Evidence map›Paper›PMID 28914431›Full record

ArticleJournal of community genetics2017

A rare disorder or not? How a child with jaundice changed a nationwide regimen in the Netherlands.

E A L van den Heuvel, A Baauw, S J Mensink-Dillingh, M Bartels

Abstract read
In one paragraph

Article in Journal of community genetics, 2017. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Article
  4. Genomics for all in the 21st century?Journal of community genetics · 2017
    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

4 authors.

E A L van den HeuvelDepartment of Pediatrics, Gelderse Vallei Hospital, Ede, the Netherlands. E.A.L.vandenHeuvel@umcutrecht.nl.ORCID http://orcid.org/0000-0003-0056-5485
A BaauwDepartment of Pediatrics, Rijnstate Hospital, Arnhem, the Netherlands.
S J Mensink-DillinghDepartment of Pediatrics, Gelderse Vallei Hospital, Ede, the Netherlands.
M BartelsDepartment of Pediatric Hematology and Stem Cell Transplantation, University Medical Center Utrecht, Lundlaan 6, 3508, AB, Utrecht, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to global migration, there is an increased frequency of diseases, which used to be rare in Western countries. Here, we describe a striking case in order to create awareness for diseases that are known for decades but sometimes "forgotten" in Western countries, including glucose-6-phosphate dehydrogenase deficiency. We will discuss how everyday practice can lead to serious medical problems and present general recommendations to support.

Identifiers

PMID28914431
PMCPMC5614890

What OpenQuestion holds

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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.