Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

When to suspect transthyretin amyloidosis in cases of isolated vitreous opacities?

Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis - 1 Dec 2020

Poignet Barthélémy, Cauquil Cécile, Barreau Emmanuel, Bodaghi Bahram, Terrada Céline, Adams David, Francou Bruno, Labetoulle Marc, Rousseau Antoine

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amyloid Neuropathies, Familial
Share to Eye Diseases
Share to Mutation

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Prealbumin

Share to Tomography, Optical Coherence

Share to Vitreous Body

Source

Identifiers

PMID: 32500742
DOI: 10.1080/13506129.2020.1772744

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

When to suspect transthyretin amyloidosis in cases of isolated vitreous opacities?PMID 32500742Read ↗

Isolated vitreoretinal amyloidosis in the absence of transthyretin mutations.Semantic proximity Read ↗

Vitreous amyloidosis in alanine 71 transthyretin mutation.Semantic proximity Read ↗

Ocular Involvement in Hereditary Amyloidosis.Semantic proximity Read ↗

Vitreal deposits in Val71Ala transthyretin amyloidosis.Semantic proximity Read ↗

Ophthalmological manifestations of hereditary transthyretin amyloidosis.Semantic proximity Read ↗

[Recommendations update for the diagnosis and treatment of transthyretin variant amyloidosis (ATTRv)].Semantic proximity Read ↗

Ophthalmological manifestations in hereditary transthyretin (ATTR V30M) carriers: a review of 513 cases.Semantic proximity Read ↗

Chinese familial transthyretin amyloidosis with vitreous involvement is associated with the transthyretin mutation Gly83Arg: a case report and literature review.Semantic proximity Read ↗

Vitreous Amyloidosis: Ocular, Systemic, and Genetic Insights.Semantic proximity Read ↗

Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis.Semantic proximity Read ↗

Current and Emerging Therapies for Hereditary Transthyretin Amyloidosis: Strides Towards a Brighter FutureSemantic proximity Read ↗

Vitreoretinal Amyloidosis: Clinical Features, OCT/A Insights, Gene Mutations, and Outcomes of Pars Plana Vitrectomy SurgerySemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.