Evidence map›Paper›PMID 38792980›Full record

ArticleMedicina (Kaunas, Lithuania)2024

Atypic Retinitis Pigmentosa Clinical Features Associated with a Peculiar CRX Gene Mutation in Italian Patients.

Marco Piergentili, Vito Spagnuolo, Vittoria Murro, Dario Pasquale Mucciolo, Dario Giorgio, Ilaria Passerini, Elisabetta Pelo, Fabrizio Giansanti, Gianni Virgili, Andrea Sodi

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Medicina (Kaunas, Lithuania), 2024. 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
–field-weighted citation impact
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. 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

10 authors.

Marco PiergentiliEye Clinic, Neuromuscular and Sense Organs Department, Careggi University Hospital, 50134 Florence, Italy.ORCID 0000-0001-5713-0461
Vito SpagnuoloEye Clinic, Neuromuscular and Sense Organs Department, Careggi University Hospital, 50134 Florence, Italy.ORCID 0000-0003-0082-8134
Vittoria MurroEye Clinic, Neuromuscular and Sense Organs Department, Careggi University Hospital, 50134 Florence, Italy.
Dario Pasquale MuccioloEye Clinic, Neuromuscular and Sense Organs Department, Careggi University Hospital, 50134 Florence, Italy.
Dario GiorgioEye Clinic, Neuromuscular and Sense Organs Department, Careggi University Hospital, 50134 Florence, Italy.
Ilaria PasseriniDepartment of Genetic Diagnosis, Careggi University Hospital, 50134 Firenze, Italy.
Elisabetta PeloDepartment of Genetic Diagnosis, Careggi University Hospital, 50134 Firenze, Italy.
Fabrizio GiansantiEye Clinic, Neuromuscular and Sense Organs Department, Careggi University Hospital, 50134 Florence, Italy.ORCID 0000-0002-4107-2807
Gianni VirgiliEye Clinic, Neuromuscular and Sense Organs Department, Careggi University Hospital, 50134 Florence, Italy.ORCID 0000-0002-9960-2989
Andrea SodiEye Clinic, Neuromuscular and Sense Organs Department, Careggi University Hospital, 50134 Florence, Italy.

Funding

Italian Ministry of Health, the Tuscany Region and the Sicily Region NET-2016-02363765
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Homeodomain ProteinsRetinitis PigmentosaTrans-ActivatorsAgedElectroretinographyFemaleHumansItalyMaleMutationMutation, MissensePhenotypecone rod homeobox proteinHomeodomain ProteinsTrans-ActivatorsCRX genegenotypelate-onset retinal dystrophypericentral retinitis pigmentosasector retinitis pigmentosa

Identifiers

PMID38792980
PMCPMC11123195

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.