Evidence map›Paper›PMID 30057996›Full record

ArticleActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology2018

Novel mosaic mutation in the dystrophin gene causing distal asymmetric muscle weakness of the upper limbs and dilated cardiomyopathy.

Joana Ribeiro, Olinda Rebelo, Ana Fernández-Marmiesse, Luís Negrão

Open access · greenAbstract readCase Reports
PubMed Full text at PMC
In one paragraph

Article in Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. EMQN best practice guidelines for genetic testing in dystrophinopathies.European journal of human genetics : EJHG · 2020
    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 at 2 institutions in 2 countries.

Joana RibeiroNeuromuscular Disease Unit, Coimbra University and Hospital Centre, Coimbra, Portugal.
Olinda RebeloNeuromuscular Disease Unit, Coimbra University and Hospital Centre, Coimbra, Portugal.
Ana Fernández-MarmiesseUnidad de Diagnóstico y Tratamiento de Enfermedades Metabólicas Congénitas (UDyTEMC), Hospital Clínico Universitario Santiago de Compostela.
Luís NegrãoNeuromuscular Disease Unit, Coimbra University and Hospital Centre, Coimbra, Portugal.
University of Coimbra · PTComplejo Hospitalario Universitario de Santiago · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A group of heterogeneous muscle diseases are caused by dystrophin gene (

Indexed as

Cardiomyopathy, DilatedCodon, NonsenseCreatine KinaseDystrophinElectromyographyHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMosaicismMuscle, SkeletalMuscle WeaknessUpper ExtremityCodon, NonsenseCreatine KinaseDMD protein, humanDystrophindilated cardiomyopathydystrophin genenext generation sequencing

Identifiers

PMID30057996
PMCPMC6060426
OpenAlexW2810552233

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.