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  • Print publication year: 2017
  • Online publication date: July 2017

26 - Dystonia Complicated by Pyramidal Signs, Parkinsonism, and Cognitive Impairment: HSP11

from Section 2 - Dystonia
Abdel Aleem, A, Abu-Shahba, N, Swistun, D, et al. Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosum. Eur J Med Genet. 2011;54:82–5.
Paisán-Ruiz, C, Guevara, R, Federoff, M, et al. Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations. Mov Disord. 2010;25:1791–800.
Schneider, SA, Mummery, CJ, Mehrabian, M, Houlden, H, Bain, PG. SPG11 presenting with tremor. Tremor Other Hyperkinet Mov (N Y). 2012;2. pii: tre-02-104-666-1.