Evidence map›Paper›PMID 32779500›Full record

ReviewThe Journal of international medical research2020

A patient with glycogen storage disease type 0 and a novel sequence variant in

Janez Jan Arko, Marusa Debeljak, Mojca Zerjav Tansek, Tadej Battelino, Urh Groselj

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

Review in The Journal of international medical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. NovelMolecular genetics and metabolism reports · 2021
    Article
  5. Article
  6. Review
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 2 institutions in 1 country.

Janez Jan ArkoThe Division of Internal Medicine, UMC Ljubljana, Ljubljana, Slovenia.ORCID https://orcid.org/0000-0001-9341-5122
Marusa DebeljakClinical Institute for Special Laboratory Diagnostics, University Children's Hospital, UMC Ljubljana, Ljubljana, Slovenia.
Mojca Zerjav TansekFaculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Tadej BattelinoFaculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Urh GroseljFaculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.ORCID https://orcid.org/0000-0002-5246-9869
University of Ljubljana · SILjubljana University Medical Centre · SI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glycogen storage disease type 0 (GSD0) is an autosomal recessive disorder caused by a sequence variant in the

Indexed as

Glycogen Storage DiseaseHyperglycemiaHypoglycemiaFemaleGlycogen SynthaseHumansInfantPhenotypeGlycogen Synthasegene sequence variantGlycogen storage disease type 0GSDGYS2hepatic glycogen synthasehyperketotic hypoglycemia

Identifiers

PMID32779500
PMCPMC7425267
OpenAlexW3048915713

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.