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Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study.
Kurian MA, Li Y, Zhen J, Meyer E, Hai N, Christen HJ, Hoffmann GF, Jardine P, von Moers A, Mordekar SR, O'Callaghan F, Wassmer E, Wraige E, Dietrich C, Lewis T, Hyland K, Heales S Jr, Sanger T, Gissen P, Assmann BE, Reith ME, Maher ER. Kurian MA, et al. Among authors: sanger t. Lancet Neurol. 2011 Jan;10(1):54-62. doi: 10.1016/S1474-4422(10)70269-6. Epub 2010 Nov 25. Lancet Neurol. 2011. PMID: 21112253 Free PMC article.
Advances in management of movement disorders in children.
Koy A, Lin JP, Sanger TD, Marks WA, Mink JW, Timmermann L. Koy A, et al. Lancet Neurol. 2016 Jun;15(7):719-735. doi: 10.1016/S1474-4422(16)00132-0. Epub 2016 May 9. Lancet Neurol. 2016. PMID: 27302239 Review.
Pediatric movement disorders.
Sanger TD. Sanger TD. Curr Opin Neurol. 2003 Aug;16(4):529-35. doi: 10.1097/01.wco.0000084233.82329.0e. Curr Opin Neurol. 2003. PMID: 12869814 Review.
Definition and classification of hyperkinetic movements in childhood.
Sanger TD, Chen D, Fehlings DL, Hallett M, Lang AE, Mink JW, Singer HS, Alter K, Ben-Pazi H, Butler EE, Chen R, Collins A, Dayanidhi S, Forssberg H, Fowler E, Gilbert DL, Gorman SL, Gormley ME Jr, Jinnah HA, Kornblau B, Krosschell KJ, Lehman RK, MacKinnon C, Malanga CJ, Mesterman R, Michaels MB, Pearson TS, Rose J, Russman BS, Sternad D, Swoboda KJ, Valero-Cuevas F. Sanger TD, et al. Mov Disord. 2010 Aug 15;25(11):1538-49. doi: 10.1002/mds.23088. Mov Disord. 2010. PMID: 20589866 Free PMC article. Review.
237 results