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

Inherited amyloid polyneuropathy type IV (gelsolin variant) in a Japanese family

1 Jan 1993

Abstract excerpt

We describe a Japanese family with familial amyloid polyneuropathy type IV. The family originates from central Japan, Nagano prefecture, and is unrelated to Finnish or other Caucasian populations. Of 42 members in three generations, 14 individuals (5 men, 9 women) are affected by corneal lattice dystrophy, cranial neuropathy, mild peripheral neuropathy, and skin changes. Polarizing microscopy and...

Read the complete abstract on PubMed

Topics

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

Share to Alzheimer's disease research and treatments
Share to Amyloidosis: Diagnosis, Treatment, Outcomes
Share to Dermatological and Skeletal Disorders

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

Source

Identifiers

PMID: 8388189
DOI: 10.1002/ana.410330110

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

Inherited amyloid polyneuropathy type IV (gelsolin variant) in a Japanese familyPMID 8388189Read ↗

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

[Gene analysis of Japanese patients with familial amyloidotic polyneuropathy type IV].Semantic proximity Read ↗

Familial amyloid polyneuropathy (Finnish type) in a Japanese family: Clinical features and immunocytochemical studies.Semantic proximity Read ↗

Finnish type of familial amyloidosis: cosegregation of Asp187----Asn mutation of gelsolin with the disease in three large families.Semantic proximity Read ↗

Isolation and characterization of cardiac amyloid in familial amyloid polyneuropathy type IV (Finnish): relation of the amyloid protein to variant gelsolin.Semantic proximity Read ↗

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

Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type)Semantic proximity Read ↗

[Familial amyloidosis, Finnish type with marked anhidrosis].Semantic proximity Read ↗

Hereditary amyloidosis of the Finnish type in a German family: clinical and electrophysiological presentation.Semantic proximity Read ↗

Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type.Semantic proximity Read ↗

Gelsolin-related amyloidosis. Identification of the amyloid protein in Finnish hereditary amyloidosis as a fragment of variant gelsolin.Semantic proximity Read ↗

[Clinical pathology and molecular genetics on familial amyloidotic polyneuropathy].Semantic proximity Read ↗

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