๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

A case of late onset cardiac amyloidosis with a new transthyretin variant (Lysine 92)

โœ Scribed by Fumio Saito; Masamitsu Nakazato; Haruhiko Akiyama; Yasuyuki Kitahara; Yukari Date; Yoshikazu Iwasaki; Shinsuke Harasawa; Ryouhei Hisaki; Toshiyuki Horie; Noriko Kinukawa; Takayoshi Watanabe; Tatsuo Sakamaki; Hiroshi Yagi; Yoshinobu Hoshii; Chikao Yutani; Katsuo Kanmatsuse


Book ID
117818376
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
158 KB
Volume
32
Category
Article
ISSN
1532-8392

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Transthyretin Pro55, a variant associate
โœ Daniel R. Jacobson; Dale E. McFarlin; Immaculata Kane; Joel N. Buxbaum ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› Springer ๐ŸŒ English โš– 349 KB

Mutations in the protein transthyretin cause amyloidosis involving the heart, peripheral nerves, and other organs. A family from West Virginia developed an unusually aggressive form of widespread transthyretin amyloidosis. Single-strand conformation polymorphism analysis revealed a variant in the tr

Hereditary amyloidosis: description of a
โœ Merrill D. Benson; Margaret R. Wallace; Eduardo Tejada; Hal Baumann; Burnestine ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 766 KB

A family with hereditary amyloidosis characterized by peripheral neuropathy and cardiomyopathy is described. Lack of eye involvement sets their disease apart from the Indiana/Swiss familial amyloidotic polyneuropathy type 11. The disease is of late onset; affected members die of cardiomyopathy after