Diagnostic value of abdominal fat tissue aspirate in familial amyloid polyneuropathy
β Scribed by Keiko Maruyama; Shu-ichi Ikeda; Nobuo Yanagisawa; Masamitsu Nakazato
- Book ID
- 118930399
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 654 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0022-510X
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To elucidate whether the amount of tissue-deposited amyloid in familial amyloid polyneuropathy (FAP) patients decreases or increases over the long-term course after liver transplantation (LT), we examined changes in histopathological and biochemical characteristics of abdominal fat amyloid in the tr
## Abstract Amyloidosis is a heterogeneous group of diseases with a common outcome: deposition of insoluble protein in the visceral organs and tissues. Primary amyloidosis is a consequence of different plasma cell disorders, and it is the most common form of amyloidosis in the United States with an