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

Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis.

Journal of neurology - 1 Oct 2012

Briani Chiara, Cavallaro Tiziana, Ferrari Sergio, Taioli Federica, Calamelli Sara, Verga Laura, Adami Fausto, Fabrizi Gian Maria

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 Amyloidosis
Share to Biopsy
Share to Cardiomyopathy, Restrictive

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

Share to Coronary Artery Disease

Share to Diagnostic Errors

Share to Magnetic Resonance Imaging

Share to Prealbumin

Source

Identifiers

PMID: 22580845
DOI: 10.1007/s00415-012-6529-z

Genes

TTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 18 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

Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis.PMID 22580845Read ↗

A late-onset case of hereditary transthyretin amyloidosis with a novel compound heterozygous mutation.Semantic proximity Read ↗

Not So Rare After All: Rethinking Hereditary Transthyretin AmyloidosisSemantic proximity Read ↗

Hereditary transthyretin amyloidosis overview.Semantic proximity Read ↗

Hereditary transthyretin amyloidosis associated with a transthyretin variant Thr59Arg.Semantic proximity Read ↗

A novel TTR mutation (p.Ala65Val) underlying late-onset hereditary transthyretin (ATTRv) amyloidosis with mixed cardiac and neuropathic phenotype: a case report.Semantic proximity Read ↗

Hereditary transthyretin amyloidosisSemantic 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 ↗

An aggressive form of transthyretin amyloidosis.Semantic proximity Read ↗

Frequencies and geographic distributions of genetic mutations in transthyretin- and non-transthyretin-related familial amyloidosis.Semantic proximity Read ↗

A new transthyretin mutation associated with leptomeningeal amyloidosis.Semantic proximity Read ↗

Transthyretin mutagenesis: impact on amyloidogenesis and disease.Semantic proximity Read ↗

Transthyretin mutations in hyperthyroxinemia and amyloid diseases.Semantic proximity Read ↗

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