✦ LIBER ✦

Systemic vasodilation is a predominant cause of hypotension in a patient with familial amyloid polyneuropathy during liver transplantation

✍ Scribed by Gundappa Neelakanta; Aman Mahajan; Cynthia Antin

Book ID: 116621108
Publisher: Elsevier Science
Year: 2005
Tongue: English
Weight: 73 KB
Volume: 17
Category: Article
ISSN: 0952-8180
DOI: 10.1016/j.jclinane.2004.03.014

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Liver transplantation and combined liver

Liver transplantation and combined liver-heart transplantation in patients with familial amyloid polyneuropathy: A single-center experience

✍ Ana-Paula Barreiros; Felix Post; Maria Hoppe-Lotichius; Reinhold P. Linke; Chris 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 201 KB

Liver transplantation (LT) is the only curative option for patients with familial amyloid polyneuropathy (FAP) at present. Twenty patients with FAP underwent LT between May 1998 and June 2007. Transthyretin mutations included predominantly the Val30Met mutation but also 10 other mutations. Seven pat

Marked regression of abdominal fat amylo

Marked regression of abdominal fat amyloid in patients with familial amyloid polyneuropathy during long-term follow-up after liver transplantation

✍ Ayako Tsuchiya; Masahide Yazaki; Fuyuki Kametani; Yo-ichi Takei; Shu-ichi Ikeda 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 504 KB

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

2 Liver transplantation for familial amy

2 Liver transplantation for familial amyloid polyneuropathy does not prevent disease progression in a majority of patients

✍ Roman E. Perri; David Brandhagen; Steven Zeldenrust; Charles B. Rosen; John J. P 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 124 KB

Progression of cardiomyopathy and neurop

Progression of cardiomyopathy and neuropathy after liver transplantation in a patient with familial amyloidotic polyneuropathy caused by tyrosine-77 transthyretin variant

✍ García-Herola, Antonio ;Prieto, Martín ;Pascual, Sonia ;Berenguer, Marina ;López 📂 Article 📅 1999 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 34 KB

Familial amyloidotic polyneuropathy is an inherited form of amyloidosis associated with a mutant form of a protein called transthyretin. The Methionine-30 variant is the most frequent mutation observed. This disorder is caused by deposition of this protein as amyloid in several organs, such as the h

Liver transplantation in patients with f

Liver transplantation in patients with familial amyloidotic polyneuropathy (FAP) : study in a cohort of 29 patients and long-term results in 10 patients

✍ D. Adams; D. Samuel; C. Goulon-Goeau; PMP Costa; M. Nakazato; S. Metral; H. Bism 📂 Article 📅 1998 🏛 Elsevier Science 🌐 English ⚖ 182 KB