Evidence map›Paper›PMID 33564452›Full record

ArticleClinical kidney journal2021

Renal involvement and Strømme syndrome.

Gianluca Caridi, Francesca Lugani, Margherita Lerone, Maria Teresa Divizia, Gian Marco Ghiggeri, Enrico Verrina

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical kidney journal, 2021. 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
0.4field-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, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Biallelic variants in CENPF causing a phenotype distinct from Strømme syndrome.American journal of medical genetics. Part C, Seminars in medical genetics · 2022
    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

6 authors at 1 institution in 1 country.

Gianluca CaridiLaboratory of Molecular Nephrology, IRCCS Istituto Giannina Gaslini, Genova, Italy.ORCID 0000-0001-6700-3001
Francesca LuganiLaboratory of Molecular Nephrology, IRCCS Istituto Giannina Gaslini, Genova, Italy.ORCID 0000-0002-4189-8561
Margherita LeroneLaboratory of Medical Genetics, IRCCS Istituto Giannina Gaslini, Genova, Italy.ORCID 0000-0003-0666-4740
Maria Teresa DiviziaLaboratory of Medical Genetics, IRCCS Istituto Giannina Gaslini, Genova, Italy.
Gian Marco GhiggeriLaboratory of Molecular Nephrology, IRCCS Istituto Giannina Gaslini, Genova, Italy.ORCID 0000-0003-3659-9062
Enrico VerrinaDialysis Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy.ORCID 0000-0002-5178-1949
Istituto Giannina Gaslini · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Strømme syndrome is a rare autosomal recessive congenital disorder involving multiple systems. Centromeric protein F (

Indexed as

centromeric protein F (CENPF)dialysisend-stage renal diseaserare diseaseStrømme syndrome

Identifiers

PMID33564452
PMCPMC7857842
OpenAlexW3002182511

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.