Evidence map›Paper›PMID 27957375›Full record

ArticleCase reports in pediatrics2016

Cardiovascular Malformations in CHARGE Syndrome with DiGeorge Phenotype: Two Case Reports.

Kazushi Yasuda, Eiji Morihana, Naoki Fusazaki, Shiro Ishikawa

Open access · goldAbstract read
In one paragraph

Article in Case reports in pediatrics, 2016. 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
0.2field-weighted citation impact, top 38% 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, 2 citations in OpenAlex.

  1. The Cardiac Neural Crest Cells in Heart Development and Congenital Heart Defects.Journal of cardiovascular development and disease · 2021
    Review
  2. African health sciences · 2018
    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 1 country.

Kazushi YasudaDepartment of Neonatal Cardiology, Fukuoka Children's Hospital, Fukuoka, Japan; Department of Pediatric Cardiology, Fukuoka Children's Hospital, Fukuoka, Japan.ORCID 0000-0002-8739-174X
Eiji MorihanaDepartment of Neonatal Cardiology, Fukuoka Children's Hospital, Fukuoka, Japan.
Naoki FusazakiDepartment of Neonatal Cardiology, Fukuoka Children's Hospital, Fukuoka, Japan.
Shiro IshikawaDepartment of Pediatric Cardiology, Fukuoka Children's Hospital, Fukuoka, Japan.
Fukuoka Children's Hospital and Medical Center for Infectious Diseases · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Both CHARGE syndrome and DiGeorge anomaly are frequently accompanied by cardiovascular malformations. Some specific cardiovascular malformations such as interrupted aortic arch type B and truncus arteriosus are frequently associated with 22q11.2 deletion syndrome, while conotruncal defects and atrioventricular septal defects are overrepresented in patients with CHARGE syndrome.

Identifiers

PMID27957375
PMCPMC5121448
OpenAlexW2553596078

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.