Extended Phenotype in the Transthyretin Tyr77 Familial Amyloid Polyneuropathy-Reference-Cited by-同舟云学术

Extended Phenotype in the Transthyretin Tyr77 Familial Amyloid Polyneuropathy

Published:2005 Issue:2 Volume:53 Page:55-59
ISSN:0014-3022
Container-title:European Neurology
language:en
Short-container-title:Eur Neurol

Author:

Lossos Alexander,Soffer Dov,Steiner-Birmanns Bettina,Hassin-Baer Sharon,Sadeh Menachem,Sagi Michal,Linetski Eduard,Abramsky Oded,Argov Zohar,Rosenmann Hanna

Publisher

S. Karger AG

Subject

Clinical Neurology,Neurology

Reference29 articles.

1. Transthyretin-associated neuropathic amyloidosis: Pathogenesis and treatment

2. Transthyretin mutations in hyperthyroxinemia and amyloid diseases

3. Massive leptomeningeal amyloidosis associated with a Val30Met transthyretin gene

4. Familial Amyloidosis: A Study of 52 North American-Born Patients Examined During a 30-Year Period

5. Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77)

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features;Annals of Clinical and Translational Neurology;2023-02-11

2. Conjunctival lymphangiectasia as a biomarker of severe systemic disease in Ser77Tyr hereditary transthyretin amyloidosis;British Journal of Ophthalmology;2020-01-16

3. Association between hearing loss and hereditary ATTR amyloidosis;Amyloid;2019-09-10

4. How your ears can tell what is hidden in your heart: wild-type transthyretin amyloidosis as potential cause of sensorineural hearing loss inelderly-AmyloDEAFNESS pilot study;Amyloid;2017-04-03

5. Hereditary Transthyretin Amyloidosis in Eight Chinese Families;Chinese Medical Journal;2015-11-05