ATTRv amyloidosis Italian Registry: clinical and epidemiological data.

doi:10.1080/13506129.2020.1794807

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

Community

Back to search

Article

ATTRv amyloidosis Italian Registry: clinical and epidemiological data.

Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis - 1 Dec 2020

Russo Massimo, Obici Laura, Bartolomei Ilaria, Cappelli Francesco, Luigetti Marco, Fenu Silvia, Cavallaro Tiziana, Chiappini Maria Grazia, Gemelli Chiara, Pradotto Luca Guglielmo, Manganelli Fiore, Leonardi Luca, My Filomena, Sampaolo Simone, Briani Chiara, Gentile Luca, Stancanelli Claudia, Di Buduo Eleonora, Pacciolla Paolo, Salvi Fabrizio, Casagrande Silvia, Bisogni Giulia, Calabrese Daniela, Vanoli Fiammetta, Di Iorio Giuseppe, Antonini Giovanni, Santoro Lucio, Mauro Alessandro, Grandis Marina, Di Girolamo Marco, Fabrizi Gian Maria, Pareyson Davide, Sabatelli Mario, Perfetto Federico, Rapezzi Claudio, Merlini Giampaolo, Mazzeo Anna, Vita Giuseppe

Abstract excerpt

INTRODUCTION: ATTRv amyloidosis is worldwide spread with endemic foci in Portugal and Sweden, Japan, Brazil, Maiorca, and Cyprus. A national Registry was developed to characterise the epidemiology and genotype-phenotype correlation of ATTRv amyloidosis in Italy and to allow a better planning of diagnostic and therapeutic services. METHODS: Fifteen Italian referral centres for amyloidosis spread all over the...

Read the complete abstract on PubMed

Topics

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Aged, 80 and over

Share to Amyloid Neuropathies, Familial

Share to Cardiomyopathies

Share to Italy

Share to Polyneuropathies

Share to Prealbumin

Share to Prevalence

Share to Registries

Source

Open in PubMed

Identifiers

PMID: 32696671
DOI: 10.1080/13506129.2020.1794807

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

ATTRv amyloidosis Italian Registry: clinical and epidemiological data.PMID 32696671Read ↗

A description of variant transthyretin amyloidosis (ATTRv) stage 1 patients and asymptomatic carriers in Spain: the EMPATIa study.Semantic proximity Read ↗

Clinical features of TTR-FAP in PortugalSemantic proximity Read ↗

Clinical and genetic profiles of patients with hereditary and wild-type transthyretin amyloidosis: the Transthyretin Cardiac Amyloidosis Registry in the state of São Paulo, Brazil (REACT-SP)Semantic proximity Read ↗

Online registry for mutations in hereditary amyloidosis including nomenclature recommendations.Semantic proximity Read ↗

Changes in amyloidosis phenotype over 11 years in a cardiac amyloidosis referral centre cohort in France.Semantic proximity Read ↗

Characterization and natural history of different phenotypes in hereditary transthyretin amyloidosis: 40-year experience at a single Italian referral centre.Semantic proximity Read ↗

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

Epidemiology of variant transthyretin amyloidosis at a reference center in Argentina.Semantic proximity Read ↗

Transthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP): A Single-Center Experience in Sicily, an Italian Endemic AreaSemantic proximity Read ↗

Clinical and Phenotypic Characterization of Hereditary Transthyretin Amyloidosis (ATTRv) in Peruvian Population: First Case Series IMPAC-FE StudySemantic proximity Read ↗

Spectrum of hereditary transthyretin amyloidosis due to T60A(p.Thr80Ala) variant in an Irish Amyloidosis Network.Semantic proximity Read ↗

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