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Section 4 - Chorea

Published online by Cambridge University Press:  04 July 2017

Kailash P. Bhatia
Affiliation:
Institute of Neurology, University College London
Roberto Erro
Affiliation:
Università degli Studi di Salerno, Italy
Maria Stamelou
Affiliation:
University of Athens, Greece
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Information
Case Studies in Movement Disorders
Common and Uncommon Presentations
, pp. 80 - 96
Publisher: Cambridge University Press
Print publication year: 2017

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References

Suggested Readings

Gövert, F, Schneider, SA. Huntington’s disease and Huntington’s disease-like syndromes: an overview. Curr Opin Neurol. 2013;26:420–7.CrossRefGoogle ScholarPubMed
Martino, D, Stamelou, M, Bhatia, KP. The differential diagnosis of Huntington’s disease-like syndromes: ‘red flags’ for the clinician. J Neurol Neurosurg Psychiatry. 2013;84(6):650–6.CrossRefGoogle ScholarPubMed
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Suggested Readings

Jung, HH, Danek, A, Walker, RH. Neuroacanthocytosis syndromes. Orphanet J Rare Dis. 2011:25;6:68.CrossRefGoogle Scholar
Martino, D, Stamelou, M, Bhatia, KP. The differential diagnosis of Huntington’s disease-like syndromes: ‘Red flags’ for the clinician. J Neurol Neurosurg Psychiatry. 2013;84(6):650–6.Google Scholar

Suggested Readings

Martino, D, Stamelou, M, Bhatia, KP. The differential diagnosis of Huntington’s disease-like syndromes: ‘red flags’ for the clinician. J Neurol Neurosurg Psychiatry. 2013;84(6):650–6.Google Scholar
Schneider, SA, Walker, RH, Bhatia, KP. The Huntington’s disease-like syndromes: what to consider in patients with a negative Huntington’s disease gene test. Nat Clin Pract Neurol. 2007;3(9):517–25.Google Scholar
Stevanin, G, Brice, A. Spinocerebellar ataxia 17 (SCA17) and Huntington’s disease-like 4 (HDL4). Cerebellum. 2008;7:170–8.CrossRefGoogle ScholarPubMed

Suggested Readings

Hensman Moss, DJ, Poulter, M, Beck, J, et al. C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies. Neurology. 2014;82:292–9.CrossRefGoogle ScholarPubMed
Rohrer, JD, Isaacs, AM, Mizielinska, S, et al. C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis. Lancet Neurol. 2015;14:291301.CrossRefGoogle ScholarPubMed
Wild, EJ, Tabrizi, SJ. Huntington’s disease phenocopy syndromes. Curr Opin Neurol. 2007;20:681–7.Google Scholar

Suggested Readings

Maltese, M, Martella, G, Madeo, G, et al. Anticholinergic drugs rescue synaptic plasticity in DYT1 dystonia: Role of M1 muscarinic receptors. Mov Disord. 2014;29:1655–65.CrossRefGoogle ScholarPubMed
Teo, JT, Edwards, MJ, Bhatia, K. Tardive dyskinesia is caused by maladaptive synaptic plasticity: a hypothesis. Mov Disord. 2012;27:1205–15.CrossRefGoogle ScholarPubMed

Suggested Readings

Breger, LS, Lane, EL. L-DOPA and graft-induced dyskinesia: different treatment, same story? Exp Biol Med (Maywood). 2013;238:725–32.CrossRefGoogle ScholarPubMed
Lane, EL, Winkler, C. L-DOPA- and graft-induced dyskinesia following transplantation. Prog Brain Res. 2012;200:143–68.CrossRefGoogle ScholarPubMed

Suggested Readings

Gras, D, Jonard, L, Roze, E, et al. Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene. J Neurol Neurosurg Psychiatry. 2012;83:956–62.CrossRefGoogle Scholar
Veneziano, L, Parkinson, MH, Mantuano, E, Frontali, M, Bhatia, KP, Giunti, P. A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literature. Cerebellum. 2014;13:588–95.CrossRefGoogle Scholar

Suggested Readings

Carapito, R, Paul, N, Untrau, M, et al. A De Novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystonia. Mov Disord. 2015;30:423–7.CrossRefGoogle Scholar
Chen, DH, Méneret, A, Friedman, JR., et al. ADCY5-related dyskinesia: broader spectrum and genotype-phenotype correlations. Neurology. 2015;85:2026–3.Google Scholar
Mencacci, NE, Erro, R, Wiethoff, S. et al. ADCY5 mutations are another cause of benign hereditary chorea. Neurology. 2015;85:80–8.CrossRefGoogle ScholarPubMed

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  • Chorea
  • Kailash P. Bhatia, Institute of Neurology, University College London, Roberto Erro, Maria Stamelou, University of Athens, Greece
  • Book: Case Studies in Movement Disorders
  • Online publication: 04 July 2017
  • Chapter DOI: https://doi.org/10.1017/9781316145050.034
Available formats
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Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

  • Chorea
  • Kailash P. Bhatia, Institute of Neurology, University College London, Roberto Erro, Maria Stamelou, University of Athens, Greece
  • Book: Case Studies in Movement Disorders
  • Online publication: 04 July 2017
  • Chapter DOI: https://doi.org/10.1017/9781316145050.034
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Chorea
  • Kailash P. Bhatia, Institute of Neurology, University College London, Roberto Erro, Maria Stamelou, University of Athens, Greece
  • Book: Case Studies in Movement Disorders
  • Online publication: 04 July 2017
  • Chapter DOI: https://doi.org/10.1017/9781316145050.034
Available formats
×