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

[The diagnosis and management of familial amyloid polyneuropathy].

Revue neurologique - 1 Nov 2006

Planté-Bordeneuve V

Abstract excerpt

INTRODUCTION: Familial amyloid polyneuropathy designates a group of dominantly inherited neuropathies, with extracellular deposition of amyloid substance in various tissues. BACKGROUND: The 3 main precursor proteins encountered in these disorders are transthyretin, apolipoprotein A1 or gelsolin. Among them, transthyretin neuropathies are by far the most frequent type with a severe sensori-motor and autonomic...

Read the complete abstract on PubMed

Topics

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

Share to Amyloid
Share to Amyloid Neuropathies, Familial
Share to TTR gene

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

Share to Genotype

Share to Liver Transplantation

Share to Phenotype

Share to Prealbumin

Source

Identifiers

PMID: 17086153
DOI: 10.1016/s0035-3787(06)75130-x

Genes

TTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 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

[The diagnosis and management of familial amyloid polyneuropathy].PMID 17086153Read ↗

[Familial amyloidotic polyneuropathies].Semantic proximity Read ↗

Transthyretin familial amyloid polyneuropathy.Semantic proximity Read ↗

Transthyretin familial amyloid polyneuropathy: an update.Semantic proximity Read ↗

[Transthyretin-related hereditary amyloidosis].Semantic proximity Read ↗

Single-centre experience on transthyretin familial amyloid polyneuropathy: case series and literature review.Semantic proximity Read ↗

Hereditary transthyretin amyloidosis: a comprehensive review with a focus on peripheral neuropathySemantic proximity Read ↗

Recommendations for presymptomatic genetic testing and management of individuals at risk for hereditary transthyretin amyloidosisSemantic proximity Read ↗

[Amyloid polyneuropathies--biochemical and genetic aspects].Semantic proximity Read ↗

[Hereditary transthyretin amyloidosis].Semantic proximity Read ↗

Updates on hereditary transthyretin amyloidosis polyneuropathy.Semantic proximity Read ↗

Guideline of transthyretin-related hereditary amyloidosis for cliniciansSemantic proximity Read ↗

Transthyretin amyloidosis: an under-recognized neuropathy and cardiomyopathySemantic proximity Read ↗

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