Evidence map›Paper›PMID 35052414›Full record

ReviewGenes2021

Preclinical Research in McArdle Disease: A Review of Research Models and Therapeutic Strategies.

Mónica Villarreal-Salazar, Astrid Brull, Gisela Nogales-Gadea, Antoni L Andreu, Miguel A Martín, Joaquín Arenas, Alfredo Santalla, Alejandro Lucia, John Vissing, Thomas O Krag and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 2021. 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
0.9field-weighted citation impact, top 25% 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. Review
  2. Article
  3. 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

11 authors at 6 institutions in 3 countries.

Mónica Villarreal-SalazarMitochondrial and Neuromuscular Disorders Unit, Vall d'Hebron Institut de Recerca, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain.ORCID 0000-0002-8794-691X
Astrid BrullNeuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0002-3012-451X
Gisela Nogales-GadeaGrup de Recerca en Malalties Neuromusculars i Neuropediàtriques, Department of Neurosciences, Institut d'Investigacio en Ciencies de la Salut Germans Trias i Pujol i Campus Can Ruti, Universitat Autònoma de Barcelona, 08916 Barcelona, Spain.
Antoni L AndreuEATRIS, European Infrastructure for Translational Medicine, 1081 HZ Amsterdam, The Netherlands.
Miguel A MartínCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), 28029 Madrid, Spain.ORCID 0000-0003-4741-772X
Joaquín ArenasCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), 28029 Madrid, Spain.
Alfredo SantallaDepartment of Sport Sciences, Universidad Pablo de Olavide, 41013 Sevilla, Spain.ORCID 0000-0001-9418-0564
Alejandro LuciaFaculty of Sport Sciences, European University, 28670 Madrid, Spain.
John VissingCopenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, University of Copenhagen, DK-2100 Copenhagen, Denmark.
Thomas O KragCopenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, University of Copenhagen, DK-2100 Copenhagen, Denmark.ORCID 0000-0001-9330-668X
Tomàs PinósMitochondrial and Neuromuscular Disorders Unit, Vall d'Hebron Institut de Recerca, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain.
Universitat Autònoma de Barcelona · ESResearch Institute Hospital 12 de Octubre · ESUniversity of Copenhagen · DKNational Institutes of Health · USUniversidad Europea de Madrid · ESUniversidad Pablo de Olavide · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

McArdle disease is an autosomal recessive disorder of muscle glycogen metabolism caused by pathogenic mutations in the

Indexed as

Disease Models, AnimalAnimalsGlycogen Storage Disease Type VHumansMuscle, Skeletalglycogenglycogen phosphorylaseMcArdle diseaseresearch modelstreatments

Identifiers

PMID35052414
PMCPMC8774685
OpenAlexW4200627648

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.