Evidence map›Paper›PMID 34513772›Full record

ArticleFrontiers in pediatrics2021

Case Report: Diffuse Polymicrogyria Associated With a Novel

Fábio Carneiro, Júlia Duarte, Francisco Laranjeira, Sofia Barbosa-Gouveia, María-Luz Couce, Maria José Fonseca

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in pediatrics, 2021. 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
0.9field-weighted citation impact, top 23% 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, 7 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 4 institutions in 2 countries.

Fábio CarneiroNeurology Department, Hospital Garcia de Orta, Almada, Portugal.
Júlia DuarteNeuroradiology Department, Hospital Garcia de Orta, Almada, Portugal.
Francisco LaranjeiraBiochemical Genetics Unit, Centro de Genética Médica Doutor Jacinto Magalhães, Porto, Portugal.
Sofia Barbosa-GouveiaUnit of Diagnosis and Treatment of Congenital Metabolic Diseases, Hospital Clínico Universitario de Santiago de Compostela, Instituto de Investigación Sanitaria de Santiago de Compostela, Centro de Investigación Biomédica en Red de Enfermedades Raras, European Reference Network for Rare Hereditary Metabolic Disorders, Santiago de Compostela, Spain.
María-Luz CouceUnit of Diagnosis and Treatment of Congenital Metabolic Diseases, Hospital Clínico Universitario de Santiago de Compostela, Instituto de Investigación Sanitaria de Santiago de Compostela, Centro de Investigación Biomédica en Red de Enfermedades Raras, European Reference Network for Rare Hereditary Metabolic Disorders, Santiago de Compostela, Spain.
Maria José FonsecaChild Development Centre Torrado da Silva, Hospital Garcia de Orta, Almada, Portugal.
Hospital Garcia de Orta · PTCentre for Biomedical Network Research on Rare Diseases · ESCentro de Genética Clínica · PTInstituto de Investigación Sanitaria de Santiago · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogenic variants of the

Indexed as

ADGRG1bilateral frontoparietal polymicrogyriabilateral generalized polymicrogyriacase reportGPR56polymicrogyria

Identifiers

PMID34513772
PMCPMC8430206
OpenAlexW3196890567

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.