Evidence map›Paper›PMID 29774307›Full record

ArticleActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology2017

Bethlem myopathy in a Portuguese patient - case report.

Ana Inês Martins, Cristin Maarque, Jorge Pinto-Basto, Luis Negrão

Open access · greenAbstract readCase Reports
In one paragraph

Article in Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Segregation of theGenes · 2024
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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 1 institution in 1 country.

Ana Inês MartinsNeuromuscular Disease Unit, Neurology Department, Coimbra University and Hospital Center, Coimbra, Portugal.
Cristin MaarqueNeuromuscular Disease Unit, Neurology Department, Coimbra University and Hospital Center, Coimbra, Portugal.
Jorge Pinto-BastoNeuromuscular Disease Unit, Neurology Department, Coimbra University and Hospital Center, Coimbra, Portugal.
Luis NegrãoNeuromuscular Disease Unit, Neurology Department, Coimbra University and Hospital Center, Coimbra, Portugal.
Hospitais da Universidade de Coimbra · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations of the encoding genes of collagen VI

Indexed as

FingersCollagen Type VIContractureGaitHomozygoteHumansMaleMiddle AgedMuscle WeaknessMuscular DystrophiesMutationPortugalCOL6A2 protein, humanCollagen Type VIBethlem myopathycollagen VIcongenital muscular dystrophy

Identifiers

PMID29774307
PMCPMC5953228
OpenAlexW2776749391

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.