Evidence map›Paper›PMID 37362159›Full record

ArticleClinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology2023

A case of papilledema in Camurati-Engelmann disease treated effectively with prednisolone.

Maho Asai, Akira Gomi, Nobuhiro Ibaraki, Hideaki Watanabe, Ichiro Kikkawa, Akihiro Nakamata, Toshihiro Tajima

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 2023. 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
0.3field-weighted citation impact, top 31% 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, 1 citations in OpenAlex.

  1. Article
  2. 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 2 institutions in 1 country.

Maho AsaiDepartment of Pediatrics, Jichi Medical University, Tochigi, Japan.
Akira GomiDepartment of Pediatric Neurosurgery, Jichi Children's Medical Center, Jichi Medical University, Tochigi, Japan.
Nobuhiro IbarakiIbaraki eye clinic, Tochigi, Japan.
Hideaki WatanabeDepartment of Paediatric Orthopaedics and Orthopaedic Surgery, Jichi Children's Medical Center, Tochigi, Japan.
Ichiro KikkawaDepartment of Paediatric Orthopaedics and Orthopaedic Surgery, Jichi Children's Medical Center, Tochigi, Japan.
Akihiro NakamataDepartment of Radiology, Jichi Medical University, Tochigi, Japan.
Toshihiro TajimaDepartment of Pediatrics, Jichi Medical University, Tochigi, Japan.
Jichi Medical University · JPJichi Medical University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Camurati-Engelmann disease (CED) causes bone pain, muscle weakness, and cranial nerve symptoms due to abnormal thickening of the long bones of the limbs and the cortex of the skull. The pathophysiology of CED is a gain-of-function variant of

Indexed as

Camurati-Engelmann diseaseprednisoloneTGFB1visual function

Identifiers

PMID37362159
PMCPMC10288297
OpenAlexW4367276489

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.