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Amyloid
The Journal of Protein Folding Disorders
Volume 22, 2015 - Issue 4
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Letter to the Editor

Two brothers homozygous for the TTR V30M both presenting with a phenotype dominated by central nervous complications

Yuto UchidaDepartment of Neurology, Toyokawa City Hospital, 23 Noji, Yawata-cho, Toyokawa 442-8561, Aichi, Japan, Correspondence[email protected]
,
Koji TakadaDepartment of Neurology, Toyokawa City Hospital, 23 Noji, Yawata-cho, Toyokawa 442-8561, Aichi, Japan,
,
Yasukuni TsuguDepartment of Neurology, Toyokawa City Hospital, 23 Noji, Yawata-cho, Toyokawa 442-8561, Aichi, Japan,
,
Mitsuharu UedaDepartment of Neurology, Kumamoto University, Kumamoto, Japan,
,
Taro YamashitaDepartment of Neurology, Kumamoto University, Kumamoto, Japan,
,
Yukio AndoDepartment of Neurology, Kumamoto University, Kumamoto, Japan,
,
Susumu KobayashiDepartment of Radiology, Toyokawa City Hospital, Aichi, Japan,
,
Haruki KoikeDepartment of Neurology, Nagoya University, Aichi, Japan,
,
Takayuki WatanabeDepartment of Neurosurgery, Toyokawa City Hospital, Aichi, Japan, and
,
Takashi MatsumotoDepartment of Neurosurgery, Toyokawa City Hospital, Aichi, Japan, and
,
Takanari ToyodaDepartment of Neurology, Nagoya City University, Aichi, Japan
,
Gohei YamadaDepartment of Neurology, Nagoya City University, Aichi, Japan
&
Noriyuki MatsukawaDepartment of Neurology, Nagoya City University, Aichi, Japan
 show all
Pages 261-262 | Received 24 Aug 2015, Accepted 04 Oct 2015, Published online: 20 Nov 2015

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Taro Yamashita, Mitsuharu Ueda, Nobuyuki Saga, Kiyonori Nanto, Masayoshi Tasaki, Teruaki Masuda, Yohei Misumi, Seitaro Oda, Akiko Fujimoto, Tomoko Amano, Kotaro Takamatsu, Satoshi Yamashita, Konen Obayashi, Hirotaka Matsui & Yukio Ando. (2016) Hereditary amyloidosis with cardiomyopathy caused by the novel variant transthyretin A36D. Amyloid 23:3, pages 207-208.
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Articles from other publishers (2)

Xujun Chu, Mengdie Wang, Ran Tang, Yanan Huang, Jiaxi Yu, Yunfeng Cao, Yilei Zheng, Zhiying Xie, Jianwen Deng, Zhi Wang, Wei Ma, Wenjing Song, Yuan Wu, He Lv, Wei Zhang, Zhaoxia Wang, Yun Yuan, Yu Liu & Lingchao Meng. (2022) Clinical and biochemical characterization of hereditary transthyretin amyloidosis caused by E61K mutation. Frontiers in Molecular Neuroscience 15.
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Yuta Maetani, Dai Agari, Eiichi Nomura, Mitsuharu Ueda, Yukio Ando & Takemori Yamawaki. (2016) Familial amyloid polyneuropathy involving a homozygous Val30Met mutation in the amyloidogenic transthyretin gene presenting with superficial siderosis: a case report. Rinsho Shinkeigaku 56:6, pages 430-434.
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