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Surveillance for variant CJD: should more children with neurodegenerative diseases have autopsies?
Verity, Christopher; Winstone, Anne Marie; Will, Robert; Powell, Alison; Baxter, Peter; de Sousa, Carlos; Gissen, Paul; Kurian, Manju; Livingston, John; McFarland, Robert; Pal, Suvankar; Pike, Michael; Robinson, Richard; Wassmer, Evangeline; Zuberi, Sameer.
Afiliación
  • Verity C; PIND Research Group, Addenbrooke's Hospital, Cambridge, UK.
  • Winstone AM; PIND Research Group, Addenbrooke's Hospital, Cambridge, UK.
  • Will R; The National Creutzfeldt-Jakob Disease Research and Surveillance Unit, Western General Hospital, Edinburgh, UK.
  • Powell A; PIND Research Group, Addenbrooke's Hospital, Cambridge, UK.
  • Baxter P; Paediatric Neurology Department, Sheffield Children's NHS Foundation Trust, Sheffield, UK.
  • de Sousa C; Neurology Department, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Gissen P; Neurology Department, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Kurian M; Institute of Child Health, Great Ormond Street Hospital for Children, London, UK.
  • Livingston J; Paediatric Neurology Department, Leeds General Infirmary, Leeds, UK.
  • McFarland R; Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, The Medical School, Newcastle upon Tyne, UK.
  • Pal S; The National Creutzfeldt-Jakob Disease Research and Surveillance Unit, Western General Hospital, Edinburgh, UK.
  • Pike M; Paediatric Neurology Department, Oxford Children's Hospital, John Radcliffe Hospital site, Oxford, UK.
  • Robinson R; Paediatric Neurology Department, Guy's Hospital, London, UK.
  • Wassmer E; Paediatric Neurology Department, Birmingham Children's Hospital, Birmingham, UK.
  • Zuberi S; Paediatric Neurosciences Research Group, Royal Hospital for Children and School of Medicine, University of Glasgow, Glasgow, UK.
Arch Dis Child ; 104(4): 360-365, 2019 04.
Article en En | MEDLINE | ID: mdl-30337492
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Creutzfeldt-Jakob / Enfermedades Neurodegenerativas Tipo de estudio: Prognostic_studies / Screening_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País/Región como asunto: Europa Idioma: En Revista: Arch Dis Child Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Creutzfeldt-Jakob / Enfermedades Neurodegenerativas Tipo de estudio: Prognostic_studies / Screening_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País/Región como asunto: Europa Idioma: En Revista: Arch Dis Child Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido