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Amyloid
The Journal of Protein Folding Disorders
Volume 23, 2016 - Issue 4
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Original Article

Increasing amount of amyloid are associated with the severity of clinical features in hereditary gelsolin (AGel) amyloidosis

Tiia PihlamaaDepartment of Plastic and Reconstructive Surgery, Helsinki University Hospital, Helsinki, Finland, Correspondence[email protected]
,
Sinikka SuominenDepartment of Plastic and Reconstructive Surgery, Helsinki University Hospital, Helsinki, Finland,
,
Sari Kiuru-EnariDepartment of Neurology, Clinical Neurosciences, University of Helsinki, Helsinki, Finland, and
&
Maarit TanskanenDepartment of Pathology, University of Helsinki and HUSLAB, Helsinki, Finland
Pages 225-233 | Received 01 Jun 2016, Accepted 15 Sep 2016, Published online: 23 Nov 2016

Citations (5)

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Read on this site (1)

Eeva-Kaisa Schmidt, Sari Kiuru-Enari, Sari Atula & Maarit Tanskanen. (2019) Amyloid in parenchymal organs in gelsolin (AGel) amyloidosis. Amyloid 26:3, pages 118-124.
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Articles from other publishers (4)

Rong Zhang, Fangfang Shang, Danyang Li, Yuan Zhang & Li Yuan. (2021) The first Chinese renal gelsolin amyloidosis with the p.Asp174Asn mutation in the GSN gene: Nephrology picture. Journal of Nephrology 34:4, pages 1257-1259.
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Michela Bollati, Luisa Diomede, Toni Giorgino, Carmina Natale, Elisa Fagnani, Irene Boniardi, Alberto Barbiroli, Rebecca Alemani, Marten Beeg, Marco Gobbi, Ana Fakin, Eloise Mastrangelo, Mario Milani, Gianluca Presciuttini, Edi Gabellieri, Patrizia Cioni & Matteo de Rosa. (2021) A novel hotspot of gelsolin instability triggers an alternative mechanism of amyloid aggregation. Computational and Structural Biotechnology Journal 19, pages 6355-6365.
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Eeva-Kaisa Schmidt, Tuuli Mustonen, Sari Kiuru-Enari, Tero T. Kivelä & Sari Atula. (2020) Finnish gelsolin amyloidosis causes significant disease burden but does not affect survival: FIN-GAR phase II study. Orphanet Journal of Rare Diseases 15:1.
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Tuuli Mustonen, Eeva-Kaisa Schmidt, Miko Valori, Pentti J Tienari, Sari Atula & Sari Kiuru-Enari. (2017) Common origin of the gelsolin gene variant in 62 Finnish AGel amyloidosis families. European Journal of Human Genetics 26:1, pages 117-123.
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