Evidence map›Paper›PMID 33777149›Full record

ArticleInternational journal of pediatrics2021

Case Report of RANBP2 Mutation and Familial Acute Necrotizing Encephalopathy.

Mohamad Paktinat, Kamran Hessami, Soroor Inaloo, Hamid Nemati, Pegah Katibeh, Marzieh Nejabat, Mohammad Hassan Darabi, Ali Hosseini Bereshneh

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

Article in International journal of pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 40% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. 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

8 authors at 1 institution in 1 country.

Mohamad PaktinatNeonatology Research Center, Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Kamran HessamiStudent Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID https://orcid.org/0000-0003-1722-3553
Soroor InalooNeonatology Research Center, Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Hamid NematiNeonatology Research Center, Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Pegah KatibehNeonatology Research Center, Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Marzieh NejabatNeonatology Research Center, Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Mohammad Hassan DarabiStudent Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
Ali Hosseini BereshnehPrenatal Diagnosis and Genetic Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Shiraz University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAcute necrotizing encephalopathy (ANE), a rare entity with unique clinical presentation, can be associated significant morbidity and mortality. The majority of ANE reported cases are sporadic. However, reports of extremely rare familial cases are scarce.

conclusionThe presented cases are the first reports of familial ANE in Iran. Attempt was made to raise awareness on this disease, because high clinical suspicion plays an important role in the early diagnosis and proper management of these patients.

Identifiers

PMID33777149
PMCPMC7981175
OpenAlexW3136313641

What OpenQuestion holds

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LicenceCC BY
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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.