Evidence map›Paper›PMID 34205333›Full record

ArticleJournal of clinical medicine2021

Phenotypic Features and Genetic Findings in a Cohort of Italian

Federica Boraldi, Vittoria Murro, Francesco Demetrio Lofaro, Dario Pasquale Mucciolo, Sonia Costa, Laura Pavese, Daniela Quaglino

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Observational
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. A Case Report ofDiagnostics (Basel, Switzerland) · 2021
    Article
  11. 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.

Federica BoraldiDepartment of Life Science, University of Modena and Reggio Emilia, Via Campi 287, 41125 Modena, Italy.ORCID 0000-0002-0277-9017
Vittoria MurroDepartment of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Eye Clinic, Viale Pieraccini 6, 50139 Florence, Italy.
Francesco Demetrio LofaroDepartment of Life Science, University of Modena and Reggio Emilia, Via Campi 287, 41125 Modena, Italy.
Dario Pasquale MuccioloDepartment of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Eye Clinic, Viale Pieraccini 6, 50139 Florence, Italy.
Sonia CostaDepartment of Life Science, University of Modena and Reggio Emilia, Via Campi 287, 41125 Modena, Italy.
Laura PaveseDepartment of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Eye Clinic, Viale Pieraccini 6, 50139 Florence, Italy.
Daniela QuaglinoDepartment of Life Science, University of Modena and Reggio Emilia, Via Campi 287, 41125 Modena, Italy.ORCID 0000-0002-4302-5078

Funding

PXE Italia Odv E96C18000600007
6 · The paper itself

Abstract

background

methodsA retrospective study was performed on 377 PXE patients of Italian origin, clinically evaluated according to the Phenodex Index, who underwent

resultsA total of 117 different

Indexed as

ABCC6atrophycomet lesionpattern dystrophyPhenodexphenotypePXE

Identifiers

PMID34205333
PMCPMC8235548

What OpenQuestion holds

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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.