Abnormal DaTscan in GM1-Gangliosidosis Type III Manifesting with Dystonia-Parkinsonism

MOVEMENT DISORDERS CLINICAL PRACTICE(2022)

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Movement Disorders Clinical PracticeVolume 9, Issue 6 p. 825-828 CASE REPORT Abnormal DaTscan in GM1-Gangliosidosis Type III Manifesting with Dystonia-Parkinsonism Shahedah Koya Kutty MD, MRCP, Shahedah Koya Kutty MD, MRCP orcid.org/0000-0003-2015-4691 Department of Medicine, Faculty of Medicine, International Islamic University Malaysia (IIUM), Kuantan, Malaysia Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United KingdomSearch for more papers by this authorFrancesca Magrinelli MD, PhD, Francesca Magrinelli MD, PhD orcid.org/0000-0003-4706-6245 Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United KingdomSearch for more papers by this authorAnna Vera Milner MD,, Anna Vera Milner MD, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United KingdomSearch for more papers by this authorKailash P. Bhatia MD, DM, FRCP,, Corresponding Author Kailash P. Bhatia MD, DM, FRCP, k.bhatia@ucl.ac.uk orcid.org/0000-0001-8185-286X Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom Correspondence to: Prof. Kailash P. Bhatia, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, Queen Square, London WC1N 3BG, United Kingdom; E-mail: k.bhatia@ucl.ac.ukSearch for more papers by this author Shahedah Koya Kutty MD, MRCP, Shahedah Koya Kutty MD, MRCP orcid.org/0000-0003-2015-4691 Department of Medicine, Faculty of Medicine, International Islamic University Malaysia (IIUM), Kuantan, Malaysia Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United KingdomSearch for more papers by this authorFrancesca Magrinelli MD, PhD, Francesca Magrinelli MD, PhD orcid.org/0000-0003-4706-6245 Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United KingdomSearch for more papers by this authorAnna Vera Milner MD,, Anna Vera Milner MD, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United KingdomSearch for more papers by this authorKailash P. Bhatia MD, DM, FRCP,, Corresponding Author Kailash P. Bhatia MD, DM, FRCP, k.bhatia@ucl.ac.uk orcid.org/0000-0001-8185-286X Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom Correspondence to: Prof. Kailash P. Bhatia, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, Queen Square, London WC1N 3BG, United Kingdom; E-mail: k.bhatia@ucl.ac.ukSearch for more papers by this author First published: 22 June 2022 https://doi.org/10.1002/mdc3.13512Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat Volume9, Issue6August 2022Pages 825-828 RelatedInformation
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beta-galactosidase, DaTscan, GLB1, lysosomal storage disorder, nigrostriatal degeneration
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