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 features of individuals with PI*SZ phenotype of alpha 1-antitrypsin deficiency. alpha 1-Antitrypsin Deficiency Registry Study Group.

American journal of respiratory and critical care medicine - 1 Dec 1996

Turino G M, Barker A F, Brantly M L, Cohen A B, Connelly R P, Crystal R G, Eden E, Schluchter M D, Stoller J K

Abstract excerpt

This report describes the clinical characteristics of a group of 59 individuals with the PI*SZ phenotype and alpha 1-antitrypsin (alpha 1-AT) deficiency, identified during recruitment of a registry for subjects with severe alpha 1-antitrypsin deficiency. Currently, 1,129 individuals with levels of alpha 1-AT of 11 microM or below have been enrolled in this registry. Individuals with the SZ phenotype whose alpha...

Read the complete abstract on PubMed

Topics

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

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 Forced Expiratory Volume

Share to Lung Diseases, Obstructive

Share to Phenotype

Share to Risk Factors

Share to Smoking

Source

Identifiers

PMID: 8970361
DOI: 10.1164/ajrccm.154.6.8970361

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

Clinical features of individuals with PI*SZ phenotype of alpha 1-antitrypsin deficiency. alpha 1-Antitrypsin Deficiency Registry Study Group.PMID 8970361Read ↗

Clinical considerations in individuals with α1-antitrypsin PI*SZ genotype.Semantic proximity Read ↗

Alpha-1 antitrypsin Pi*SZ genotype: estimated prevalence and number of SZ subjects worldwide.Semantic proximity Read ↗

Risk of lung disease in the PI*SS genotype of alpha-1 antitrypsin: an EARCO research project.Semantic proximity Read ↗

Prevalence of α1-antitrypsin PiZZ genotypes in patients with COPD in Europe: a systematic review.Semantic proximity Read ↗

Estimated Worldwide Prevalence of the PI*ZZ Alpha-1 Antitrypsin Genotype in Subjects With Chronic Obstructive Pulmonary Disease.Semantic proximity Read ↗

Spanish Registry of Patients With Alpha-1 Antitrypsin Deficiency; Comparison of the Characteristics of PISZ and PIZZ Individuals.Semantic proximity Read ↗

PiSZ alpha-1 antitrypsin deficiency (AATD): pulmonary phenotype and prognosis relative to PiZZ AATD and PiMM COPD.Semantic proximity Read ↗

Clinical phenotypes of Italian and Spanish patients with α1-antitrypsin deficiency.Semantic proximity Read ↗

SZ alpha-1 antitrypsin deficiency and pulmonary disease: more like MZ, not like ZZ.Semantic proximity Read ↗

PI SZ phenotype in chronic obstructive pulmonary disease.Semantic proximity Read ↗

Comparison among populations with severe and intermediate alpha1-antitrypsin deficiency and chronic obstructive pulmonary disease.Semantic proximity Read ↗

Molecular diagnosis of intermediate and severe alpha(1)-antitrypsin deficiency: MZ individuals with chronic obstructive pulmonary disease may have lower lung function than MM individuals.Semantic proximity Read ↗

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