Evidence map›Paper›PMID 36447760›Full record

ArticleACG case reports journal2022

An Unexpected Anemia Hiding a Rare Syndrome With Overlapping Phenotypes.

Arianna Dal Buono, Laura Poliani, Alessandro Repici, Cesare Hassan, Paolo Bianchi

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

Article in ACG case reports journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 49% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

5 authors at 3 institutions in 1 country.

Arianna Dal BuonoGastroenterology and Digestive Endoscopy Unit, Department of Gastroenterology, Humanitas Research Hospital, Rozzano (Milan), Italy.ORCID https://orcid.org/0000-0002-8543-4355
Laura PolianiGastroenterology and Digestive Endoscopy Unit, Department of Gastroenterology, Humanitas Research Hospital, Rozzano (Milan), Italy.
Alessandro RepiciGastroenterology and Digestive Endoscopy Unit, Department of Gastroenterology, Humanitas Research Hospital, Rozzano (Milan), Italy.
Cesare HassanGastroenterology and Digestive Endoscopy Unit, Department of Gastroenterology, Humanitas Research Hospital, Rozzano (Milan), Italy.
Paolo BianchiClinical Analysis Laboratory, Oncological Molecular Genetics Section, Humanitas Research Hospital-IRCCS, Rozzano (Milan), Italy.ORCID https://orcid.org/0000-0001-5786-5644
Humanitas University · ITIRCCS Humanitas Research Hospital · ITIRCCS Ospedale San Raffaele · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric polyposis is a rare endoscopic finding that can imply genetic syndromes predisposing to cancer development. Among the possible conditions associated with gastric polyposis and early onset gastric cancer (younger than 45 years) is juvenile polyposis syndrome. We present a clinical case of early onset gastric cancer associated with a frameshift mutation in the gene

Identifiers

PMID36447760
PMCPMC9699651
OpenAlexW4310597517

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.