Evidence map›Paper›PMID 38304750›Full record

ArticleFrontiers in pediatrics2024

Mild phenotype of

Aysylu Murtazina, Artem Borovikov, Andrey Marakhonov, Artem Sharkov, Inna Sharkova, Alena Mirzoyan, Sviatlana Kulikova, Ralina Ganieva, Viktoriia Zabnenkova, Oksana Ryzhkova and 3 more

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

Article in Frontiers in pediatrics, 2024. 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
1.5field-weighted citation impact, top 19% 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, 4 citations in OpenAlex.

  1. Article
  2. 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

13 authors at 3 institutions in 2 countries.

Aysylu MurtazinaResearch Centre for Medical Genetics, Moscow, Russia.
Artem BorovikovResearch Centre for Medical Genetics, Moscow, Russia.
Andrey MarakhonovResearch Centre for Medical Genetics, Moscow, Russia.
Artem SharkovVeltischev Research and Clinical Institute for Pediatrics of the Pirogov Russian National Research Medical University, Moscow, Russia.
Inna SharkovaResearch Centre for Medical Genetics, Moscow, Russia.
Alena MirzoyanRepublican Research and Clinical Center of Neurology and Neurosurgery, Minsk, Belarus.
Sviatlana KulikovaRepublican Research and Clinical Center of Neurology and Neurosurgery, Minsk, Belarus.
Ralina GanievaResearch Centre for Medical Genetics, Moscow, Russia.
Viktoriia ZabnenkovaResearch Centre for Medical Genetics, Moscow, Russia.
Oksana RyzhkovaResearch Centre for Medical Genetics, Moscow, Russia.
Sergey NikitinResearch Centre for Medical Genetics, Moscow, Russia.
Elena DadaliResearch Centre for Medical Genetics, Moscow, Russia.
Sergey KutsevResearch Centre for Medical Genetics, Moscow, Russia.
Research Centre for Medical Genetics · RURepublican Scientific and Practical Center of Neurology and Neurosurgery · BYPirogov Russian National Research Medical University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital myasthenic syndrome with episodic apnea is associated with pathogenic variants in the

Indexed as

case reportCHATCMScongenital myasthenic syndromemild phenotype

Identifiers

PMID38304750
PMCPMC10830679
OpenAlexW4390980165

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.