Evidence map›Paper›PMID 32256629›Full record

ArticleIranian journal of child neurology2020

Non-progressive Nonimmune Hydrops Fetalis Caused by a Novel Mutation in

Asieh Mosallanejad, Mohammadreza Alaei, Saeed Reza Ghaffari, Maryam Rafati, Hedyeh Saneifard

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

Article in Iranian journal of child neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. MPS VII - Extending the classical phenotype.Molecular genetics and metabolism reports · 2022
    Article
  2. Epidemiology of Mucopolysaccharidoses Update.Diagnostics (Basel, Switzerland) · 2021
    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 3 institutions in 1 country.

Asieh MosallanejadDepartment of Pediatric Endocrinology and Metabolic diseases, Mofid children hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mohammadreza AlaeiDepartment of Pediatric Endocrinology and Metabolic diseases, Mofid children hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Saeed Reza GhaffariReproductive Biotechnology Research Center, Avicenna Research Institute, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Maryam RafatiReproductive Biotechnology Research Center, Avicenna Research Institute, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Hedyeh SaneifardDepartment of Pediatric Endocrinology and Metabolic diseases, Mofid children hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Shahid Beheshti University of Medical Sciences · IRAcademic Center for Education, Culture and Research · IRBiotechnology Research Center · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

GUSB GeneHydrops FetalisMucopolysaccharidosisSly Syndrome

Identifiers

PMID32256629
PMCPMC7085123
OpenAlexW3010929383

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.