; Radiology Unit, Bussolengo Hospital, AUSL22 Regione Veneto, Italy.
  • Pensato V; Unit of Genetics of Neurodegenerative and Metabolic Disease, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Gellera C; Unit of Genetics of Neurodegenerative and Metabolic Disease, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Taroni F; Unit of Genetics of Neurodegenerative and Metabolic Disease, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Simonati A; Department of Neuroscience, Biomedicine, Movement-Neurology (Child Neurology and Psychiatry), University of Verona, Italy. Electronic address: alessandro.simonati@univr.it.
Eur J Paediatr Neurol ; 20(3): 431-4, 2016 May.
Article in En | MEDLINE | ID: mdl-26965209
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Seizures / Acyl-CoA Oxidase / White Matter / Mutation Type of study: Prognostic_studies Limits: Child, preschool / Humans / Infant / Male Language: En Journal: Eur J Paediatr Neurol Year: 2016 Document type: Article
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Seizures / Acyl-CoA Oxidase / White Matter / Mutation Type of study: Prognostic_studies Limits: Child, preschool / Humans / Infant / Male Language: En Journal: Eur J Paediatr Neurol Year: 2016 Document type: Article