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Amyloid
The Journal of Protein Folding Disorders
Volume 5, 1998 - Issue 1
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Review Article

Gelsolin-related familial amyloidosis, Finnish type (FAF), and its variants found worldwide

Sari Kiuru Department of Neurology, University of Helsinki, Helsinki, Finland
Pages 55-66 | Received 14 Jul 1997, Accepted 18 Sep 1997, Published online: 06 Jul 2009

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Lisa Mendelson, Tatiana Prokaeva, K. H. Vincent Lau, Vaishali Sanchorawala, Kristen McCausland, Brian Spencer, Surendra Dasari, Ellen D. McPhail & Michelle C. Kaku. (2023) Hereditary gelsolin amyloidosis: a rare cause of cranial, peripheral and autonomic neuropathies linked to D187N and Y447H substitutions. Amyloid 30:4, pages 357-363.
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Susanna Koskelainen, Fang Zhao, Hannu Kalimo, Marc Baumann & Sari Kiuru-Enari. (2020) Severe elastolysis in hereditary gelsolin (AGel) amyloidosis. Amyloid 27:2, pages 81-88.
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Eeva-Kaisa Schmidt, Sari Atula, Maarit Tanskanen, Tuuli Nikoskinen, Irma-Leena Notkola & Sari Kiuru-Enari. (2016) Causes of death and life span in Finnish gelsolin amyloidosis. Annals of Medicine 48:5, pages 352-358.
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Dorota Rowczenio, Glenys A. Tennent, Janet Gilbertson, Helen J. Lachmann, David F. Hutt, Alison Bybee, Philip N. Hawkins & Julian D. Gillmore. (2014) Clinical characteristics and SAP scintigraphic findings in 10 patients with AGel amyloidosis. Amyloid 21:4, pages 276-281.
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Tiia Pihlamaa, Sinikka Suominen & Sari Kiuru-Enari. (2012) Familial amyloidotic polyneuropathy type IV – gelsolin amyloidosis. Amyloid 19:sup1, pages 30-33.
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James P. Solomon, Lesley J. Page, William E. Balch & Jeffery W. Kelly. (2012) Gelsolin amyloidosis: genetics, biochemistry, pathology and possible strategies for therapeutic intervention. Critical Reviews in Biochemistry and Molecular Biology 47:3, pages 282-296.
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Kouki Makioka, Masaki Ikeda, Yoshio Ikeda, Ai Nakasone, Tenshi Osawa, Atsushi Sasaki, Tomohiro Otani, Masashi Arai & Koichi Okamoto. (2010) Familial amyloid polyneuropathy (Finnish type) presenting multiple cranial nerve deficits with carpal tunnel syndrome and orthostatic hypotension. Neurological Research 32:5, pages 472-475.
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Maarit Tanskanen, Anders Paetau, Oili Salonen, Tapani Salmi, Antti Lamminen, Perttu Lindsberg, Hannu Somer & Sari Kiuru-Enari. (2009) Withdrawn: Severe ataxia with neuropathy in hereditary gelsolin amyloidosis. Amyloid 16:4, pages 246-246.
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M. Teresa Pastor, Alexandra Esteras-Chopo & Luis Serrano. (2007) Hacking the Code of Amyloid Formation. Prion 1:1, pages 9-14.
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Maarit Tanskanen, Anders Paetau, Oili Salonen, Tapani Salmi, Antti Lamminen, Perttu Lindsberg, Hannu Somer & Sari Kiuru-Enari. (2007) Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: A case report. Amyloid 14:1, pages 89-95.
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Gibril O. Fadika & Marc Baumann. (2002) Peptides corresponding to gelsolin derived amyloid of the Finnish type (AGelFIN) adopt two distinct forms in solution of which only one can polymerize into amyloid fibrils and form complexes with apoE. Amyloid 9:2, pages 75-82.
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