Evidence map›Paper›PMID 30424919›Full record

ArticleNeuromuscular disorders : NMD2018

234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8-10 December 2017.

Conrad C Weihl, Bjarne Udd, Michael Hanna, ENMC workshop study group

Abstract readConference Proceedings
In one paragraph

Article in Neuromuscular disorders : NMD, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Genotype‒phenotype correlation in recessive DNAJB4 myopathy.Acta neuropathologica communications · 2024
    Article
  3. Article
  4. Article
  5. 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

4 authors.

Conrad C WeihlDepartment of Neurology, Washington University School of Medicine, Box 8111, 660 South Euclid Avenue, Saint Louis, MO 63110, USA. Electronic address: weihlc@neuro.wustl.edu.
Bjarne UddTampere Neuromuscular Center and Folkhalsan Genetic Institute, Helsinki, Finland.
Michael HannaUCL Institute of Neurology, Queen Square, London, UK.
ENMC workshop study group

Funding

Chaperone Dysfunction in Myopathy: Connecting Yeast Genetics with Mouse ModelsR01AR068797 · NIAMS · WASHINGTON UNIVERSITY · PI TRUE-KROB, HEATHER L, WEIHL, CONRAD C · 2015 to 2025
$6.1M
Clinical and Translational Studies in Muscle DiseaseK24AR073317 · NIAMS · WASHINGTON UNIVERSITY · PI CONRAD C WEIHL · 2018 to 2026
$1.6M
NIAMS NIH HHS K24 AR073317NIAMS NIH HHS R01 AR068797
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

HumansMolecular ChaperonesMuscular DiseasesNetherlandsMolecular Chaperones

Identifiers

PMID30424919
PMCPMC6515901

What OpenQuestion holds

Textmetadata
LicenceTDM
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.