Book contents
- Case Studies in Movement Disorders
- Case Studies in Movement Disorders
- Copyright page
- Contents
- Video Captions
- Contributors
- Preface
- Previously Published Cases
- Abbreviations
- Section 1 Parkinsonism
- Section 2 Dystonia
- Section 3 Tics
- Section 4 Chorea
- Section 5 Tremor
- Section 6 Myoclonus
- Section 7 Ataxia
- Index
- Plate section
- References
Section 7 - Ataxia
Published online by Cambridge University Press: 04 July 2017
Book contents
- Case Studies in Movement Disorders
- Case Studies in Movement Disorders
- Copyright page
- Contents
- Video Captions
- Contributors
- Preface
- Previously Published Cases
- Abbreviations
- Section 1 Parkinsonism
- Section 2 Dystonia
- Section 3 Tics
- Section 4 Chorea
- Section 5 Tremor
- Section 6 Myoclonus
- Section 7 Ataxia
- Index
- Plate section
- References
Summary
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- Type
- Chapter
- Information
- Case Studies in Movement DisordersCommon and Uncommon Presentations, pp. 134 - 150Publisher: Cambridge University PressPrint publication year: 2017
References
Suggested Readings
Rossi, M, Perez-Lloret, S, Cerquetti, D, et al. Movement disorders in autosomal dominant cerebellar aaxias: a systematic review. Mov Disord Clin Pract. 2014;1:154–60.CrossRefGoogle ScholarPubMed
Solodkin, A, Gomez, CM. Spinocerebellar ataxia type 6. Handb Clin Neurol. 2012;103:461–73.CrossRefGoogle ScholarPubMed
Suggested Readings
Lin, DJ, Hermann, KL, Schmahmann, JD. Multiple system atrophy of the cerebellar type: clinical state of the art. Mov Disord. 2014;29:294–304.CrossRefGoogle ScholarPubMed
Wenning, GK, Kraft, E, Beck, RW, et al. Cerebellar presentation of multiple system atrophy. Mov Disord. 1997;12:115–17.Google ScholarPubMed
Suggested Readings
Apartis, E, Blancher, A, Meissner, WG, et al. FXTAS: new insights and the need for revised diagnostic criteria. Neurology. 2012;79:1898–907.CrossRefGoogle ScholarPubMed
Kamm, C, Healy, DG, Quinn, NP, et al. The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group. Brain. 2005;128(Pt 8):1855–60.CrossRefGoogle ScholarPubMed
Renaud, M, Perriard, J, Coudray, S, et al. Relevance of corpus callosum splenium versus middle cerebellar peduncle hyperintensity for FXTAS diagnosis in clinical practice. J Neurol. 2015;262:435–42.CrossRefGoogle ScholarPubMed
Suggested Readings
Hanisch, F, Kornhuber, M, Alston, CL, Taylor, RW, Deschauer, M, Zierz, S. SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions. J Neurol Neurosurg Psychiatry. 2015;86:630–4.CrossRefGoogle Scholar
Milone, M, Massie, R. Polymerase gamma 1 mutations: clinical correlations. Neurologist. 2010;16:84–91.CrossRefGoogle ScholarPubMed
Suggested Readings
Charlesworth, G, Mohire, MD, Schneider, SA, Stamelou, M, Wood, NW, Bhatia, KP. Ataxia telangiectasia presenting as dopa-responsive cervical dystonia. Neurology. 2013;81:1148–51.Google Scholar
Chun, HH, Gatti, RA. Ataxia-telangiectasia, an evolving phenotype. DNA Repair (Amst). 2004;3:1187–96.CrossRefGoogle ScholarPubMed
Méneret, A, Ahmar-Beaugendre, Y, Rieunier, G, et al. The pleiotropic movement disorders phenotype of adult ataxia-telangiectasia. Neurology. 2014;83:1087–95.CrossRefGoogle ScholarPubMed
Suggested Readings
Höftberger, R, Rosenfeld, MR, Dalmau, J. Update on neurological paraneoplastic syndromes. Curr Opin Oncol. 2015;27:489–95.CrossRefGoogle ScholarPubMed
Mitoma, H, Hadjivassiliou, M, Honnorat, J. Guidelines for treatment of immune-mediated cerebellar ataxias. Cerebellum Ataxias. 2015;2:14.CrossRefGoogle ScholarPubMed
Suggested Readings
Durr, A. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond. Lancet Neurol. 2010;9:885–94.CrossRefGoogle ScholarPubMed
Jacobi, H, Bauer, P, Giunti, P, et al. The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study. Neurology. 2011;77:1035–41.CrossRefGoogle ScholarPubMed
Nakano, KK, Dawson, DM, Spence, A. Machado disease: a hereditary ataxia in Portuguese immigrants to Massachusetts. Neurology. 1972;22:49–55.CrossRefGoogle Scholar
Suggested Readings
Mengel, E, Klünemann, HH, Lourenço, CM, et al. Niemann-Pick disease type C symptomatology: an expert-based clinical description. Orphanet J Rare Dis. 2013;8:166.CrossRefGoogle ScholarPubMed
Patterson, MC, Hendriksz, CJ, Walterfang, M, Sedel, F, Vanier, MT, Wijburg, F. Recommendations for the diagnosis and management of Niemann-Pick disease type C: an update. Mol Genet Metab. 2012;106:330–44.CrossRefGoogle ScholarPubMed
Sévin, M, Lesca, G, Baumann, N, et al. The adult form of Niemann-Pick disease type C. Brain. 2007;130:120–33.Google ScholarPubMed