In patients with familial amyloidotic polyneuropathy (FAP), heart complications are prognostic factors for mortality and morbidity after liver transplantation (LT). However, only a few studies have analyzed the development of arrhythmia in transplant patients with FAP. We investigated the developmen
β¦ LIBER β¦
Effect of albumin on transthyretin and amyloidogenic transthyretin Val30Met disposition and tissue deposition in familial amyloidotic polyneuropathy
β Scribed by Taguchi, Kazuaki; Jono, Hirofumi; Kugimiya-Taguchi, Tomoe; Nagao, Saori; Su, Yu; Yamasaki, Keishi; Mizuguchi, Mineyuki; Maruyama, Toru; Ando, Yukio; Otagiri, Masaki
- Book ID
- 122310826
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 678 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0024-3205
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Familial amyloid polyneuropathy (FAP) is a form of hereditary generalized amyloidosis. Liver tissue explanted from FAP patients has normal structure and function, except for the production of amyloidogenic variant transthyretin (TTR), and domino liver transplantation (DLT) using grafts from FAP pati