Evidence map›Paper›PMID 31873763›Full record

ReviewPediatric radiology2020

Radiographic overlap of recurrent Caffey disease and chronic recurrent multifocal osteomyelitis (CRMO) with considerations of molecular origins.

Teresa Chapman, Sarah J Menashe, Benjamin H Taragin

Abstract readReview
PubMed Publisher
In one paragraph

Review in Pediatric radiology, 2020. 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
0.6field-weighted citation impact, top 29% 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, 10 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Teresa ChapmanDepartment of Radiology, Seattle Children's Hospital, University of Washington School of Medicine, Campus Box 359300, 1959 NE Pacific St., Seattle, WA, 98195, USA. teresa.chapman@seattlechildrens.org.ORCID 0000-0002-6707-0228
Sarah J MenasheDepartment of Radiology, Seattle Children's Hospital, University of Washington School of Medicine, Campus Box 359300, 1959 NE Pacific St., Seattle, WA, 98195, USA.
Benjamin H TaraginDepartment of Pediatric Radiology, Soroka University Medical Center, Ben-Gurion University, Beer Sheva, Israel.
Seattle Children's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Caffey disease, or infantile cortical hyperostosis, classically describes a self-limited inflammatory disorder that presents in the infant with fussiness, focal swelling and sometimes fever. Imaging is conventionally limited to radiography, which shows mild to profound subperiosteal bone formation and sometimes deformity. This disease was not uncommonly diagnosed in the late 20

Indexed as

Bone and BonesChildChild, PreschoolDiagnosis, DifferentialFemaleHumansHyperostosis, Cortical, CongenitalInfantInfant, NewbornMagnetic Resonance ImagingMaleOsteomyelitisRadiographyRecurrenceCaffey diseaseChildrenChronic recurrent multifocal osteomyelitisCOL1A1Infantile cortical hyperostosisRadiographySclerosing bone diseaseSterile osteomyelitis

Identifiers

PMID31873763
OpenAlexW2996699731

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.