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Amyloid
The Journal of Protein Folding Disorders
Volume 3, 1996 - Issue 2
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Original Article

Postmortem pathological findings in a Japanese patient with familial amyloidosis, Finnish type (FAF)

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Pages 134-139 | Received 28 Jun 1995, Accepted 16 Jan 1996, Published online: 06 Jul 2009

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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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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 (2009) Withdrawn: Severe ataxia with neuropathy in hereditary gelsolin amyloidosis.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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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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C.P.J. Maury, E.L. Nurmiaho-Lassila, G. Boysen & M. Liljeström. (2003) Fibrillogenesis in gelsolin-related familial amyloidosis. Amyloid 10:sup1, pages 21-25.
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Articles from other publishers (10)

Gargi Banerjee, John Collinge, Nick C Fox, Tammaryn Lashley, Simon Mead, Jonathan M Schott, David J Werring & Natalie S Ryan. (2023) Clinical considerations in early-onset cerebral amyloid angiopathy. Brain.
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Tuuli Mustonen, Ville Sivonen, Sari Atula, Sari Kiuru-Enari & Saku T. Sinkkonen. (2021) Hearing problems in patients with hereditary gelsolin amyloidosis. Orphanet Journal of Rare Diseases 16:1.
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E-Nae Cheong, Wooyul Paik, Young-Chul Choi, Young-Min Lim, Hyunjin Kim, Woo Hyun Shim & Hyung Jun Park. (2021) Clinical Features and Brain MRI Findings in Korean Patients with AGel Amyloidosis. Yonsei Medical Journal 62:5, pages 431.
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S. Yamanaka, Y. Miyazaki, K. Kasai, S.-i. Ikeda, S. Kiuru-Enari & T. Hosoya. (2013) Hereditary renal amyloidosis caused by a heterozygous G654A gelsolin mutation: a report of two cases. Clinical Kidney Journal 6:2, pages 189-193.
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Sari Kiuru-Enari & Matti Haltia. 2013. Peripheral Nerve Disorders. Peripheral Nerve Disorders 659 681 .
Makiko Taira, Hiroyuki Ishiura, Jun Mitsui, Yuji Takahashi, Toshihiro Hayashi, Jun Shimizu, Takashi Matsukawa, Naoko Saito, Kazumasa Okada, Sadatoshi Tsuji, Hiromasa Sawamura, Shiro Amano, Jun Goto & Shoji Tsuji. (2012) Clinical features and haplotype analysis of newly identified Japanese patients with gelsolin-related familial amyloidosis of Finnish type. neurogenetics 13:3, pages 237-243.
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Isabel Conceição, Maria Lurdes Sales‐Luis, Mamede De Carvalho, Teresinha Evangelista, Rui Fernandes, Tiina Paunio, Hannele Kangas, Paula Coutinho, Carlos Neves & Maria João Saraiva. (2003) Gelsolin‐related familial amyloidosis, Finnish type, in a Portuguese family: Clinical and neurophysiological studies. Muscle & Nerve 28:6, pages 715-721.
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Sari Kiuru-Enari, Hannu Somer, Anna-Maria Seppäläinen, Irma-Leena Notkola & Matti Haltia. (2002) Neuromuscular Pathology in Hereditary Gelsolin Amyloidosis. Journal of Neuropathology & Experimental Neurology 61:6, pages 565-571.
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Tiina Paunio, Hannele Kangas, Outi Heinonen, Marie-Hélène Buc-Caron, Jean-Jacques Robert, Susanna Kaasinen, Ilkka Julkunen, Jacques Mallet & Leena Peltonen. (1998) Cells of the Neuronal Lineage Play a Major Role in the Generation of Amyloid Precursor Fragments in Gelsolin-related Amyloidosis. Journal of Biological Chemistry 273:26, pages 16319-16324.
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Tiina Paunio, Hannele Kangas, Sari Kiuru, Jorma Palo, Leena Peltonen & Ann-Christine Syvänen. (1997) Tissue distribution and levels of gelsolin mRNA in normal individuals and patients with gelsolin-related amyloidosis. FEBS Letters 406:1-2, pages 49-55.
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