Evidence map›Paper›PMID 33996274›Full record

ArticlePeerJ2021

Function, structure and quality of striated muscles in the lower extremities in patients with late onset Pompe Disease-an MRI study.

Michael Vaeggemose, Rosa Andersen Mencagli, Julie Schjødtz Hansen, Bianca Dräger, Steffen Ringgaard, John Vissing, Henning Andersen

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

Article in PeerJ, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. 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

7 authors at 4 institutions in 2 countries.

Michael VaeggemoseDepartment of Neurology, Aarhus University Hospital, Aarhus N, Denmark.
Rosa Andersen MencagliDepartment of Neurology, Aarhus University Hospital, Aarhus N, Denmark.
Julie Schjødtz HansenDepartment of Neurology, Aarhus University Hospital, Aarhus N, Denmark.
Bianca DrägerDepartment of Sleep Medicine and Neuromuscular Disorders, University Hospital Muenster, Münster, Germany.
Steffen RinggaardMR Research Centre, Aarhus University, Aarhus N, Denmark.
John VissingCopenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Henning AndersenDepartment of Neurology, Aarhus University Hospital, Aarhus N, Denmark.
Aarhus University Hospital · DKAarhus University · DKUniversity Hospital Münster · DEUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPompe Disease (PD) is a rare inherited metabolic myopathy, caused by lysosomal-

methodsThe present study evaluates muscle quality in 10 patients with LOPD receiving treatment with enzyme replacement therapy and in 10 age and gender matched healthy controls applying T

resultsFat fraction of knee flexors (0.15 vs 0.07,

Indexed as

Clinical testsEnzyme replacement therapyFollow-upLate Onset Pompe DiseaseMuscle qualityQuantitative magnetic resonance imaging (mri)

Identifiers

PMID33996274
PMCPMC8106912
OpenAlexW3158553022

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.