Evidence map›Paper›PMID 37274327›Full record

ReviewFrontiers in endocrinology2023

Brain and eye involvement in McCune-Albright Syndrome: clinical and translational insights.

Ilaria Mascioli, Giulia Iapadre, Diletta Ingrosso, Giulio Di Donato, Cosimo Giannini, Vincenzo Salpietro, Francesco Chiarelli, Giovanni Farello

Open access · goldAbstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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 2 institutions in 1 country.

Ilaria MascioliDepartment of Pediatrics, University of Chieti, Chieti, Italy.
Giulia IapadreDepartment of Pediatrics, University of L'Aquila, L'Aquila, Italy.
Diletta IngrossoDepartment of Pediatrics, University of Chieti, Chieti, Italy.
Giulio Di DonatoDepartment of Pediatrics, University of L'Aquila, L'Aquila, Italy.
Cosimo GianniniDepartment of Pediatrics, University of Chieti, Chieti, Italy.
Vincenzo SalpietroDepartment of Pediatrics, University of L'Aquila, L'Aquila, Italy.
Francesco ChiarelliDepartment of Pediatrics, University of Chieti, Chieti, Italy.
Giovanni FarelloDepartment of Pediatrics, University of L'Aquila, L'Aquila, Italy.
University of Chieti-Pescara · ITUniversity of L'Aquila · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

McCune-Albright Syndrome (MAS) is a rare mosaic (post-zygotic) genetic disorder presenting with a broad continuum clinical spectrum. MAS arises from somatic, activating mutations in the

Indexed as

Cushing SyndromeEndocrine System DiseasesFibrous Dysplasia of BoneFibrous Dysplasia, PolyostoticBrainFemaleGTP-Binding Protein alpha Subunits, GsHumansPregnancyGTP-Binding Protein alpha Subunits, Gsbraineyefibrous dysplasia of boneGNASMcCune-Albright Syndrome

Identifiers

PMID37274327
PMCPMC10235602
OpenAlexW4377139000

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.