Evidence map›Paper›PMID 31777725›Full record

ArticlePediatric gastroenterology, hepatology & nutrition2019

A Novel

Min Ju Lee, Chae Ri Suh, Jeong Hee Shin, Jee Hyun Lee, Yoon Lee, Baik-Lin Eun, Kee Hwan Yoo, Jung Ok Shim

Open access · hybridAbstract readCase Reports
In one paragraph

Article in Pediatric gastroenterology, hepatology & nutrition, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. A New Aberration in the VPS33B Gene Leads to Full-Symptom ARCS1.The American journal of case reports · 2021
    Article
  4. A Novel Mutation ofCase reports in genetics · 2020
    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

8 authors at 1 institution in 1 country.

Min Ju LeeDepartment of Pediatrics, Korea University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-8900-5953
Chae Ri SuhDepartment of Pediatrics, Korea University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-1975-4323
Jeong Hee ShinDepartment of Pediatrics, Korea University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-3718-968X
Jee Hyun LeeDepartment of Pediatrics, Korea University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-4318-2487
Yoon LeeDepartment of Pediatrics, Korea University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-9521-3575
Baik-Lin EunDepartment of Pediatrics, Korea University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-8735-292X
Kee Hwan YooDepartment of Pediatrics, Korea University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-6490-4293
Jung Ok ShimDepartment of Pediatrics, Korea University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-6449-7819
Korea University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome is a rare autosomal recessive multisystemic disease that is associated with the liver, kidney, skin, and central nervous and musculoskeletal systems. ARC occurs as a result of mutations in the

Indexed as

MutationNeonatal cholestasisVIPARVPS33B

Identifiers

PMID31777725
PMCPMC6856508
OpenAlexW2988332151

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.