Evidence map›Paper›PMID 30583522›Full record

ArticleJournal of clinical medicine2018

A Novel Mutation in the Stalk Domain of

Massimiliano Filosto, Stefano Cotti Piccinelli, Ilaria Palmieri, Nicola Necchini, Marialuisa Valente, Isabella Zanella, Giorgio Biasiotto, Diego Di Lorenzo, Cristina Cereda, Alessandro Padovani

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of clinical medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. New variants and genotype-phenotype correlation inJournal of medical genetics · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. International journal of molecular sciences · 2021
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Defects in Axonal Transport in Inherited Neuropathies.Journal of neuromuscular diseases · 2019
    Review
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 at 3 institutions in 1 country.

Massimiliano FilostoCenter for Neuromuscular Diseases, Unit of Neurology, ASST Spedali Civili and University of Brescia, 25100 Brescia, Italy. massimiliano.filosto@unibs.it.ORCID 0000-0002-2852-7512
Stefano Cotti PiccinelliCenter for Neuromuscular Diseases, Unit of Neurology, ASST Spedali Civili and University of Brescia, 25100 Brescia, Italy. stefanocottipiccinelli@gmail.com.
Ilaria PalmieriGenomic and Post-Genomic Center, IRCCS Mondino Fundation, 27100 Pavia, Italy. ilaria.palmieri01@universitadipavia.it.
Nicola NecchiniCenter for Neuromuscular Diseases, Unit of Neurology, ASST Spedali Civili and University of Brescia, 25100 Brescia, Italy. nnecchini@gmail.com.
Marialuisa ValenteGenomic and Post-Genomic Center, IRCCS Mondino Fundation, 27100 Pavia, Italy. marialuisa.valente@mondino.it.
Isabella ZanellaDepartment of Molecular and Translational Medicine, University of Brescia, 25100 Brescia, Italy. isabella.zanella@unibs.it.ORCID 0000-0003-3902-3376
Giorgio BiasiottoDepartment of Molecular and Translational Medicine, University of Brescia, 25100 Brescia, Italy. giorgio.biasiotto@unibs.it.
Diego Di LorenzoDepartment of Molecular and Translational Medicine, University of Brescia, 25100 Brescia, Italy. diego.dilorenzo@yahoo.it.
Cristina CeredaGenomic and Post-Genomic Center, IRCCS Mondino Fundation, 27100 Pavia, Italy. cristina.cereda@mondino.it.
Alessandro PadovaniCenter for Neuromuscular Diseases, Unit of Neurology, ASST Spedali Civili and University of Brescia, 25100 Brescia, Italy. alessandro.padovani@unibs.it.
University of Brescia · ITAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · ITCenter for Genomic Science · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ALSaxonal neuropathyhereditary spastic paraplegiasHSPKIF5ASPG10

Identifiers

PMID30583522
PMCPMC6352268
OpenAlexW2906572338

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.