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Gelsolin Familial Amyloidosis Peripheral Neuropathy in Canada: A Case Report

  • Majed Alabdali (a1) (a2), Carolina Barnett (a1), Alon Abraham (a1), Danah Al Jaafari (a1) (a2) and Vera Bril (a1) (a3)...
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Abstract

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References

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1. Kiuru-Enari, S, Haltia, M. Hereditary gelsolin amyloidosis. Handb Clin Neurol. 2013;115:659-681.
2. Taira, M, Ishiura, H, Mitsui, J, Takahashi, Y, Hayashi, T, Shimizu, J, et al. Clinical features and haplotype analysis of newly identified Japanese patients with gelsolin-related familial amyloidosis of Finnish type. Neurogenetics. 2012;13:237-243.
3. Levy, E, Haltia, M, Fernandez-Madrid, I, Koivunen, O, Ghiso, J, Prelli, F, et al. Mutation in gelsolin gene in Finnish hereditary amyloidosis. J Exp Med. 1990;172:1865-1867.
4. Maury, CP, Liljeström, M, Boysen, G, Törnroth, T, la Chapelle de, A, Nurmiaho-Lassila, EL. Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type). J Clin Pathol. 2000;53:95-99.
5. Kiuru-Enari, S, Somer, H, Seppäläinen, A-M, Notkola, I-L, Haltia, M. Neuromuscular pathology in hereditary gelsolin amyloidosis. J Neuropathol Exp Neurol. 2002;61:565-571.
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Canadian Journal of Neurological Sciences
  • ISSN: 0317-1671
  • EISSN: 2057-0155
  • URL: /core/journals/canadian-journal-of-neurological-sciences
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