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

Valve-sparing Aortic Root Replacement for a Patient With Filamin A Mutation.

The Annals of thoracic surgery - 1 May 2022

Yamazaki Kazuhiro, Minatoya Kenji, Kumagai Motoyuki, Handa Tomohiro, Ohsumi Akihiro, Torishima Masako, Kawasaki Hidenori

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 Aorta
Share to Aortic Valve
Share to Filamins
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Treatment Outcome

Source

Identifiers

PMID: 35032450
DOI: 10.1016/j.athoracsur.2021.12.037

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

Valve-sparing Aortic Root Replacement for a Patient With Filamin A Mutation.PMID 35032450Read ↗

Filamin A mitral valve disease: prolapse, dystrophy, or dysplasia?Semantic proximity Read ↗

Asymmetrical aortic root aneurism in patient with Filamin A mutation.Semantic proximity Read ↗

Familial cardiac valvulopathy due to filamin A mutation.Semantic proximity Read ↗

Filamin A heart valve disease as a genetic cause of inherited bicuspid and tricuspid aortic valve diseaseSemantic proximity Read ↗

Dilated Cardiomyopathy: New Variant in the Filamin-C Gene.Semantic proximity Read ↗

Filamin-a-related myxomatous mitral valve dystrophy: genetic, echocardiographic and functional aspects.Semantic proximity Read ↗

A review of filamin A mutations and associated interstitial lung diseaseSemantic proximity Read ↗

Mutations in the gene encoding filamin A as a cause for familial cardiac valvular dystrophy.Semantic proximity Read ↗

New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome study.Semantic proximity Read ↗

Combined cardiological and neurological abnormalities due to filamin A gene mutation.Semantic proximity Read ↗

Expression of the familial cardiac valvular dystrophy gene, filamin‐A, during heart morphogenesisSemantic proximity Read ↗

Filamin A: phenotypic diversity.Semantic proximity Read ↗

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