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

Cirrhosis and Portal Hypertension in Compound Heterozygous People With Cystic Fibrosis Harboring One F508del CFTR Gene Mutation.

Gastroenterology - 1 Oct 2022

Duursma Sanne S, Verkade Henkjan J, Bodewes Frank A J A

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 Benzodioxoles
Share to Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator
Share to Hypertension, Portal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Liver Cirrhosis

Share to Mutation

Source

Identifiers

PMID: 35697137
DOI: 10.1053/j.gastro.2022.06.019

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cirrhosis and Portal Hypertension in Compound Heterozygous People With Cystic Fibrosis Harboring One F508del CFTR Gene Mutation.PMID 35697137Read ↗

Liver cirrhosis and portal hypertension in cystic fibrosis.Semantic proximity Read ↗

Liver cirrhosis and portal hypertension in cystic fibrosis.Semantic proximity Read ↗

Cirrhotic Cardiomyopathy: A New Clinical Phenotype.Semantic proximity Read ↗

Characterization of CFTR mutations in people with cystic fibrosis and severe liver disease who are not eligible for CFTR modulators.Semantic proximity Read ↗

An autosomal dominant form of non-cirrhotic portal hypertension.Semantic proximity Read ↗

Screening for liver disease in cystic fibrosis: analysis of clinical and genetic risk factors for its development.Semantic proximity Read ↗

Cystic fibrosis transmembrane conductance regulator (CFTR) gene defects in patients with primary sclerosing cholangitis.Semantic proximity Read ↗

Causes of liver disease in an adult population with heterozygous and homozygous alpha 1-antitrypsin deficiency.Semantic proximity Read ↗

Isolated liver disease in a patient with a CFTR genotype F508del/12TG-5T and 470MV: A new face of an old disease.Semantic proximity Read ↗

[Heterozygous alpha-1-antitrypsin deficiency (PiMZ): risk factor in the development of primary liver carcinoma in non-cirrhotic liver?].Semantic proximity Read ↗

Novel missense mutation (G314R) in a cystic fibrosis patient with hepatic failure.Semantic proximity Read ↗

Primary sclerosing cholangitis is associated with abnormalities in CFTR.Semantic proximity Read ↗

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