Evidence map›Paper›PMID 29228108›Full record

ArticleBrain : a journal of neurology2018

DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions.

Leonardo Caporali, Luca Bello, Francesca Tagliavini, Chiara La Morgia, Alessandra Maresca, Lidia Di Vito, Rocco Liguori, Maria Lucia Valentino, Diego Cecchin, Elena Pegoraro and 1 more

Open access · bronzeAbstract readLetterComment
PubMed Publisher
In one paragraph

Article in Brain : a journal of neurology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study.Movement disorders : official journal of the Movement Disorder Society · 2022
    Article
  9. Article
  10. Therapy Prospects for Mitochondrial DNA Maintenance Disorders.International journal of molecular sciences · 2021
    Review
  11. Article
  12. CPEO and Mitochondrial Myopathy in a Patient withCase reports in neurological medicine · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Leonardo CaporaliIRCCS Institute of Neurological Sciences of Bologna, Bellaria Hospital, Bologna, Italy.
Luca BelloDepartment of Neuroscience, University of Padova, Padova, Italy.
Francesca TagliaviniIRCCS Institute of Neurological Sciences of Bologna, Bellaria Hospital, Bologna, Italy.
Chiara La MorgiaIRCCS Institute of Neurological Sciences of Bologna, Bellaria Hospital, Bologna, Italy.
Alessandra MarescaIRCCS Institute of Neurological Sciences of Bologna, Bellaria Hospital, Bologna, Italy.
Lidia Di VitoIRCCS Institute of Neurological Sciences of Bologna, Bellaria Hospital, Bologna, Italy.
Rocco LiguoriIRCCS Institute of Neurological Sciences of Bologna, Bellaria Hospital, Bologna, Italy.
Maria Lucia ValentinoIRCCS Institute of Neurological Sciences of Bologna, Bellaria Hospital, Bologna, Italy.
Diego CecchinNuclear Medicine Unit, Department of Medicine - DIMED, University-Hospital of Padova, Italy.
Elena PegoraroDepartment of Neuroscience, University of Padova, Padova, Italy.
Valerio CarelliIRCCS Institute of Neurological Sciences of Bologna, Bellaria Hospital, Bologna, Italy.
Institute of Neurological Sciences · ITUniversity of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Mitochondrial MyopathiesParkinsonian DisordersAdultDNA, MitochondrialHigh-Throughput Nucleotide SequencingHumansMutationOphthalmoplegia, Chronic Progressive ExternalDNA, Mitochondrial

Identifiers

PMID29228108
OpenAlexW2772674404

What OpenQuestion holds

Textmetadata
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.