Evidence map›Paper›PMID 42624856›Full record

ArticleNPJ Parkinson's disease2026

Regional reduction of high-energy phosphorus metabolites characterizes the cerebellar subtype of multiple system atrophy.

Jannik Prasuhn, Christina Bodemann, Britt Ebeling, Katharina Reuther, Sinja S Großer, Jan Uter, Julia Henkel, Henrike Hanssen, Norbert Brüggemann

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Jannik PrasuhnSection of Movement Disorders, Department of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany.
Christina BodemannSection of Movement Disorders, Department of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany.
Britt EbelingSection of Movement Disorders, Department of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany.
Katharina ReutherSection of Movement Disorders, Department of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany.
Sinja S GroßerSection of Movement Disorders, Department of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany.
Jan UterSection of Movement Disorders, Department of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany.
Julia HenkelSection of Movement Disorders, Department of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany.
Henrike HanssenSection of Movement Disorders, Department of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany.
Norbert BrüggemannSection of Movement Disorders, Department of Neurology, University Medical Center Schleswig-Holstein, Lübeck, Germany. norbert.brueggemann@uni-luebeck.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple system atrophy (MSA) is a severe neurodegenerative disorder with various underlying pathophysiological features. Mitochondrial dysfunction has been implied as a viable treatment target in patients with MSA. Yet, there is a lack of in-vivo studies examining regional metabolic differences between the Parkinsonian (MSAp) and the cerebellar (MSAc) subtype of MSA. Twenty-four patients with MSA (12 patients with MSAp and 12 patients with MSAc), 24 patients with Parkinson's disease (PD), and 24 age- and sex-matched healthy controls (HCs) underwent clinical evaluations and multimodal neuroimaging, including

Identifiers

PMID42624856
PMCPMC13493920

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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.