Metabolic patterns in brain 18F-fluorodeoxyglucose PET relate to aetiology in paediatric dystonia.

Autor: Tsagkaris, Stavros, Yau, Eric K C, McClelland, Verity, Papandreou, Apostolos, Siddiqui, Ata, Lumsden, Daniel E, Kaminska, Margaret, Guedj, Eric, Hammers, Alexander, Lin, Jean-Pierre

Publikováno v: Brain: A Journal of Neurology; Jun2023, Vol. 146 Issue 6, p2512-2523, 12p

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Metabolic patterns in brain 18F-fluorodeoxyglucose PET relate to aetiology in paediatric dystonia.

Autor: Tsagkaris S; Children's Neurosciences, Complex Motor Disorders Service (CMDS), Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust (GSTT), London SE1 7EH, UK.; King's College London & Guy's and St Thomas' PET Centre, Division of Biomedical Engineering and Imaging Sciences, King's College London, London SE1 7EH, UK., Yau EKC; Department of Paediatrics & Adolescent Medicine, Princess Margaret Hospital, Kowloon, Hong Kong., McClelland V; Children's Neurosciences, Complex Motor Disorders Service (CMDS), Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust (GSTT), London SE1 7EH, UK.; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 8AF, UK., Papandreou A; Children's Neurosciences, Complex Motor Disorders Service (CMDS), Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust (GSTT), London SE1 7EH, UK.; Developmental Neurosciences, Zayed Centre for Research into Rare Disease in Children, University College London Great Ormond Street Institute of Child Health, London WC1N 1DZ, UK., Siddiqui A; Neuroradiology Department, Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust (GSTT), London SE1 7EH, UK., Lumsden DE; Children's Neurosciences, Complex Motor Disorders Service (CMDS), Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust (GSTT), London SE1 7EH, UK.; Perinatal Imaging, Division of Biomedical Engineering and Imaging Sciences, King's College London, London SE1 7EH, UK., Kaminska M; Children's Neurosciences, Complex Motor Disorders Service (CMDS), Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust (GSTT), London SE1 7EH, UK., Guedj E; CERIMED, Nuclear Medicine Department, Aix Marseille Universite, APHM, CNRS, Centrale Marseille, Institut Fresnel, Timone Hospital, 13397 Marseille, France., Hammers A; King's College London & Guy's and St Thomas' PET Centre, Division of Biomedical Engineering and Imaging Sciences, King's College London, London SE1 7EH, UK., Lin JP; Children's Neurosciences, Complex Motor Disorders Service (CMDS), Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust (GSTT), London SE1 7EH, UK.; Women and Children's Health Institute Faculty of Life Sciences & Medicine, Kings Health Partners, King's College London, London SE1 7EH, UK.

Publikováno v: Brain : a journal of neurology [Brain] 2023 Jun 01; Vol. 146 (6), pp. 2512-2523.

A novel mitochondrial DNA deletion in a Chinese girl with Kearns-Sayre syndrome.

Autor: Yau EK; Department of Paediatrics and Adolescent Medicine, Princess Margaret Hospital, Laichikok, Kowloon, Hong Kong. yaukce@hotmail.com, Chan KY, Au KM, Chow TC, Chan YW

Publikováno v: Hong Kong medical journal = Xianggang yi xue za zhi [Hong Kong Med J] 2009 Oct; Vol. 15 (5), pp. 374-7.