Evidence map›Paper›PMID 39357506›Full record

ArticleChronic obstructive pulmonary diseases (Miami, Fla.)2024

Alpha-1 Antitrypsin Deficiency in a Young Never Smoker With Novel Pi*Null Homozygous Mutation: a Case Report.

Igor Z Barjaktarevic, Andrew W Hong, Alyssa Hoover, Stanley Nelson, Said Isse, Semi Yoon, Mark Brantley

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Chronic obstructive pulmonary diseases (Miami, Fla.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Igor Z BarjaktarevicDivision of Pulmonary and Critical Care Medicine, University of California, Los Angeles, California, United States.
Andrew W HongDepartment of Medicine, University of California, Los Angeles, California, United States.
Alyssa HooverHuman Genetics, University of California, Los Angeles, California, United States.
Stanley NelsonHuman Genetics, University of California, Los Angeles, California, United States.
Said IsseCleveland Clinic Abu Dhabi, Abu Dhabi,United Arab Emirates.
Semi YoonDivision of Pulmonary and Critical Care Medicine, University of California, Los Angeles, California, United States.
Mark BrantleyDivision of Pulmonary and Critical Care Medicine, University of Florida, Gainesville, Florida, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alpha-1 antitrypsin (AAT) deficiency is an autosomal codominant disorder caused by

Indexed as

alpha-1 antitrypsin deficiencymutationPi*NullSERPINA1

Identifiers

PMID39357506
PMCPMC11703020

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.