Evidence map›Paper›PMID 36320799›Full record

ArticleCureus2022

Heterozygous Mutation of Sodium Voltage-Gated Channel Alpha Subunit 2 and Pumilio Homolog 1 Genes in a Pediatric Patient: A Case Report.

Fawzia Al-Sharif, Feryal O Attiah, Nada A AlKhateeb, Hussein O Taher, Mohammed F Alamer, Raneem Y Gazzaz, Muayad O Ba Sahel, Rena M Alsharif

Abstract readCase Reports
In one paragraph

Article in Cureus, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Fawzia Al-SharifPediatrics, Saudi German Hospital Jeddah, Jeddah, SAU.
Feryal O AttiahMedicine, King Abdulaziz University Hospital, Jeddah, SAU.
Nada A AlKhateebMedicine, King Abdulaziz University Hospital, Jeddah, SAU.
Hussein O TaherMedicine, Batterjee Medical College, Jeddah, SAU.
Mohammed F AlamerMedicine, Batterjee Medical College, Jeddah, SAU.
Raneem Y GazzazMedicine, Batterjee Medical College, Jeddah, SAU.
Muayad O Ba SahelMedicine, Batterjee Medical College, Jeddah, SAU.
Rena M AlsharifMedicine, College of Medicine, Umm Al-Qura University, Mecca, SAU.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epilepsy is a neurological condition brought on by recurrent and spontaneous seizures in patients with hypersynchronous neuronal ensemble activity. These spontaneous seizures appear to be brought on by increased neuronal excitability and synaptic synchronization. The development of neuronal hyperexcitability and acquiring epilepsy is still poorly understood. Cell differentiation and development might be related to the pumilio RNA-binding family member 1 (Pumilio 1 (

Indexed as

epilepsypum1rna-binding proteinscn2seizures

Identifiers

PMID36320799
PMCPMC9603888

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.