Evidence map›Paper›PMID 33334757›Full record

ArticleBMJ case reports2020

Creatine transporter deficiency, an underdiagnosed cause of male intellectual disability.

Neha Jangid, Priyanka Surana, Gajja Salmonos, Vivek Jain

Open access · greenAbstract readCase Reports
In one paragraph

Article in BMJ case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

4 authors at 1 institution in 2 countries.

Neha JangidDepartment of Paediatric Neurology, Santokba Durlabhji Memorial Hospital cum Medical Research Institute, Jaipur, Rajasthan, India.
Priyanka SuranaDepartment of Paediatric Neurology, Santokba Durlabhji Memorial Hospital cum Medical Research Institute, Jaipur, Rajasthan, India.
Gajja SalmonosDepartment of Genetic Metabolic Diseases/Metabolic Unit, VU University Medical Centre Amsterdam, Amsterdam, Noord-Holland, The Netherlands.
Vivek JainDepartment of Paediatric Neurology, Santokba Durlabhji Memorial Hospital cum Medical Research Institute, Jaipur, Rajasthan, India vivekchildneuro@gmail.com.ORCID http://orcid.org/0000-0001-8879-6506
Santokba Durlabhji Memorial hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

X-linked creatine transporter deficiency is caused by the deficiency of the creatine transporter encoded by the

Indexed as

Autistic DisorderBrain Diseases, Metabolic, InbornChild, PreschoolCreatineEpilepsyHemizygoteHumansIntellectual DisabilityMagnetic Resonance SpectroscopyMaleMutationNerve Tissue ProteinsPlasma Membrane Neurotransmitter Transport ProteinsX-Linked Intellectual DisabilityCreatineNerve Tissue ProteinsPlasma Membrane Neurotransmitter Transport ProteinsSLC6A8 protein, humandevelopmental paediatrocsneuro genetics

Identifiers

PMID33334757
PMCPMC7747534
OpenAlexW3112016045

What OpenQuestion holds

Textmetadata
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.