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Amyloid
The Journal of Protein Folding Disorders
Volume 22, 2015 - Issue 3
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Letter to the Editor

Effects of liver transplantation and tafamidis in hereditary transthyretin amyloidosis caused by transthyretin Leu55Pro mutation: a case report

Tomoya KonDepartment of Neurology, Aomori Prefectural Central Hospital, Aomori, Japan, Correspondence[email protected]
,
Yohei MisumiDepartment of Neurology,
,
Haruo NishijimaDepartment of Neurology, Aomori Prefectural Central Hospital, Aomori, Japan,
,
Masaki HondaDepartment of Pediatric Surgery and Transplantation, Graduate School of Medical Sciences, and
,
Chieko SuzukiDepartment of Neurology, Aomori Prefectural Central Hospital, Aomori, Japan,
,
Masayuki BabaDepartment of Neurology, Aomori Prefectural Central Hospital, Aomori, Japan,
,
Yukihiro InomataDepartment of Pediatric Surgery and Transplantation, Graduate School of Medical Sciences, and
,
Konen ObayashiDepartment of Morphological and Physiological Sciences, Graduate School of Health Sciences, Kumamoto University, Kumamoto, Japan
,
Yukio AndoDepartment of Neurology,
&
Masahiko TomiyamaDepartment of Neurology, Aomori Prefectural Central Hospital, Aomori, Japan,
show all
Pages 203-204 | Received 04 Mar 2015, Accepted 16 Mar 2015, Published online: 30 Jun 2015

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Toshiya Nomura, Taro Yamashita, Yohei Misumi, Mitsuharu Ueda, Teruaki Masuda, Masayoshi Tasaki & Yukio Ando. (2017) A case with a novel variant transthyretin A36D presenting cardiac phenotype. Amyloid 24:sup1, pages 100-100.
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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 (7)

Huayuan Yuan, Ya Lin, Jiao Wang, Jialian Li, Xuefeng Chen, Yulong Guo & Jiong Tang. (2023) Hypertrophic cardiomyopathy caused by a heterozygous variant in TTR gene: A case report. Medicine 102:20, pages e33752.
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Daniela Grasso, Silvia Galderisi, Annalisa Santucci & Andrea Bernini. (2023) Pharmacological Chaperones and Protein Conformational Diseases: Approaches of Computational Structural Biology. International Journal of Molecular Sciences 24:6, pages 5819.
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Sadao Hikishima, Kenji Sakai, Akio Akagi, Hiroki Yamaguchi, Shutaro Shibata, Koji Hayashi, Hiroto Nakano, Mizuki Kanemoto, Yuta Usui, Yu Taniguchi, Junji Komatsu, Keiko Nakamura-Shindo, Ichiro Nozaki, Tsuyoshi Hamaguchi, Kenjiro Ono, Kazuo Iwasa & Masahito Yamada. (2022) Deterioration after Liver Transplantation and Transthyretin Stabilizer Administration in a Patient with ATTRv Amyloidosis with a Leu58Arg (p.Leu78Arg) <i>TTR</i> Variant. Internal Medicine 61:15, pages 2347-2351.
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Monica Alcantara, Michelle M. Mezei, Steven K. Baker, Ari Breiner, Priya Dhawan, Amanda Fiander, Nowell M. Fine, Christopher Hahn, Hans D. Katzberg, Shahin Khayambashi, Rami Massie, Genevieve Matte, Brendan Putko, Zaeem Siddiqi, Diego Delgado & Vera Bril. (2021) Canadian Guidelines for Hereditary Transthyretin Amyloidosis Polyneuropathy Management. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 49:1, pages 7-18.
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Matthew J. Jennings, Angela Lochmüller, Antonio Atalaia & Rita Horvath. (2021) Targeted Therapies for Hereditary Peripheral Neuropathies: Systematic Review and Steps Towards a ‘treatabolome’. Journal of Neuromuscular Diseases 8:3, pages 383-400.
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Jing Xu, Meng Yang, Xiaoxia Pan, Xialian Yu, Jingyuan Xie, Hong Ren, Xiao Li & Nan Chen. (2017) Transthyretin-related hereditary amyloidosis with recurrent vomiting and renal insufficiency as the initial presentation. Medicine 96:10, pages e5737.
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Leslie Matalonga, Laura Gort & Antonia Ribes. (2016) Small molecules as therapeutic agents for inborn errors of metabolism. Journal of Inherited Metabolic Disease 40:2, pages 177-193.
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