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

Prevalence of alpha1-antitrypsin phenotypes in patients with IgA nephropathy.

Clinical nephrology - 1 Dec 2004

Szönyi L, Dobos M, Vásárhelyi B, Héninger E, Vas T, Nagy J, Kovács T

Abstract excerpt

BACKGROUND: alpha1-antitrypsin (AAT) is the main protease inhibitor in the blood. Several different AAT phenotypes exist. The most common variant is the MM phenotype, which is also associated with normal AAT levels. The less common phenotypes with Z and S variants are associated with low AAT levels. AAT deficiency is a risk factor for pulmonary emphysema, liver impairment and some immune-mediated diseases, some...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to alpha 1-Antitrypsin
Share to alpha 1-Antitrypsin Deficiency

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Glomerulonephritis, IGA

Share to Heterozygote

Share to Kidney Failure, Chronic

Share to Phenotype

Share to Prevalence

Source

Identifiers

PMID: 15630900
DOI: 10.5414/cnp62418

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prevalence of alpha1-antitrypsin phenotypes in patients with IgA nephropathy.PMID 15630900Read ↗

Diagnostic flow chart for targeted detection of alpha1-antitrypsin deficiency.Semantic proximity Read ↗

Distribution of alpha(1)-antitrypsin alleles in patients with bronchiectasis.Semantic proximity Read ↗

α1-Antitrypsin phenotypes and associated serum protein concentrations in a large clinical population.Semantic proximity Read ↗

Association between circulating alpha-1 antitrypsin polymers and lung and liver diseaseSemantic proximity Read ↗

Alpha-1 antitrypsin deficiency hidden in allegedly normal variants.Semantic proximity Read ↗

Genotypes and serum concentrations of human alpha-1-antitrypsin "P" protein variants in a clinical population.Semantic proximity Read ↗

Increased outer arm and core fucose residues on the N-glycans of mutated alpha-1 antitrypsin protein from alpha-1 antitrypsin deficient individuals.Semantic proximity Read ↗

Application of a diagnostic algorithm for the rare deficient variant Mmalton of alpha-1-antitrypsin deficiency: a new approach.Semantic proximity Read ↗

alpha 1-Antitrypsin (AAT) deficiency and ANCA-positive systemic vasculitis: genetic and clinical implications.Semantic proximity Read ↗

A polymorphism of the alpha1-antitrypsin gene represents a risk factor for liver disease.Semantic proximity Read ↗

Three new alpha1-antitrypsin deficiency variants help to define a C-terminal region regulating conformational change and polymerization.Semantic proximity Read ↗

Alpha-1-antitrypsin phenotypes and associated disease patterns in neurological patients.Semantic proximity Read ↗

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