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

Slowly progressive descending facial nerve paralysis indicates hereditary gelsolin amyloidosis.

Lancet (London, England) - 17 Jun 2023

Kiernan Miles Finbar, Gillmore Julian D, Gupta Tarang

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 Gelsolin
Share to Mutation

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 37330746
DOI: 10.1016/S0140-6736(23)01063-2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Slowly progressive descending facial nerve paralysis indicates hereditary gelsolin amyloidosis.PMID 37330746Read ↗

Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy.Semantic proximity Read ↗

Teaching NeuroImages: gelsolin-related amyloidosis: a rare cause of progressive facial diparesis.Semantic proximity Read ↗

Familial amyloidotic polyneuropathy type IV--gelsolin amyloidosis.Semantic proximity Read ↗

Gelsolin amyloidosis as a cause of early aging and progressive bilateral facial paralysis.Semantic proximity Read ↗

The First Korean Family With Hereditary Gelsolin Amyloidosis Caused by p.D214Y Mutation in the GSN Gene.Semantic proximity Read ↗

Familial amyloidosis of the Finnish type: clinical and neurophysiological features of two index cases.Semantic proximity Read ↗

Gelsolin-related familial amyloidosis, Finnish type (FAF), and its variants found worldwide.Semantic proximity Read ↗

Natural course of Finnish gelsolin amyloidosis.Semantic proximity Read ↗

Clinical and Histopathological Features of Gelsolin Amyloidosis Associated with a Novel GSN Variant p.Glu580Lys.Semantic proximity Read ↗

Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II.Semantic proximity Read ↗

Hereditary gelsolin amyloidosis mimicking Sjögren's syndrome.Semantic proximity Read ↗

Inherited amyloid polyneuropathy type IV (gelsolin variant) in a Japanese familySemantic proximity Read ↗

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