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

Clinical phenotypes and genetic features of hereditary transthyretin amyloidosis patients in China.

Orphanet journal of rare diseases - 2 Sept 2022

He Xinyue, Tian Zhuang, Guan Hongzhi, Zhang Shuyang

Abstract excerpt

BACKGROUND: Hereditary transthyretin amyloidosis (hATTR) is a progressive and fatal disease with heterogenous clinical presentations, limited diagnosis and poor prognosis. This retrospective analysis study aimed to report the genotypes and phenotypes of herediary transthyretin amyloidosis (hATTR) in Chinese through a systematic review of published literature. METHODS: The systematic review included structured...

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 Amyloidosis: Diagnosis, Treatment, Outcomes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Dermatological and Skeletal Disorders

Share to Parathyroid Disorders and Treatments

Share to Phenotype

Share to Prealbumin

Source

Open in PubMed Open full text

Identifiers

PMID: 36056432
DOI: 10.1186/s13023-022-02481-9
PMCID: PMC9438301

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical phenotypes and genetic features of hereditary transthyretin amyloidosis patients in China.PMID 36056432Read ↗

Genetic phenotypes and clinical characteristics description of hereditary transthyretin patients in ChinaSemantic proximity Read ↗

Hereditary transthyretin amyloidosis in mainland China: a unicentric retrospective study.Semantic proximity Read ↗

A Multicenter Study of Hereditary Transthyretin Amyloidosis in ChinaSemantic proximity Read ↗

Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS): 14-year update.Semantic proximity Read ↗

Hereditary transthyretin amyloidosis: a myriad of factors that influence phenotypic variability.Semantic proximity Read ↗

Unique TTR Variants D38A and M13dup Among Korean Patients with Hereditary Transthyretin Amyloidosis: A Retrospective Single-Center Cohort Study.Semantic proximity Read ↗

Hereditary transthyretin cardiac amyloidosis proven by endomyocardial biopsy: a single-centre retrospective study and literature review.Semantic proximity Read ↗

Clinical and genetic profiles of hereditary transthyretin amyloidosis in TaiwanSemantic proximity Read ↗

Genetic and clinical characteristics of hereditary transthyretin amyloidosis in endemic and non-endemic areas: experience from a single-referral center in Japan.Semantic proximity Read ↗

Hereditary transthyretin amyloidosis in multi-ethnic Malaysians.Semantic proximity Read ↗

Hereditary transthyretin amyloidosis overview.Semantic proximity Read ↗

Clinical Practice and Diagnostic Trends in Hereditary Transthyretin Amyloidosis: A 25-Year Observational Study.Semantic proximity Read ↗

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