Evidence map›Paper›PMID 37374260›Full record

ArticleMedicina (Kaunas, Lithuania)2023

A Rare Co-Occurrence of Maffucci Syndrome and Astrocytoma with IDH1 R132H Mutation: A Case Report.

Nurali Ashirov, Iroda Mammadinova, Aidos Moldabekov, Berik Zhetpisbaev, Daniyar Teltayev, Nurzhan Ryskeldiyev, Serik Akshulakov

Open access · goldAbstract readCase Reports
In one paragraph

Article in Medicina (Kaunas, Lithuania), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

7 authors at 1 institution in 1 country.

Nurali AshirovMinimal Invasive Neurosurgery Department, National Centre for Neurosurgery, Astana 010000, Kazakhstan.ORCID 0000-0002-1157-1816
Iroda MammadinovaMinimal Invasive Neurosurgery Department, National Centre for Neurosurgery, Astana 010000, Kazakhstan.ORCID 0000-0002-0427-1751
Aidos MoldabekovBrain Neurosurgery Department, National Centre for Neurosurgery, Astana 010000, Kazakhstan.
Berik ZhetpisbaevDepartment of Pathology, National Centre for Neurosurgery, Astana 010000, Kazakhstan.
Daniyar TeltayevMinimal Invasive Neurosurgery Department, National Centre for Neurosurgery, Astana 010000, Kazakhstan.
Nurzhan RyskeldiyevBrain Neurosurgery Department, National Centre for Neurosurgery, Astana 010000, Kazakhstan.
Serik AkshulakovMinimal Invasive Neurosurgery Department, National Centre for Neurosurgery, Astana 010000, Kazakhstan.
National Research Center for Maternal and Child Health · KZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AstrocytomaBrain NeoplasmsEnchondromatosisGenetic TestingHumansIsocitrate DehydrogenaseMutationIDH1 protein, humanIsocitrate DehydrogenaseastrocytomaIDH-mutationMaffucci syndromemultiple enchondroma

Identifiers

PMID37374260
PMCPMC10302001
OpenAlexW4379056520

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.