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18 - Asim K. Bag, Victor Hugo Rocha Marussi, Lázaro Luís Faria do Amaral

from Part I - Neurodegenerative Diseases

Published online by Cambridge University Press:  06 January 2017

Lázaro Luís Faria do Amaral
Affiliation:
Hospital Beneficência Portuguesa
Asim K. Bag
Affiliation:
University of Alabama, Birmingham
Fabrício Guimarães Gonçalves
Affiliation:
University of Brazil
Prasad B. Hanagandi
Affiliation:
University of Toronto
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Summary

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Chapter
Information
Advanced Neuroradiology Cases
Challenge Your Knowledge
, pp. 59 - 62
Publisher: Cambridge University Press
Print publication year: 2016

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References

Josephs, KA, Whitwell, JL, Parisi, JE, et al. Caudate atrophy on MRI is a characteristic feature of FTLD-FUS. Eur J Neurol 2010; 17(7): 969–75.Google Scholar
Karageorgiou, E, Miller, BL. Frontotemporal lobar degeneration: a clinical approach. Semin Neurol 2014; 34(2): 189–201.Google Scholar
Rohrer, JD, Lashley, T, Schott, JM, et al. Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration. Brain 2011; 134(Pt 9): 2565–81.Google Scholar
Seelaar, H, Klijnsma, KY, Koning, I de, et al. Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration. J Neurol 2010; 257(5): 747–53.Google Scholar
Siuda, J, Lewicka, T, Bujak, M, et al. ALS-FTD complex disorder due to C9ORF72 gene mutation: description of first Polish family. Eur Neurol 2014; 72(1-2): 64–71.Google Scholar
Blitterswijk, M van, DeJesus-Hernandez, M, Niemantsverdriet, E, et al. Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study. Lancet Neurol 2013; 12(10): 978–88.Google Scholar

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