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Review Article

Gelsolin amyloidosis: genetics, biochemistry, pathology and possible strategies for therapeutic intervention

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Pages 282-296 | Received 17 Oct 2011, Accepted 24 Jan 2012, Published online: 24 Feb 2012

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Per Hammarström & Sofie Nyström. (2023) Viruses and amyloids - a vicious liaison. Prion 17:1, pages 82-104.
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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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Rosanna Dammacco, Giampaolo Merlini, Walter Lisch, Tero T. Kivelä, Ermete Giancipoli, Angelo Vacca & Franco Dammacco. (2020) Amyloidosis and Ocular Involvement: an Overview. Seminars in Ophthalmology 35:1, pages 7-26.
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Francesco Bonì, Mario Milani, Eloise Mastrangelo, Alberto Babiroli, Luisa Diomede & Matteo de Rosa. (2019) An alternative non-proteolytic mechanism may underlie AGel amyloidosis. Amyloid 26:sup1, pages 150-151.
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Tiia Pihlamaa, Sinikka Suominen, Sari Kiuru-Enari & Maarit Tanskanen. (2016) Increasing amount of amyloid are associated with the severity of clinical features in hereditary gelsolin (AGel) amyloidosis. Amyloid 23:4, pages 225-233.
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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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Sari Atula, Tuuli Nikoskinen, Aleksi Saastamoinen, Daniel Strbian, Eeva-Kaisa Schmidt & Sari Kiuru-Enari. (2016) Gender differences in the clinical course of Finnish gelsolin amyloidosis. Amyloid 23:1, pages 33-38.
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Tuuli Nikoskinen, Eeva-Kaisa Schmidt, Daniel Strbian, Sari Kiuru-Enari & Sari Atula. (2015) Natural course of Finnish gelsolin amyloidosis. Annals of Medicine 47:6, pages 506-511.
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Yvonne A. Efebera, Amy Sturm, Elizabeth C. Baack, Craig C. Hofmeister, Anjali Satoskar, Tibor Nadasdy, Gyongyi Nadasdy, Don M. Benson, Julian D. Gillmore, Philip N. Hawkins & Dorota Rowczenio. (2014) Novel gelsolin variant as the cause of nephrotic syndrome and renal amyloidosis in a large kindred. Amyloid 21:2, pages 110-112.
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Pirjo Juusela, Maarit Tanskanen, Anja Nieminen, Kirsti Kari, Liisa Suominen, Veli-Jukka Uitto & Sari Kiuru-Enari. (2013) Xerostomia in hereditary gelsolin amyloidosis. Amyloid 20:1, pages 39-44.
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