Evidence map›Paper›PMID 35433011›Full record

ArticleRespirology case reports2022

Clinical manifestations of a new alpha-1 antitrypsin genetic variant:

Marina Aiello, Annalisa Frizzelli, Laura Marchi, Ilaria Ferrarotti, Davide Piloni, Giovanna Pelà, Alessandro De Simoni, Lorenzo D'Aloisio, Luigino Calzetta, Alfredo Chetta

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Respirology case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 52% of its field
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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Characterization of three newRespiratory medicine case reports · 2023
    Article
  2. 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

10 authors at 3 institutions in 2 countries.

Marina AielloDepartment of Medicine and Surgery, Respiratory Disease and Lung Function Unit University of Parma Parma Italy.
Annalisa FrizzelliDepartment of Medicine and Surgery, Respiratory Disease and Lung Function Unit University of Parma Parma Italy.
Laura MarchiDepartment of Food and Drug University of Parma Parma Italy.ORCID https://orcid.org/0000-0002-5973-4901
Ilaria FerrarottiCenter for the Diagnosis of Inherited Alpha1-Antitrypsin Deficiency, Department of Internal Medicine and Therapeutics, Pneumology Unit University of Pavia Pavia Italy.
Davide PiloniUnit of Respiratory Diseases, Department of Medical Sciences and Infective Diseases IRCCS Policlinico San Matteo Foundation Pavia Italy.
Giovanna PelàDepartment of Medicine and Surgery University of Parma Parma Italy.
Alessandro De SimoniDepartment of Medicine and Surgery, Respiratory Disease and Lung Function Unit University of Parma Parma Italy.
Lorenzo D'AloisioDepartment of Medicine and Surgery, Respiratory Disease and Lung Function Unit University of Parma Parma Italy.
Luigino CalzettaDepartment of Medicine and Surgery, Respiratory Disease and Lung Function Unit University of Parma Parma Italy.
Alfredo ChettaDepartment of Medicine and Surgery, Respiratory Disease and Lung Function Unit University of Parma Parma Italy.
University of Parma · ITIntensive Care Foundation · AUUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alpha-1 antitrypsin deficiency is an autosomal, codominant disorder caused by mutations of the

Indexed as

alpha‐1 antitrypsin deficiencyclinical manifestationsgenotypevariant

Identifiers

PMID35433011
PMCPMC9008433
OpenAlexW4223966292

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.