Evidence map›Paper›PMID 32556534›Full record

ArticleJournal of neurology2021

Correction to: Heritable and non-heritable uncommon causes of stroke.

A Bersano, M Kraemer, A Burlina, M Mancuso, J Finsterer, S Sacco, C Salvarani, L Caputi, H Chabriat, S Lesnik Oberstein and 7 more

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

A BersanoCerebrovascular Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy. anna.bersano@gmail.com.
M KraemerDepartment of Neurology Alfried, Krupp-Hospital, Essen, Germany.
A BurlinaNeurological Unit, St. Bassano Hospital, Bassano del Grappa, Italy.
M MancusoDepartment of Clinical and Experimental Medicine, Neurological Institute, University of Pisa, Pisa, Italy.
J FinstererKrankenanstalt Rudolfstiftung, Messerli Institute, Vienna, Austria.
S SaccoDepartment of Neurology, Avezzano Hospital, University of L'Aquila, L'Aquila, Italy.
C SalvaraniUniversity of Modena and Reggio Emilia, and Azienda USL-IRCCS, Reggio Emilia, Italy.
L CaputiCerebrovascular Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
H ChabriatDepartment of Neurology and CERVCO, DHU Neurovasc, INSERM U1141, University of Paris, Paris, France.
S Lesnik ObersteinDepartment of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
A FedericoDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy.
E Tournier-LasserveDepartment of Genetics, Lariboisière Hospital and INSERM U1141, Paris-Diderot University, Paris, France.
D HuntMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, EH4 2XU, UK.
M DichgansInstitute for Stroke and Dementia Research, Klinikum Der Universität München, Munich, Germany.
M ArnoldInserm Centre Bordeaux Population Health (U1219), University of Bordeaux, Bordeaux, France.
S DebetteDepartment of Neurology, INSELSPITAL, University Hospital Bern, Bern, Switzerland.
H S MarkusStroke Research Group, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID32556534

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.