OCULAR MANIFESTATIONS OF ASP38ALA AND THR59LYS FAMILIAL TRANSTHYRETIN AMYLOIDOSIS-Reference-Cited by-同舟云学术

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OCULAR MANIFESTATIONS OF ASP38ALA AND THR59LYS FAMILIAL TRANSTHYRETIN AMYLOIDOSIS

Published:2022-02 Issue:2 Volume:42 Page:396-403
ISSN:0275-004X
Container-title:Retina
language:en
Short-container-title:

Author:

Choi Kyung Jun,Son Ki Young,Kang Se Woong,Kim Darae,Choi Jin Oh,Kim Hee Jin,Kim Jung Sun,Jeon Eun Seok,Kim A Young,Kang Min Chae,Kim Sang Jin

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology,General Medicine

Reference29 articles.

1. Nomenclature 2014: amyloid fibril proteins and clinical classification of the amyloidosis;Sipe;Amyloid,2014

2. Systemic amyloidosis;Wechalekar;Lancet,2016

3. The molecular biology and clinical features of amyloid neuropathy;Benson;Muscle Nerve,2007

4. Guideline of transthyretin-related hereditary amyloidosis for clinicians;Ando;Orphanet J Rare Dis,2013

5. Synthesis and secretion of retinol-binding protein and transthyretin by cultured retinal pigment epithelium;Ong;Biochemistry,1994

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1. Cornea and Sclera;Ocular Pathology;2025

2. Rare manifestation of familial vitreous amyloidosis caused by Gly103Arg transthyretin;International Journal of Ophthalmology;2023-07-18

3. Genetic Aspects of Glaucoma: An Updated Review;Current Molecular Medicine;2023-06-02

4. Application of optical coherence tomography angiography to assess systemic severity in patients with hereditary transthyretin amyloidosis;PLOS ONE;2022-09-26

5. Case Report: Hereditary transthyretin (ATTRv) amyloidosis: The p.G103R mutation of the transthyretin gene in a Han Chinese family is associated with vitreous hemorrhage;Frontiers in Genetics;2022-09-15

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