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

Familial meningocerebrovascular amyloidosis, Hungarian type, with mutant transthyretin (TTR Asp18Gly)

1 Dec 1996

Abstract excerpt

Amyloid deposits in leptomeningeal vessels, subarachnoid, subpial, and subependymal cerebrospinal regions, spinal ganglia, peripheral nerves, and some internal organs (predominantly heart and kidney) characterize a dominantly inherited disease in a Hungarian family. We found four definitely and three probably affected members in this family of 56 persons in four generations. Clinical features in all definitely...

Read the complete abstract on PubMed

Topics

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

Share to Amyloidosis: Diagnosis, Treatment, Outcomes
Share to Dermatological and Skeletal Disorders
Share to Peptidase Inhibition and Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 8960746
DOI: 10.1212/wnl.47.6.1562

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial meningocerebrovascular amyloidosis, Hungarian type, with mutant transthyretin (TTR Asp18Gly)PMID 8960746Read ↗

Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD 18G)Semantic proximity Read ↗

Central Nervous System Manifestations Associated with Hereditary Transthyretin Amyloidosis: a Narrative Review.Semantic proximity Read ↗

Transthyretin amyloidosis: a new mutation associated with dementia.Semantic proximity Read ↗

Current Review of Leptomeningeal Amyloidosis Associated With Transthyretin Mutations.Semantic proximity Read ↗

Oculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patient.Semantic proximity Read ↗

TTR associated leptomeningeal amyloidosis in a Sri Lankan patient.Semantic proximity Read ↗

Neuropathology of central nervous system involvement in TTR amyloidosis.Semantic proximity Read ↗

Transthyretin amyloidosis and superficial siderosis of the CNS.Semantic proximity Read ↗

An autopsy case of leptomeningeal amyloidosis associated with transthyretin Gly47Arg mutation.Semantic proximity Read ↗

Unifying features of systemic and cerebral amyloidosis.Semantic proximity Read ↗

Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis.Semantic proximity Read ↗

Neuroradiologic and clinicopathologic features of oculoleptomeningeal type amyloidosis.Semantic proximity Read ↗

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