Evidence map›Paper›PMID 25988045›Full record

ArticleOxford medical case reports2014

LMNA-related dilated cardiomyopathy.

Tatiyana Vaikhanskaya, Larysa Sivitskaya, Nina Danilenko, Oleg Davydenko, Tatsiyana Kurushka, Irina Sidorenko

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

Article in Oxford medical case reports, 2014. 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
0.6field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Three new cases of dilated cardiomyopathy caused by mutations in LMNA gene.Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology · 2017
    Article
  5. 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

6 authors at 1 institution in 1 country.

Tatiyana VaikhanskayaCardiology , Republican Scientific and Practical Center of Cardiology , Minsk , Belarus.
Larysa SivitskayaCytoplasmic Inheritance , Institute of Genetics and Cytology, National Academy of Sciences , Minsk , Belarus.
Nina DanilenkoCytoplasmic Inheritance , Institute of Genetics and Cytology, National Academy of Sciences , Minsk , Belarus.
Oleg DavydenkoCytoplasmic Inheritance , Institute of Genetics and Cytology, National Academy of Sciences , Minsk , Belarus.
Tatsiyana KurushkaCardiology , Republican Scientific and Practical Center of Cardiology , Minsk , Belarus.
Irina SidorenkoCardiology , Republican Scientific and Practical Center of Cardiology , Minsk , Belarus.
Republican Scientific and Practical Center of Cardiology · BY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A case of idiopathic dilated cardiomyopathy (DCM) that is likely to be associated with LMNA mutation Arg190Pro in a heterozygote is described. The features of DCM in the patient were conduction disorders, cardiac arrhythmias, progressive heart failure and minor musculoskeletal disturbances. We consider that the mutation Arg190Pro contributes to the formation of a weak nuclear lamina and diminishes muscle mechanical stability which is critical during cardiac contraction. The case report illustrates in detail the phenotypic manifestations of the novel LMNA mutation and difficulties in management related to it.

Identifiers

PMID25988045
PMCPMC4369987
OpenAlexW2115058064

What OpenQuestion holds

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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.