Evidence map›Paper›PMID 29439187›Full record

ArticleHaematologica2018

Lethal neonatal bone marrow failure syndrome with multiple congenital abnormalities, including limb defects, due to a constitutional deletion of 3'

Lars T van der Veken, Merel C Maiburg, Floris Groenendaal, Mariëlle E van Gijn, Andries C Bloem, Claudia Erpelinck, Stefan Gröschel, Mathijs A Sanders, Ruud Delwel, Marc B Bierings and 1 more

Abstract readCase Reports
In one paragraph

Article in Haematologica, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Perinatal-lethal nonimmune fetal hydrops attributed toCold Spring Harbor molecular case studies · 2023
    Article
  9. Article
  10. Review
  11. Review
  12. 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

11 authors.

Lars T van der VekenDepartment of Genetics, University Medical Center Utrecht, Wilhelmina Children's Hospital, Utrecht University, Rotterdam, the Netherlands.
Merel C MaiburgDepartment of Genetics, University Medical Center Utrecht, Wilhelmina Children's Hospital, Utrecht University, Rotterdam, the Netherlands.
Floris GroenendaalDepartment of Neonatology, University Medical Center Utrecht, Wilhelmina Children's Hospital, Utrecht University, Rotterdam, the Netherlands.
Mariëlle E van GijnDepartment of Genetics, University Medical Center Utrecht, Wilhelmina Children's Hospital, Utrecht University, Rotterdam, the Netherlands.
Andries C BloemDepartment of Immunology, University Medical Center Utrecht, Wilhelmina Children's Hospital, Utrecht University, Rotterdam, the Netherlands.
Claudia ErpelinckDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Stefan GröschelDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Mathijs A SandersDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Ruud DelwelDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Marc B BieringsDepartment of Pediatric Hematology and stem cell transplantation, University Medical Center Utrecht, Wilhelmina Children's Hospital, Utrecht University, the Netherlands.
Arjan BuijsDepartment of Genetics, University Medical Center Utrecht, Wilhelmina Children's Hospital, Utrecht University, Rotterdam, the Netherlands a.buijs@umcutrecht.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Abnormalities, MultipleAmino Acid SequenceAnemia, AplasticBone Marrow DiseasesBone Marrow Failure DisordersHemoglobinuria, ParoxysmalHumansInfant, NewbornMagnetic Resonance ImagingMaleMDS1 and EVI1 Complex Locus ProteinSequence DeletionTomography, X-Ray ComputedMDS1 and EVI1 Complex Locus ProteinMECOM protein, human

Identifiers

PMID29439187
PMCPMC5865425

What OpenQuestion holds

Textmetadata
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.