Amyloid polyneuropathy caused by wild-type transthyretin-Reference-Cited by-同舟云学术

Amyloid polyneuropathy caused by wild-type transthyretin

Published:2015-03-14 Issue:1 Volume:52 Page:146-149
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Lam Lynda¹,Margeta Marta²,Layzer Robert³

Affiliation:

1. Department of Neurology; Kaiser Permanente Medical Center; San Rafael California USA

2. Department of Pathology; University of California; San Francisco California USA

3. Department of Neurology; University of California; San Francisco California USA

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.24563/fullpdf

Reference22 articles.

1. THAOS - The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis;Coelho;Curr Med Res Opin,2013

2. Senile systemic amyloidosis presenting with heart failure. A comparison with light chain-associated amyloidosis;Ng;Arch Intern Med,2005

3. Amyloid neuropathies;Shin;Mt Sinai J Med,2012

4. Sekijima Y Yoshida K Tokuda T Bird TD Dolan CR Fong CT Pagon RA Adam MP Ardinger HH Bird TD Dolan CR Fong CT GeneReviews® [Internet] Seattle, WA University of Washington, Seattle 1993 2014 http://www.ncbi.nlm.nih.gov/books/NBK1194/

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1. Distinctive Deposition Patterns of Sporadic Transthyretin-Derived Amyloidosis in the Atria: A Forensic Autopsy-Based Study;International Journal of Molecular Sciences;2024-07-26

2. Neurological affection and serum neurofilament light chain in wild type transthyretin amyloidosis;Scientific Reports;2024-05-02

3. Same same, but different? The neurological presentation of wildtype transthyretin (ATTRwt) amyloidosis;Amyloid;2022-01-07

4. Wild type transthyretin amyloid cardiomyopathy. The Gordian-knot of novel therapeutic regimens.;Cardiology in Review;2021-10-20

5. A low amyloidogenic E61K transthyretin mutation may cause familial amyloid polyneuropathy;Journal of Neurochemistry;2020-09-20