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Amyloid
The Journal of Protein Folding Disorders
Volume 26, 2019 - Issue 4
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Letters to the Editor

A case of cerebral amyloid angiopathy-type hereditary ATTR amyloidosis with Y69H (p.Y89H) variant displaying transient focal neurological episodes as the main symptom

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Pages 251-252 | Received 19 Mar 2019, Accepted 13 Jun 2019, Published online: 01 Jul 2019

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Yusuke Takahashi, Kazuhiro Oguchi, Yusuke Mochizuki, Ken Takasone, Naoki Ezawa, Akira Matsushima, Nagaaki Katoh, Masahide Yazaki & Yoshiki Sekijima. (2023) Distribution and progression of cerebral amyloid angiopathy in early-onset V30M (p.V50M) hereditary ATTR amyloidosis. Amyloid 30:1, pages 109-118.
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Yusuke Takahashi, Nobuhiko Ohashi, Ken Takasone, Tsuneaki Yoshinaga, Masahide Yazaki, Michael Roberts, Paul F. Glidden & Yoshiki Sekijima. (2022) CSF/plasma levels, transthyretin stabilisation and safety of multiple doses of tolcapone in subjects with hereditary ATTR amyloidosis. Amyloid 29:3, pages 190-196.
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Articles from other publishers (2)

Natsumi Saito, Yasuko Kuroha, Arika Hasegawa, Mari Tada, Akiyoshi Kakita, Kei Watanabe & Tetsuya Takahashi. (2023) Case of hereditary Y69H (p.Y89H) transthyretin variant leptomeningeal amyloidosis presenting with drop attacks and recurrent transient language disorder転倒発作と反復する一過性の言語障害を呈したY69H (p.Y89H)変異型遺伝性トランスサイレチン髄膜アミロイドーシスの1例. Rinsho Shinkeigaku 63:10, pages 650-655.
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Erica Irene Uneus, Christer Wilhelmsson, David Bäckström, Intissar Anan, Jonas Wixner, Björn Pilebro, Katrine Riklund, Mattias Ögren, Margareta Ögreen, Jan Axelsson, Ole B. Suhr & Torbjörn Sundström. (2022) Cerebellar and Cerebral Amyloid Visualized by [18F]flutemetamol PET in Long-Term Hereditary V30M (p.V50M) Transthyretin Amyloidosis Survivors. Frontiers in Neurology 13.
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