Evidence map›Paper›PMID 32181031›Full record

ArticleCase reports in neurological medicine2020

Unusual Phenotype and Disease Trajectory in Kearns-Sayre Syndrome.

Josef Finsterer, Michael Winklehner, Claudia Stöllberger, Thomas Hummel

Open access · goldAbstract readCase Reports
In one paragraph

Article in Case reports in neurological medicine, 2020. 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 36% 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, 12 citations in OpenAlex.

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  4. Review
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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 2 institutions in 1 country.

Josef FinstererKrankenanstalt Rudolfstiftung, Messerli Institute, Vienna, Austria.ORCID https://orcid.org/0000-0003-2839-7305
Michael WinklehnerInstitute of Neurology, Medical University of Vienna, Vienna, Austria.
Claudia Stöllberger2nd Medical Department, Krankenanstalt Rudolfstiftung, Vienna, Austria.
Thomas HummelKrankenhaus Stockerau, Stockerau, Austria.
Krankenanstalt Rudolfstiftung der Stadt Wien · ATMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo describe unusual course and unusual phenotypic features in an adult patient with Kearns-Sayre syndrome (KSS).

conclusionsKSS is a multisystem disease, but the number of tissues affected is higher than so far anticipated. KSS should be considered even if core features develop not earlier than in adulthood and if unusual features accompany the presentation.

Identifiers

PMID32181031
PMCPMC7064856
OpenAlexW3007026400

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.