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Section 6 - Movement Disturbances

Published online by Cambridge University Press:  27 July 2023

Mark McCarron
Affiliation:
Ulster University
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55 Cases in Neurology
Case Histories and Patient Perspectives
, pp. 263 - 314
Publisher: Cambridge University Press
Print publication year: 2023

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References

References

Postuma, RB, Lang, AE. Hemiballism: revisiting a classic disorder. Lancet Neurol. 2003;2(11):661–8.Google ScholarPubMed
Compston, A. Hemichorea resulting from a local lesion of the brain. (The syndrome of the body of Luys.) By James Purdon Martin, MD (London). Brain 1927:50; 637–651; Hemichorea associated with a lesion of the corpus Luysii. By James Purdon Martin and N.S. Alcock. Brain. 1934:57; 504–516; and Hemichorea (hemiballismus) without lesions in the corpus Luysii. By J. Purdon Martin (From the National Hospital, Queen Square, W.C.1) Brain. 1957:80; 1–10. Brain. 2006;129(7):1633–6.Google Scholar
Chua, CB, Sun, CK, Hsu, CW et al. ‘Diabetic striatopathy’: clinical presentations, controversy, pathogenesis, treatments, and outcomes. Sci Rep. 2020;10(1):111.CrossRefGoogle ScholarPubMed

References

Spasovski, G, Vanholder, R, Allolio, B et al. Clinical practice guideline on diagnosis and treatment of hyponatraemia. Eur J Endocrinol. 2014;170(3):G147.CrossRefGoogle ScholarPubMed
Fox, B. Crash diet potomania. Lancet. 2002;359:942.CrossRefGoogle ScholarPubMed
Adams, RD, Victor, M, Mancall, EL. Central pontine myelinolysis: a hitherto undescribed disease occurring in alcoholic and malnourished patients. AMA Arch Neurol Psychiatry. 1959;81(2):154–72.Google ScholarPubMed

References

Zwergal, A, Dieterich, M. Vertigo and dizziness in the emergency room. Curr Opin Neurol. 2020;33(1):117–25.CrossRefGoogle ScholarPubMed
Krishnan, K, Bassilious, K, Eriksen, E et al. Posterior circulation stroke diagnosis using HINTS in patients presenting with acute vestibular syndrome: a systematic review. Eur stroke J. 2019;4(3):233–9.CrossRefGoogle ScholarPubMed
Edlow, JA, Gurley, KL, Newman-Toker, DE. A new diagnostic approach to the adult patient with acute dizziness. J Emerg Med. 2018;54(4):469–83.CrossRefGoogle Scholar
Matsumoto, J, Ogata, T, Abe, H et al. Do characteristics of dissection differ between the posterior inferior cerebellar artery and the vertebral artery? J Stroke Cerebrovasc Dis. 2014;23(10):2857–61.CrossRefGoogle ScholarPubMed

References

Giunti, P, Mantuano, E, Frontali, M, Veneziano, L. Molecular mechanism of spinocerebellar ataxia type 6: glutamine repeat disorder, channelopathy and transcriptional dysregulation. The multifaceted aspects of a single mutation. Front Cell Neurosci. 2015;9:5.CrossRefGoogle ScholarPubMed
Müller, U. Spinocerebellar ataxias (SCAs) caused by common mutations. Neurogenetics. 2021;22(4):235–50.CrossRefGoogle ScholarPubMed
Jacobi, H, du Montcel, ST, Bauer, P et al. Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study. Lancet Neurol. 2015;14(11):1101–8.CrossRefGoogle ScholarPubMed

References

Pousset, F, Legrand, L, Monin, M-L et al. A 22-year follow-up study of long-term cardiac outcome and predictors of survival in Friedreich ataxia. JAMA Neurol. 2015 Nov.;72(11):1334–41.CrossRefGoogle ScholarPubMed
Campuzano, V, Montermini, L, Moltò, MD et al. Friedreich’s ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science. 1996 Mar.;271(5254):1423–7.CrossRefGoogle ScholarPubMed
Dürr, A, Cossee, M, Agid, Y et al. Clinical and genetic abnormalities in patients with Friedreich’s ataxia. N Engl J Med. 1996 Oct.;335(16):1169–75.CrossRefGoogle ScholarPubMed
Gwathmey, KG. Sensory neuronopathies. Muscle Nerve. 2016;53:819.CrossRefGoogle ScholarPubMed
Amato, AA, Ropper, AH. Sensory ganglionopathy. N Engl J Med. 2020;383;1657–62.CrossRefGoogle ScholarPubMed
Fargeot, G, Echaniz-Laguna, A. Sensory neuronopathies: new genes, new antibodies and new concepts. J Neurol Neurosurg & Psychiatry. 2021;92:398406.CrossRefGoogle Scholar

References

Bloem, BR, Okun, MS, Klein, C. Parkinson’s disease. Lancet. 2021;397(10291):2284–303.CrossRefGoogle ScholarPubMed
Postuma, RB, Berg, D, Stern, M et al. MDS clinical diagnostic criteria for Parkinson’s disease. Mov Disord. 2015;30(12):1591–601.CrossRefGoogle ScholarPubMed
Ali, K, Morris, HR. Parkinson’s disease: chameleons and mimics. Pract Neurol. 2015;15(1):1425.CrossRefGoogle ScholarPubMed

References

Berger, JR, Aksamit, AJ, Clifford, DB et al. PML diagnostic criteria: consensus statement from the AAN neuroinfectious disease section. Neurology. 2013;80(15):1430–8.CrossRefGoogle ScholarPubMed
Major, EO, Yousry, TA, Clifford, DB. Pathogenesis of progressive multifocal leukoencephalopathy and risks associated with treatments for multiple sclerosis: a decade of lessons learned. Lancet Neurol. 2018;17(5):467–80.CrossRefGoogle ScholarPubMed
Henegar, CE, Eudy, AM, Kharat, V et al. Progressive multifocal leukoencephalopathy in patients with systemic lupus erythematosus: a systematic literature review. Lupus. 2016;25(6):617–26.CrossRefGoogle ScholarPubMed

References

de Silva, RN, Vallortigara, J, Greenfield, J et al. Diagnosis and management of progressive ataxia in adults. Pract Neurol. 2019;19(3):196207.CrossRefGoogle ScholarPubMed
Németh, AH, Kwasniewska, AC, Lise, S et al. Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model. Brain. 2013;136(10):3106–18.CrossRefGoogle ScholarPubMed
de Silva, R, Greenfield, J, Cook, A et al. Guidelines on the diagnosis and management of the progressive ataxias. Orphanet J Rare Dis. 2019;14:51.CrossRefGoogle ScholarPubMed
Vermeer, S, Hoischen, A, Meijer, RPP et al. Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia. Am J Hum Genet. 2010;87(6):813–9.CrossRefGoogle ScholarPubMed
Beaudin, M, Matilla-Dueñas, A, Soong, B-W et al. The classification of autosomal recessive cerebellar ataxias: a consensus statement from the society for research on the cerebellum and ataxias task force. Cerebellum 2019;18(6):1098–125.CrossRefGoogle Scholar

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