Evidence map›Paper›PMID 30294303›Full record

ArticleFrontiers in endocrinology2018

An Association of

Emanuela Savarese, Benedetta Di Felice, Francesco Miconi, Gabriele Cabiati, Federica Celi, Francesco Crescenzi, Nicola Principi, Susanna Esposito

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

Article in Frontiers in endocrinology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.1field-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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

8 authors at 3 institutions in 1 country.

Emanuela SavaresePediatric Section, Università degli Studi di Perugia, Perugia, Italy.
Benedetta Di FelicePediatric Section, Università degli Studi di Perugia, Perugia, Italy.
Francesco MiconiPediatric Section, Università degli Studi di Perugia, Perugia, Italy.
Gabriele CabiatiPaediatric Clinic, Azienda Ospedaliera di Terni, Terni, Italy.
Federica CeliPaediatric Clinic, Azienda Ospedaliera di Terni, Terni, Italy.
Francesco CrescenziPaediatric Clinic, Azienda Ospedaliera di Terni, Terni, Italy.
Nicola PrincipiUniversità degli Studi di Milano, Milan, Italy.
Susanna EspositoDepartment of Surgical and Biomedical Sciences, Paediatric Clinic, Università degli Studi di Perugia, Perugia, Italy.
Azienda Ospedaliera San Camillo-Forlanini · ITUniversity of Perugia · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In children with genetic syndromes, short stature is frequently a characteristic feature that, when associated with other specific manifestations, significantly aids in clinical diagnosis. In this report, an atypical case of Noonan syndrome (NS) in a 5.5-year-old child with mesomelic short stature is described. Genetic tests revealed two different mutations in this child. As expected in an NS case, a mutation in

Indexed as

failure to thrivegrowth hormoneNoonan syndromeshort statureSHOX gene

Identifiers

PMID30294303
PMCPMC6158368
OpenAlexW2891071632

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.