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Broadening the Spectrum of SLC22A5 Phenotype: Primary Carnitine Deficiency Presenting with Focal Myoclonus.
Khries, Maymunah; Lim, Albert; Mitra, Dipayan; Anderson, Mark; Bengtsson, Jan; Bowron, Ann; Harris, Elizabeth; Blickwedel, Jessica; Wood, Karen; Basu, Anna P.
Afiliación
  • Khries M; Paediatric Neurology, Great North Children's Hospital, Newcastle upon Tyne, UK.
  • Lim A; Paediatric Neurology, Great North Children's Hospital, Newcastle upon Tyne, UK.
  • Mitra D; Neuroradiology, Great North Children's Hospital, Newcastle upon Tyne, UK.
  • Anderson M; Paediatrics, Great North Children's Hospital, Newcastle upon Tyne, UK.
  • Bengtsson J; Paediatric Intensive Care Unit, Great North Children's Hospital, Newcastle upon Tyne, UK.
  • Bowron A; Metabolic Biochemistry, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Harris E; Northern Genetics Service, Centre for Life, Newcastle upon Tyne, UK.
  • Blickwedel J; Paediatric Neurology, Great North Children's Hospital, Newcastle upon Tyne, UK.
  • Wood K; Paediatric Neurology, Great North Children's Hospital, Newcastle upon Tyne, UK.
  • Basu AP; Paediatric Neurology, Great North Children's Hospital, Newcastle upon Tyne, UK.
Child Neurol Open ; 10: 2329048X231184183, 2023.
Article en En | MEDLINE | ID: mdl-37475835
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Child Neurol Open Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Child Neurol Open Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos