Evidence map›Paper›PMID 32076552›Full record

ArticleRespirology case reports2020

Clinical manifestations in patients with PI*MM

Marina Aiello, Alberto Fantin, Chiara Longo, Ilaria Ferrarotti, Giuseppina Bertorelli, Alfredo Chetta

Open access · goldAbstract readCase Reports
In one paragraph

Article in Respirology case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 45% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Variants ofTherapeutic advances in chronic disease · 2021
    Review
  9. Clinical manifestations in patients with PI*MMRespirology case reports · 2020
    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

6 authors at 2 institutions in 1 country.

Marina AielloDepartment of Medicine and Surgery, Respiratory Disease and Lung Function Unit University of Parma Italy.ORCID https://orcid.org/0000-0003-0636-5345
Alberto FantinDepartment of Medicine and Surgery, Respiratory Disease and Lung Function Unit University of Parma Italy.ORCID https://orcid.org/0000-0002-5707-775X
Chiara LongoDepartment of Medicine and Surgery, Respiratory Disease and Lung Function Unit University of Parma Italy.
Ilaria FerrarottiCenter for the Diagnosis of Inherited Alpha1-antitrypsin Deficiency, Department of Internal Medicine and Therapeutics, Pneumology Unit University of Pavia Italy.
Giuseppina BertorelliDepartment of Medicine and Surgery, Respiratory Disease and Lung Function Unit University of Parma Italy.
Alfredo ChettaDepartment of Medicine and Surgery, Respiratory Disease and Lung Function Unit University of Parma Italy.
University of Parma · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the genetic variants associated with alpha-1 antitrypsin deficiency (AATD) in 117 patients admitted to our outpatient clinic and characterized by a serum concentration of AAT lower than 113 mg/dL. We focused on the M-like heterozygous variant of the

Indexed as

Alpha‐1 antitrypsin deficiencygenotypelung and liver function

Identifiers

PMID32076552
PMCPMC7029433
OpenAlexW3008119728

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.